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vab46
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Clinical_trials_anchor-positive-pairs_EmbeddingModel-data2

anchor_id int64 0 8.74k	nctId stringlengths 11 11	chunk_type stringclasses 3 values	block_no int64 1 3	document_id stringlengths 13 13	anchor_type stringclasses 5 values	anchor stringlengths 28 234	positive stringlengths 8 5.04k	chunk_char_length int64 8 5.04k	unique_chunk_identifier stringlengths 64 64	status stringclasses 1 value
0	NCT07661732	title	1	NCT07661732_1	trial_topic_question	What is the focus of the ELITE-HFpEF study?	eHealth Lifestyle Intervention To Enhance Outcomes in HFpEF Randomized Trial Of A Digital Lifestyle Education Strategy In Patients With Heart Failure And Overweight Or Obesity: The ELITE-HFpEF Study	198	d08b7d5b9810dc265979e5d3031190f66ac14fc9a8e315e23f3d6a578ac0d2d0	success
1	NCT07661732	summary	2	NCT07661732_2	study_objective_question	Is there evidence that a digital lifestyle education program improves exercise capacity in adults with heart failure with preserved ejection fraction?	The goal of this clinical trial is to learn if a digital lifestyle education program improves exercise capacity in adults who have heart failure with preserved ejection fraction (HFpEF) and overweight or obesity. HFpEF is a type of heart failure in which the heart muscle is stiff and does not relax well, even though it...	1,202	e4e312b512120909e8d2af05c7e4ca6624ee2f2787c82161cb7468e44e9b5a2b	success
2	NCT07661732	summary	2	NCT07661732_2	clinical_population_question	Are overweight or obese adults with heart failure with preserved ejection fraction being recruited for this clinical trial?	The goal of this clinical trial is to learn if a digital lifestyle education program improves exercise capacity in adults who have heart failure with preserved ejection fraction (HFpEF) and overweight or obesity. HFpEF is a type of heart failure in which the heart muscle is stiff and does not relax well, even though it...	1,202	e4e312b512120909e8d2af05c7e4ca6624ee2f2787c82161cb7468e44e9b5a2b	success
3	NCT07661732	inclusion_criteria	3	NCT07661732_3	patient_profile_question	What are the symptoms consistent with heart failure in this trial?	* Age over 18 years * Body mass index (BMI) over 27 kg/m² * Symptoms consistent with heart failure * Left ventricular ejection fraction (LVEF) of 50% or higher * Elevated NT-proBNP according to the European Society of Cardiology age-adjusted rule-in thresholds: 125 pg/mL or higher if under 50 years, 250 pg/mL or higher...	501	3ca3b2b2bd1be031044984f628e17bb566c6f527061a324fe5bbf389d58e4652	success
4	NCT07661732	inclusion_criteria	3	NCT07661732_3	eligibility_constraint_question	What is the minimum BMI required for inclusion in this clinical trial?	* Age over 18 years * Body mass index (BMI) over 27 kg/m² * Symptoms consistent with heart failure * Left ventricular ejection fraction (LVEF) of 50% or higher * Elevated NT-proBNP according to the European Society of Cardiology age-adjusted rule-in thresholds: 125 pg/mL or higher if under 50 years, 250 pg/mL or higher...	501	3ca3b2b2bd1be031044984f628e17bb566c6f527061a324fe5bbf389d58e4652	success
5	NCT07704034	title	1	NCT07704034_1	trial_topic_question	What is the focus of this clinical trial?	Wearable-Triggered Digital Safety Net for Real-Time Monitoring and Intervention in Leptomeningeal Metastasis	108	8f1e1bde5e487d1aadc4af2ba31319921d9ea0932dc8619afc67b66922aab95a	success
6	NCT07704034	inclusion_criteria	3	NCT07704034_3	patient_profile_question	What is the specific type of metastasis that participants must have?	* Participants must have leptomeningeal metastasis (LMM) diagnosed per clinical, imaging, and/or CSF/cytology criteria (cytology, flow cytometry, or circulating tumor DNA), arising from any solid or hematologic tumor primary. * Participants must be undergoing active anti-cancer therapy (systemic, intrathecal, and/or ra...	1,159	9e18c8a554c89d6cdb998499fb73940fd8097c918b4a703124c00344db7a9635	success
7	NCT07704034	inclusion_criteria	3	NCT07704034_3	eligibility_constraint_question	What is the minimum age requirement for study enrollment?	* Participants must have leptomeningeal metastasis (LMM) diagnosed per clinical, imaging, and/or CSF/cytology criteria (cytology, flow cytometry, or circulating tumor DNA), arising from any solid or hematologic tumor primary. * Participants must be undergoing active anti-cancer therapy (systemic, intrathecal, and/or ra...	1,159	9e18c8a554c89d6cdb998499fb73940fd8097c918b4a703124c00344db7a9635	success
8	NCT07704034	summary	2	NCT07704034_2	study_objective_question	Is this clinical trial investigating the use of consumer Smartwatches for monitoring health in patients with leptomeningeal metastasis?	This research study is for participants diagnosed with leptomeningeal metastasis disease (LMM), a condition where cancer has spread to the fluid and membranes surround the brain and spinal cord. The purpose of this study is to find out whether a consumer Smartwatch can continuously monitor the participant's health and ...	515	7fd34c5543eff871725a7df99e11051bed92afc42ffcc2154bfbf1ed981c011f	success
9	NCT07704034	summary	2	NCT07704034_2	clinical_population_question	Who are the participants being recruited for this clinical trial, specifically those diagnosed with leptomeningeal metastasis disease?	This research study is for participants diagnosed with leptomeningeal metastasis disease (LMM), a condition where cancer has spread to the fluid and membranes surround the brain and spinal cord. The purpose of this study is to find out whether a consumer Smartwatch can continuously monitor the participant's health and ...	515	7fd34c5543eff871725a7df99e11051bed92afc42ffcc2154bfbf1ed981c011f	success
10	NCT07698509	title	1	NCT07698509_1	trial_topic_question	What is the focus of this clinical trial?	Virtual Lifestyle Medicine Group Visits for High Blood Pressure A Scalable, Lifestyle Medicine Intervention for Hypertension Using Virtual Group Shared Medical Appointments	172	b078c8474731ff7351485144fdcc3882e1e7674db8d7bdebb8552399a7dcd906	success
11	NCT07698509	summary	2	NCT07698509_2	clinical_population_question	Who is the target population for this virtual Lifestyle medicine shared medical appointments study?	The purpose of this study is to learn whether virtual Lifestyle medicine shared medical appointments (LMSMAs) can help people better manage their blood pressure and improve their overall health.	194	9afa9188885bd538c7595651e2dd44187bb3be6f67f1ca03012dac4d47eee2f3	success
12	NCT07698509	inclusion_criteria	3	NCT07698509_3	patient_profile_question	What is the current diagnosis of hypertension for this clinical trial?	* Current diagnosis of hypertension (ICD codes I10.0-I14.0 billed within the last 5 years Essential HTN, Essential HTN, Primary HTN) * Currently receives care at a UTPhysicians; Last seen by a PCP at Victory location within the last 1 year. * Able to participate in a virtual format * Willingness to participate and enga...	358	1988ae491d7ef0fb63644d62eafae16c7f5c7e26e45ea89ff15ad96ff5cbf6fb	success
13	NCT07698509	inclusion_criteria	3	NCT07698509_3	eligibility_constraint_question	Must participants have received care at a UTPhysicians within the last year?	* Current diagnosis of hypertension (ICD codes I10.0-I14.0 billed within the last 5 years Essential HTN, Essential HTN, Primary HTN) * Currently receives care at a UTPhysicians; Last seen by a PCP at Victory location within the last 1 year. * Able to participate in a virtual format * Willingness to participate and enga...	358	1988ae491d7ef0fb63644d62eafae16c7f5c7e26e45ea89ff15ad96ff5cbf6fb	success
14	NCT07637097	title	1	NCT07637097_1	trial_topic_question	What is the focus of this clinical trial?	VOCALE LBD: Online Peer Support for Caregivers of People With Lewy Body Dementia Reducing Depression in Family Caregivers of Persons Living With Lewy Body Dementia Through Tailored Asynchronous Online Intervention.	214	d18761eeebddef6b9c9509752dbaffc1b22286a9d81371f56905c7901e4d328d	success
15	NCT07637097	summary	2	NCT07637097_2	clinical_population_question	Who are the family caregivers being targeted in this study?	This study tests whether a tailored, fully asynchronous online group intervention (VOCALE LBD) reduces depression in family caregivers of people with Lewy Body Dementia (LBD), compared to standard educational materials. LBD is the second most common form of degenerative dementia and causes distinct challenges, includin...	1,337	408ec8e976f14317b8149094539dbd38168549c7dcfecf442c81baf9081e208d	success
16	NCT07637097	inclusion_criteria	3	NCT07637097_3	patient_profile_question	Who has a confirmed diagnosis of Lewy Body Dementia (LBD) or LBD mixed pathology?	* Current family member or informal (unpaid) caregiver of a person with a confirmed diagnosis of Lewy Body Dementia (LBD) or LBD mixed pathology * Experiences depressive symptoms as defined by a score of 5 or higher on the Patient Health Questionnaire-9 (PHQ-9) * Able to read, write, and speak English * Has access to a...	488	874051ac9a49833db9775129a47f11e8a362ce9354085a982dc10e19c289509f	success
17	NCT07637097	inclusion_criteria	3	NCT07637097_3	eligibility_constraint_question	What is the minimum score on the Patient Health Questionnaire-9 (PHQ-9) for a caregiver to be eligible?	* Current family member or informal (unpaid) caregiver of a person with a confirmed diagnosis of Lewy Body Dementia (LBD) or LBD mixed pathology * Experiences depressive symptoms as defined by a score of 5 or higher on the Patient Health Questionnaire-9 (PHQ-9) * Able to read, write, and speak English * Has access to a...	488	874051ac9a49833db9775129a47f11e8a362ce9354085a982dc10e19c289509f	success
18	NCT07717671	title	1	NCT07717671_1	trial_topic_question	What is the focus of the VIPPSTAR-G1 clinical trial?	VIPPSTAR-G1 Digital Early Intervention for Visual Impairment VIPPSTAR-G1: A Multicenter Randomized Controlled Trial Evaluating a Caregiver-mediated Digital Intervention to Promote Visual Function and Neurodevelopment in Infants at Risk of/With Visual Impairment	261	49899359709950ab8c0253ea496f26f43ee86d26509011951cda54255b2c9e7e	success
19	NCT07717671	summary	2	NCT07717671_2	clinical_population_question	Who are the participants at risk of or with visual impairment being targeted in the VIPPSTAR-G1 study?	Visual impairment in infancy is associated with significant risks for neurodevelopmental impairment. Early intervention based on enriched visual and multisensory experiences may promote neuroplasticity and improve developmental outcomes, but implementation of intensive interventions in routine clinical practice remains...	1,260	59babb5c86e3d671d1d8748cb542ca4cbfbdab5242f204ef5ceed7e611997bd4	success
20	NCT07717671	inclusion_criteria	3	NCT07717671_3	patient_profile_question	What is the typical gestational age of patients in this trial?	* Gestational age ≤32 weeks OR full-term/newborns\>32 weeks of age with neonatal distress (Apgar ≤5 at 10 minutes) * NAVEG score ≥3 * At least one neurological or neuroimaging abnormality: * 3 abnormal signs at ATNAT neurological examination OR Abnormal cranial ultrasound findings OR Abnormal MRI findings * Age ≤42 ...	382	822de48868e5737606b84d1796af999d8ee20eaf7f0eb486ba8a8e9f44d80ef6	success
21	NCT07717671	inclusion_criteria	3	NCT07717671_3	eligibility_constraint_question	Are patients with a NAVEG score less than 3 eligible for this trial?	* Gestational age ≤32 weeks OR full-term/newborns\>32 weeks of age with neonatal distress (Apgar ≤5 at 10 minutes) * NAVEG score ≥3 * At least one neurological or neuroimaging abnormality: * 3 abnormal signs at ATNAT neurological examination OR Abnormal cranial ultrasound findings OR Abnormal MRI findings * Age ≤42 ...	382	822de48868e5737606b84d1796af999d8ee20eaf7f0eb486ba8a8e9f44d80ef6	success
22	NCT07738224	title	1	NCT07738224_1	trial_topic_question	What is the focus of this clinical trial?	Using the Babble Boot Camp© Speech Therapy Approach With Babies Born Prematurely Babble Boot Camp© for Preterm Infants: A Trial of a Proactive Speech/Language Intervention	171	c11fe7e765449beec8fffafa57eda8fff86c941d61956771d251d8322405a192	success
23	NCT07738224	summary	2	NCT07738224_2	study_objective_question	What speech therapy intervention is being evaluated for its effectiveness in supporting early communication in preterm infants?	Babble Boot Camp focuses on early speech and language development, environmental enrichment and supporting parent-infant interaction with the aim of improving communication outcomes and parental well-being in at risk children. The goal of this clinical trial is to learn if this parent-coaching speech therapy intervent...	1,182	1f57bbebc491ba6120a1a0d3212533569e957298e8c4952ff05446f74d397fff	success
24	NCT07738224	inclusion_criteria	3	NCT07738224_3	patient_profile_question	What is the gestational age criterion for infant participants?	* Infants born \<32 weeks' gestational age (GA) * Infants medically stable and not ventilator dependent at recruitment * Primary language spoken at home is English * Participants able to attend 6 months of telehealth early intervention * Infants less than 5.5 months corrected age	282	ef6346341a5b480c3a3d53071dfcfd257a5c32a6e04f1d748cdc310c74d1e068	success
25	NCT07738224	inclusion_criteria	3	NCT07738224_3	eligibility_constraint_question	Is English proficiency a requirement for telehealth early intervention?	* Infants born \<32 weeks' gestational age (GA) * Infants medically stable and not ventilator dependent at recruitment * Primary language spoken at home is English * Participants able to attend 6 months of telehealth early intervention * Infants less than 5.5 months corrected age	282	ef6346341a5b480c3a3d53071dfcfd257a5c32a6e04f1d748cdc310c74d1e068	success
26	NCT07751458	title	1	NCT07751458_1	trial_topic_question	What is the focus of the WISE Study?	The WISE Study (WhatsApp Intervention for Sleep in the Elderly) The WISE Study (WhatsApp Intervention for Sleep in the Elderly): Targeting Insomnia and Loneliness With a Digital Booklet	185	60b97f6685327928cd101f898fc3c6cfb4495052fb1103bc90658a25eab01b6a	success
27	NCT07751458	summary	2	NCT07751458_2	study_objective_question	What is being studied in this clinical trial?	Sleep hygiene education is an educational effort to teach healthy sleep habits and behaviors to improve sleep quality, duration, and regularity naturally without the use of medication; however, this approach has not been established in Indonesia. This study aims to establish a sleep hygiene education care model among l...	1,514	50760d5f34206056a70babcb8528f211e05707e524e2c28178609cf8d00c50ed	success
28	NCT07751458	summary	2	NCT07751458_2	clinical_population_question	Who are the participants targeted by this study?	Sleep hygiene education is an educational effort to teach healthy sleep habits and behaviors to improve sleep quality, duration, and regularity naturally without the use of medication; however, this approach has not been established in Indonesia. This study aims to establish a sleep hygiene education care model among l...	1,514	50760d5f34206056a70babcb8528f211e05707e524e2c28178609cf8d00c50ed	success
29	NCT07751458	inclusion_criteria	3	NCT07751458_3	patient_profile_question	What is the primary clinical phenotype of interest in this trial?	* Elderly individuals diagnosed with loneliness * Reported experiencing sleep disturbances in the past 2 weeks, either continuously or intermittently * Experiencing insomnia with a total score of ≥ 8 on the Indonesian version of the Insomnia Severity Index (ISI) during screening * Able to communicate in Indonesian	317	469f1a88cb084bd0c08d9c050f62214918c05760602fcf0cc3e1408f894587df	success
30	NCT07751458	inclusion_criteria	3	NCT07751458_3	eligibility_constraint_question	What is the minimum score on the Indonesian version of the Insomnia Severity Index required for eligibility?	* Elderly individuals diagnosed with loneliness * Reported experiencing sleep disturbances in the past 2 weeks, either continuously or intermittently * Experiencing insomnia with a total score of ≥ 8 on the Indonesian version of the Insomnia Severity Index (ISI) during screening * Able to communicate in Indonesian	317	469f1a88cb084bd0c08d9c050f62214918c05760602fcf0cc3e1408f894587df	success
31	NCT07711301	title	1	NCT07711301_1	trial_topic_question	What is the focus of The Science Tooth Fairy clinical trial?	The Science Tooth Fairy: A Randomized Trial of a Storytelling-Based Educational Intervention to Promote Primary Tooth Donation in a Pediatric Setting Tooth Book Evaluation	171	e8c689a3180f95a9d8f92ddf0c4a7b4a3b56f3a83ff5739a12ae7dd23d9137ca	success
32	NCT07711301	summary	2	NCT07711301_2	study_objective_question	What is being studied in this clinical trial?	Study Overview Primary ("baby") teeth are unique biological samples because they can permanently store information about a child's early life health and development. While donating baby teeth to scientific research is painless and simple, researchers often face challenges collecting them. Past studies show that donatio...	3,101	38e46cee7b8a1a8fd9c936dba53baff1286f4733b84e46d191753969138835c5	success
33	NCT07711301	summary	2	NCT07711301_2	clinical_population_question	Who are the participants in this study, and what is their age range?	Study Overview Primary ("baby") teeth are unique biological samples because they can permanently store information about a child's early life health and development. While donating baby teeth to scientific research is painless and simple, researchers often face challenges collecting them. Past studies show that donatio...	3,101	38e46cee7b8a1a8fd9c936dba53baff1286f4733b84e46d191753969138835c5	success
34	NCT07711301	inclusion_criteria	3	NCT07711301_3	patient_profile_question	What is the age range for the children participating in this clinical trial?	* Biological or non-biological parents (e.g., legal caregivers or guardians) of children aged 4-10 years	106	c3b5edd88ecfd24732e33997abb182d0a4e69f68de8fa42cc56fa1a1e8310feb	success
35	NCT07711301	inclusion_criteria	3	NCT07711301_3	eligibility_constraint_question	Are biological parents eligible to participate in this clinical trial?	* Biological or non-biological parents (e.g., legal caregivers or guardians) of children aged 4-10 years	106	c3b5edd88ecfd24732e33997abb182d0a4e69f68de8fa42cc56fa1a1e8310feb	success
36	NCT07690605	title	1	NCT07690605_1	trial_topic_question	What is the focus of this clinical trial?	The Genomic and Well-Being Impacts of an Extraverted Behavior Intervention	74	e66af89c57a4d56659d8425266d78c11919acf056931a9779df21ae74bfaac53	success
37	NCT07690605	summary	2	NCT07690605_2	clinical_population_question	Who are the participants in this study, and what is their focus?	8-week randomized intervention (with 3-month follow-up) that examines the impact of increased sociable behavior on emotional well-being and immune health profile	161	141e9b5c6b7b0d2607af85e83bafce5fcbfaf1129c4aa6f5053e8c3085490532	success
38	NCT07690605	inclusion_criteria	3	NCT07690605_3	patient_profile_question	What is the minimum age requirement for trial participants?	* Age 18 or older	19	87e817eca50c9e90a2923918b9d0c49897f17b62248a289e1ae164e3c84c9dd4	success
39	NCT07690605	inclusion_criteria	3	NCT07690605_3	eligibility_constraint_question	Is there an upper age limit for patients to be eligible for this clinical trial?	* Age 18 or older	19	87e817eca50c9e90a2923918b9d0c49897f17b62248a289e1ae164e3c84c9dd4	success
40	NCT07755631	title	1	NCT07755631_1	trial_topic_question	What is the focus of the BASIC-S Feasibility Study?	The BASIC-S Feasibility Study for Vascular Risk Reduction Piloting an Integrated Lifestyle Intervention for Vascular Risk Reduction: The BASIC-S Feasibility Study	162	f3b1971b88906d275d18b295471c8b794730e22ab6e7f47eb6a2812f07ef747b	success
41	NCT07755631	summary	2	NCT07755631_2	study_objective_question	What lifestyle changes is this study evaluating for reducing vascular risk factors?	Vascular risk factors drive stroke, heart disease, and dementia, but translating lifestyle guidelines into routine clinical care remains challenging. To address this, we developed the BASIC-S framework, targeting Blood pressure, Activity, Sleep, Interaction (socially), Consumption (nutrition), and Support using partner...	1,051	7a5a191f72b8118e1f068238f389fc5cb9196b19cc156a7610af55deed0c7332	success
42	NCT07755631	summary	2	NCT07755631_2	clinical_population_question	Who are the participants in this cluster-randomized pilot trial?	Vascular risk factors drive stroke, heart disease, and dementia, but translating lifestyle guidelines into routine clinical care remains challenging. To address this, we developed the BASIC-S framework, targeting Blood pressure, Activity, Sleep, Interaction (socially), Consumption (nutrition), and Support using partner...	1,051	7a5a191f72b8118e1f068238f389fc5cb9196b19cc156a7610af55deed0c7332	success
43	NCT07755631	inclusion_criteria	3	NCT07755631_3	patient_profile_question	Are participants in this clinical trial healthcare workers?	* Adults aged 18 years and older currently employed at or recently retired from the London Health Sciences Centre (LHSC) or Western University (with an operational focus on pre-retirees aged 50 years and older). * Spouse or cohabitating partner of an enrolled primary participant (partner enrollment is optional but stro...	566	e9a1a31395ef6c1d04f4916ffd90733fb3baf6e1d74c5ae30c117af1f460f79e	success
44	NCT07755631	inclusion_criteria	3	NCT07755631_3	eligibility_constraint_question	Is age a requirement for enrolling in this study?	* Adults aged 18 years and older currently employed at or recently retired from the London Health Sciences Centre (LHSC) or Western University (with an operational focus on pre-retirees aged 50 years and older). * Spouse or cohabitating partner of an enrolled primary participant (partner enrollment is optional but stro...	566	e9a1a31395ef6c1d04f4916ffd90733fb3baf6e1d74c5ae30c117af1f460f79e	success
45	NCT07666139	title	1	NCT07666139_1	trial_topic_question	What is the focus of the CARES Study?	The 'Comprehensive Adherence Resource and Empowerment Support' (CARES) Study Adapting the 'Comprehensive Adherence Resource and Empowerment Support' Intervention for Multiple PrEP Methods Among Adolescent Girls and Young Women in South Africa and Zimbabwe	255	2342f29e6ca64a2257a72a433c1fcced26980c1276138c0f714a07bd0f939085	success
46	NCT07666139	summary	2	NCT07666139_2	study_objective_question	What is being studied in this clinical trial?	The primary aim of this study is to adapt the Comprehensive Adherence Resource and Empowerment Support (CARES) intervention to support adolescent girls and young women (AGYW) aged 16-24 in Zimbabwe and South Africa in effectively using various forms of pre-exposure prophylaxis (PrEP), specifically oral, ring, and injec...	1,154	6af49faab00ad5f1f5cf6fceef5c1672e1a5af0eeb4e4388928789badfc044d0	success
47	NCT07666139	summary	2	NCT07666139_2	clinical_population_question	Who is the target population for this study?	The primary aim of this study is to adapt the Comprehensive Adherence Resource and Empowerment Support (CARES) intervention to support adolescent girls and young women (AGYW) aged 16-24 in Zimbabwe and South Africa in effectively using various forms of pre-exposure prophylaxis (PrEP), specifically oral, ring, and injec...	1,154	6af49faab00ad5f1f5cf6fceef5c1672e1a5af0eeb4e4388928789badfc044d0	success
48	NCT07666139	inclusion_criteria	3	NCT07666139_3	patient_profile_question	What age group is targeted in this clinical trial?	Aim 2: Inclusion (AGYW): * age 16-24 years (in Zimbabwe, participants aged 16 to 17 years must meet the legal criteria for emancipation to be eligible) * has initiated PrEP during the study, or no more than 6 months before the study initiation date (for LEN PrEP), or no more than 3 months before the study initiation ...	658	76fd53b8b53fdc586ae18352352b4d7d3dcbad72b1814c42514ae0f79bb11f9a	success
49	NCT07666139	inclusion_criteria	3	NCT07666139_3	eligibility_constraint_question	What are the requirements for participants who have initiated PrEP before the study initiation date?	Aim 2: Inclusion (AGYW): * age 16-24 years (in Zimbabwe, participants aged 16 to 17 years must meet the legal criteria for emancipation to be eligible) * has initiated PrEP during the study, or no more than 6 months before the study initiation date (for LEN PrEP), or no more than 3 months before the study initiation ...	658	76fd53b8b53fdc586ae18352352b4d7d3dcbad72b1814c42514ae0f79bb11f9a	success
50	NCT07695818	title	1	NCT07695818_1	trial_topic_question	What is the focus of this clinical trial?	Testing and Evaluation of the Returning to the Land Intervention to Address and Prevent Substance Misuse	104	36aa3b9d245abc3dd06a177b7be1ac5fb0052e6f63f0430addd9d9ad765d03c4	success
51	NCT07695818	summary	2	NCT07695818_2	clinical_population_question	Who is the target population for this study?	This study aims to test the Returning to the Land intervention in partnership with a tribal community. The program is designed to address caregiver substance use and child emotional and behavioral development.	209	42bdb8d8391054410fbf5750b31bf5d840690161d2b432bb628cdda550b96433	success
52	NCT07695818	inclusion_criteria	3	NCT07695818_3	patient_profile_question	What is the age range of eligible participants in this clinical trial?	* Reside on or near the Rocky Boy Reservation (\~50-mile round trip); * Aged 14-19 years; * Parent or primary caregiver to at least one child who will be age 1-5 years at the start of the intervention.	203	40efe526612cd1d8e8804bf7cf77145d777f764833841416e2c39da74ef91252	success
53	NCT07695818	inclusion_criteria	3	NCT07695818_3	eligibility_constraint_question	Do participants need to reside on or near the Rocky Boy Reservation to be eligible for this study?	* Reside on or near the Rocky Boy Reservation (\~50-mile round trip); * Aged 14-19 years; * Parent or primary caregiver to at least one child who will be age 1-5 years at the start of the intervention.	203	40efe526612cd1d8e8804bf7cf77145d777f764833841416e2c39da74ef91252	success
54	NCT07748780	title	1	NCT07748780_1	trial_topic_question	What is the focus of this clinical trial?	Testing a Blended Social-Communication and Social-Emotional Intervention for Autistic Toddlers	94	aa5150c1908e3e2ff8c75920b41e72ac58ffc764e5ccaf008ae86dea4f781e14	success
55	NCT07748780	summary	2	NCT07748780_2	clinical_population_question	What population of autistic toddlers is targeted by this study?	Autistic toddlers often need support to develop both social-communication and social-emotional skills. Social communication (such as making requests or sharing attention) is usually addressed in early intervention, but social-emotional needs (such as expressing feelings or learning to cope with frustration) are often o...	1,448	dbfdfe652f0857db27b3c8fe0e504b0951dccca0df349e06a018c38252ea14ea	success
56	NCT07748780	inclusion_criteria	3	NCT07748780_3	patient_profile_question	What is the age criterion for participants?	* Under 36 months of age at enrollment. * Has a clinical diagnosis of autism. * Is currently receiving services through Part C Early Intervention (EI). * Able to participate in natural caregiver-child routines and play activities. * At least one primary caregiver is available and willing to participate in weekly coach...	697	1e7a044e96fb000760100e2f5273a7530fc1dd036cc21b8aaf33f1c119aa75ed	success
57	NCT07748780	inclusion_criteria	3	NCT07748780_3	eligibility_constraint_question	What is the requirement for caregiver involvement in this clinical trial?	* Under 36 months of age at enrollment. * Has a clinical diagnosis of autism. * Is currently receiving services through Part C Early Intervention (EI). * Able to participate in natural caregiver-child routines and play activities. * At least one primary caregiver is available and willing to participate in weekly coach...	697	1e7a044e96fb000760100e2f5273a7530fc1dd036cc21b8aaf33f1c119aa75ed	success
58	NCT07711730	title	1	NCT07711730_1	trial_topic_question	What is the focus of this clinical trial?	Telecare-Mediated Psychosocial and Cognitive Intervention for Children and Adolescents With Limb-Girdle Muscular Dystrophy	122	c3f73f53b129a6d5c89003b63dcec14466ee7d0b673978689307b5d112245b91	success
59	NCT07711730	summary	2	NCT07711730_2	clinical_population_question	Who are the participants in this study?	This clinical trial aims to evaluate the efficacy of a telecare-mediated psychosocial and cognitive intervention for children and adolescents aged 7 to 17 with limb-girdle muscular dystrophy. This group-based intervention (comprising 5 participants) consists of 12 weekly one-hour sessions. The objective of the interven...	580	85602c7339cdce3a86ebd29bb9b46438857162d2fb3cc0861dec2a8890711ad4	success
60	NCT07711730	inclusion_criteria	3	NCT07711730_3	patient_profile_question	What is the specific muscle disorder being studied in this clinical trial?	* To be diagnosed with limb-girdle muscular dystrophy * Being between 7 and 17 years old * Having signed an informed consent form through their legal guardians prior to participation in the study * Having Spanish as one of their main languages * Having access to a computer (with a camera, microphone and speakers integr...	388	83688a3f8f8ddbcad92291be849d65c20ded6f782fd18bd2c4ce64f52cebb225	success
61	NCT07711730	inclusion_criteria	3	NCT07711730_3	eligibility_constraint_question	What is the age range for participants in this study?	* To be diagnosed with limb-girdle muscular dystrophy * Being between 7 and 17 years old * Having signed an informed consent form through their legal guardians prior to participation in the study * Having Spanish as one of their main languages * Having access to a computer (with a camera, microphone and speakers integr...	388	83688a3f8f8ddbcad92291be849d65c20ded6f782fd18bd2c4ce64f52cebb225	success
62	NCT07724158	title	1	NCT07724158_1	trial_topic_question	What is the focus of this clinical trial?	Target Physiotherapy Versus Exercise Support Intervention for Bladder-bowel Dysfunction in Adolescents With Obesity	115	96dbc8d9fcd54f9170f1c1240c76a189bd063209b2a4400d957a4ca78e29bbd0	success
63	NCT07724158	summary	2	NCT07724158_2	study_objective_question	What interventions are being tested to improve bladder and bowel symptoms in adolescents with obesity?	Bladder and bowel dysfunction (BBD) is a common condition that includes problems such as urinary urgency, daytime urinary incontinence, bedwetting, constipation, or difficulties emptying the bladder or bowel. These symptoms can negatively affect quality of life, emotional well-being, school participation, and social re...	2,499	6f2a88a3168db0fe2edc809ff4246a9a5379cdded1d8d4333fb09955a171b788	success
64	NCT07724158	summary	2	NCT07724158_2	clinical_population_question	Which adolescents with obesity will be included in this study?	Bladder and bowel dysfunction (BBD) is a common condition that includes problems such as urinary urgency, daytime urinary incontinence, bedwetting, constipation, or difficulties emptying the bladder or bowel. These symptoms can negatively affect quality of life, emotional well-being, school participation, and social re...	2,499	6f2a88a3168db0fe2edc809ff4246a9a5379cdded1d8d4333fb09955a171b788	success
65	NCT07724158	inclusion_criteria	3	NCT07724158_3	patient_profile_question	What is the age range for adolescents in this clinical trial?	* Male or female adolescents aged 13 to 18 years. * Obesity defined as BMI z-score ≥2, according to the WHO growth reference for school-aged children and adolescents. * Currently receiving obesity treatment at the Pediatric Outpatient Clinic, Department of Pediatrics, Hospital de Santa Maria, Unidade Local de Saúde de ...	542	57a0c1f0d7126a14bea030fcae1e2d92caf77ef0ac3e21114e80687e6942e265	success
66	NCT07724158	inclusion_criteria	3	NCT07724158_3	eligibility_constraint_question	What is the BMI z-score threshold for obesity eligibility in this study?	* Male or female adolescents aged 13 to 18 years. * Obesity defined as BMI z-score ≥2, according to the WHO growth reference for school-aged children and adolescents. * Currently receiving obesity treatment at the Pediatric Outpatient Clinic, Department of Pediatrics, Hospital de Santa Maria, Unidade Local de Saúde de ...	542	57a0c1f0d7126a14bea030fcae1e2d92caf77ef0ac3e21114e80687e6942e265	success
67	NCT07674212	title	1	NCT07674212_1	trial_topic_question	What is the focus of the Take5Care+ clinical trial?	Take5Care+: A Self-management Educational Intervention Take5Care+: A Self-management Educational Intervention to Support the Haematology Patients' Journey Following a Neoplastic Diagnosis.	188	58251a2c11481cd1b9290223566f5ba382b8a3cb8decdf9e66194ab456cd35b1	success
68	NCT07674212	summary	2	NCT07674212_2	study_objective_question	What is being studied in this clinical trial?	Patients who are diagnosed with haematological malignancies may feel that they have little or no control over their health which can be distressing. However, a diagnosis can also be the opportunity for a "teachable moment" during which patients are more likely to open to behaviour change, which can positively impact on...	1,923	2f5782eb419cc91dbca24bd26f1cb16f212421f778e8a7395847391d64062bd4	success
69	NCT07674212	summary	2	NCT07674212_2	clinical_population_question	Who are the participants in this study?	Patients who are diagnosed with haematological malignancies may feel that they have little or no control over their health which can be distressing. However, a diagnosis can also be the opportunity for a "teachable moment" during which patients are more likely to open to behaviour change, which can positively impact on...	1,923	2f5782eb419cc91dbca24bd26f1cb16f212421f778e8a7395847391d64062bd4	success
70	NCT07674212	inclusion_criteria	3	NCT07674212_3	patient_profile_question	What conditions are patients diagnosed with within the last 3 months?	* 18 years or older. * Have been diagnosed within the last 3 months with one of the eligible conditions listed in Table 1. * Be managed with either: * Active monitoring, or * Non-intensive oral therapy, defined as outpatient oral regimens that do not require inpatient initiation and have lower expected toxicity (e.g...	550	b18fd8257766de6e511754a7887f5656ad40e1cf920c7055dbb6cc1d5d4deda3	success
71	NCT07674212	inclusion_criteria	3	NCT07674212_3	eligibility_constraint_question	What is the minimum ECOG Performance Status required for trial eligibility?	* 18 years or older. * Have been diagnosed within the last 3 months with one of the eligible conditions listed in Table 1. * Be managed with either: * Active monitoring, or * Non-intensive oral therapy, defined as outpatient oral regimens that do not require inpatient initiation and have lower expected toxicity (e.g...	550	b18fd8257766de6e511754a7887f5656ad40e1cf920c7055dbb6cc1d5d4deda3	success
72	NCT07751185	title	1	NCT07751185_1	trial_topic_question	What is the focus of the SHINE clinical trial?	Support and Healing Intervention for Adolescents With a Parent Diagnosed With Cancer (SHINE) Support and Healing Intervention for Navigating Parental Cancer Experiences (SHINE): A Mixed-Methods Study to Develop and Pilot-Test a Family-Centered Psychosocial Intervention for Adolescents With a Parent Diagnosed With Cance...	321	8a5a207f622cc5dc97c5c6e8bb10f59224975e322ae4cee7ee4b05772debd832	success
73	NCT07751185	summary	2	NCT07751185_2	study_objective_question	What family-centered program is being developed to support adolescents whose parent has been diagnosed with cancer?	e purpose of this study is to develop and evaluate SHINE (Support and Healing Intervention for Navigating Parental Cancer Experiences), a family-centered program designed to support adolescents whose parent has been diagnosed with cancer. The study has two phases. In the first phase, parents and adolescents will parti...	1,189	8324aa1901b568196dda774c53c2817d71180d036ce05a3cb508534ec89de733	success
74	NCT07751185	summary	2	NCT07751185_2	clinical_population_question	Who are the participants in this study, and what is their specific experience or situation?	e purpose of this study is to develop and evaluate SHINE (Support and Healing Intervention for Navigating Parental Cancer Experiences), a family-centered program designed to support adolescents whose parent has been diagnosed with cancer. The study has two phases. In the first phase, parents and adolescents will parti...	1,189	8324aa1901b568196dda774c53c2817d71180d036ce05a3cb508534ec89de733	success
75	NCT07751185	inclusion_criteria	3	NCT07751185_3	patient_profile_question	What is the cancer stage for the participating adolescents?	Parent or caregiver aged 18 years or older with a documented diagnosis of Stage I-IV (or equivalent) cancer. Parent or caregiver has at least one adolescent child between the ages of 10 and 17 years living in the household. Parent/caregiver and adolescent are able to communicate in English or Spanish. Parent or careg...	552	d4983022fd5997407ff965851213c9d2edc82a7945b630eef92e0cfad5547c53	success
76	NCT07751185	inclusion_criteria	3	NCT07751185_3	eligibility_constraint_question	What is the age range of the adolescent children involved in this clinical trial?	Parent or caregiver aged 18 years or older with a documented diagnosis of Stage I-IV (or equivalent) cancer. Parent or caregiver has at least one adolescent child between the ages of 10 and 17 years living in the household. Parent/caregiver and adolescent are able to communicate in English or Spanish. Parent or careg...	552	d4983022fd5997407ff965851213c9d2edc82a7945b630eef92e0cfad5547c53	success
77	NCT07717320	title	1	NCT07717320_1	trial_topic_question	What is the focus of this clinical trial in Panama?	Suicidal Risk in Adults in Panama: Validation of a Clinical Intervention Protocol	81	6c73d32b0d01f2601a4d2f91347612e9ca7ff5d7e9ef0e5b8bd69889794754e5	success
78	NCT07717320	summary	2	NCT07717320_2	study_objective_question	What is being studied or evaluated in this clinical trial?	This study aims to validate MBT as an effective and viable intervention for implementation in public health services, with the potential to directly impact suicide prevention policies in the region.	198	5fb06f8bf59ebc451fbae9eda662a4121adabe3e18b06a769a69a0dd76fdd341	success
79	NCT07717320	summary	2	NCT07717320_2	clinical_population_question	Who or what population is the focus of this suicide prevention study?	This study aims to validate MBT as an effective and viable intervention for implementation in public health services, with the potential to directly impact suicide prevention policies in the region.	198	5fb06f8bf59ebc451fbae9eda662a4121adabe3e18b06a769a69a0dd76fdd341	success
80	NCT07717320	inclusion_criteria	3	NCT07717320_3	patient_profile_question	What is the patient's mental health status being evaluated for?	* Age and consent * Presence of suicidal ideation or active behavior in the last month, assessed using the C-SSRS (e.g., intentional ideation, plan, or preparatory behavior) * Depressive or anxious symptoms (Score ≥ 10 on the PHQ-9, indicating at least moderate depressive symptoms, or Score ≥ 10 on the GAD-7, suggestin...	461	551aef08e472c0daedb426e2572a566880ee1c9cf95c2d9459765408bf05fbc6	success
81	NCT07717320	inclusion_criteria	3	NCT07717320_3	eligibility_constraint_question	At what age range are patients eligible to participate in this clinical trial?	* Age and consent * Presence of suicidal ideation or active behavior in the last month, assessed using the C-SSRS (e.g., intentional ideation, plan, or preparatory behavior) * Depressive or anxious symptoms (Score ≥ 10 on the PHQ-9, indicating at least moderate depressive symptoms, or Score ≥ 10 on the GAD-7, suggestin...	461	551aef08e472c0daedb426e2572a566880ee1c9cf95c2d9459765408bf05fbc6	success
82	NCT07710001	title	1	NCT07710001_1	trial_topic_question	What is the focus of this clinical trial?	Study on Influencing Factors and Intervention of Silent Aspiration After Heart Valve Operation in Elderly Patients	114	0fb3a1c47625ba7b1cd9a5fa2265ccf48e4fb4d6b5ea52b3f8c6a27cecf7dc74	success
83	NCT07710001	summary	2	NCT07710001_2	clinical_population_question	Who are the patients being studied in this trial?	Objective To investigate the safety and effectiveness of interference electrical stimulation in the prevention of silent aspiration after heart valve surgery in elderly patients. Silent aspiration was diagnosed when either pepsin level \>200 ng/ml or α-amylase level \>1685 U/L was detected in airway secretions.	312	e1f371404256cffca36a721197f596e5c3b712df2618f0f725afe28e17a3a796	success
84	NCT07710001	inclusion_criteria	3	NCT07710001_3	patient_profile_question	What is the patient's cardiac function classification?	* Simple valve surgery * Age ≥60 years old * NYHA cardiac function Grade II-III * ASA Grade II-III * No dysphagia screened by SSA before surgery	146	2853bc0dd85ccab7617fad7fb2c803b53f14dff43b1ed196ac3f2664f91e1d21	success
85	NCT07710001	inclusion_criteria	3	NCT07710001_3	eligibility_constraint_question	Is the patient at least 60 years old?	* Simple valve surgery * Age ≥60 years old * NYHA cardiac function Grade II-III * ASA Grade II-III * No dysphagia screened by SSA before surgery	146	2853bc0dd85ccab7617fad7fb2c803b53f14dff43b1ed196ac3f2664f91e1d21	success
86	NCT07689799	title	1	NCT07689799_1	trial_topic_question	What is the focus of this clinical trial in Saudi Arabia?	Structured Leadership Intervention for Nurses in Saudi Arabia. Effects of a Structured Leadership Intervention on Nursing Work Environment, Job Satisfaction, and Turnover Intentions: A Randomized Controlled Trial.	213	e3292ca0a0807a44a2e7e37192566326330a175907d9a4210c3ec42480629c2d	success
87	NCT07689799	summary	2	NCT07689799_2	study_objective_question	What is being studied in this clinical trial?	This study is a randomized controlled trial designed to evaluate the effectiveness of a structured transformational leadership educational program on nurses' work environment, job satisfaction, and turnover intentions in acute care hospitals in Saudi Arabia.	258	5ac0e027a1d0cfe8d64f158346a4d398650e81e41fac093f703b34d315a791e2	success
88	NCT07689799	summary	2	NCT07689799_2	clinical_population_question	Who are the participants in this study, specifically regarding their work environment and location?	This study is a randomized controlled trial designed to evaluate the effectiveness of a structured transformational leadership educational program on nurses' work environment, job satisfaction, and turnover intentions in acute care hospitals in Saudi Arabia.	258	5ac0e027a1d0cfe8d64f158346a4d398650e81e41fac093f703b34d315a791e2	success
89	NCT07689799	inclusion_criteria	3	NCT07689799_3	patient_profile_question	What is the typical professional background of participants in this trial?	* Registered nurses with 6 or more months of clinical experience. * Full-time employment in inpatient units.	110	37f57daa99b263cf5ac9a17a17b9be52411eff9df5ea6f12ab956d1ef25887bb	success
90	NCT07689799	inclusion_criteria	3	NCT07689799_3	eligibility_constraint_question	Is full-time employment in inpatient units a requirement for participation in this clinical trial?	* Registered nurses with 6 or more months of clinical experience. * Full-time employment in inpatient units.	110	37f57daa99b263cf5ac9a17a17b9be52411eff9df5ea6f12ab956d1ef25887bb	success
91	NCT07737912	title	1	NCT07737912_1	trial_topic_question	What is the focus of the SpinePal Open Pilot clinical trial?	SpinePal Open Pilot User-Centered Development of an App-Based Cognitive-Behavioral Intervention to Reduce Persistent Opioid Use and Opioid Related Problems Following Spine Surgery	179	d98fd74ce37fa08f5290fa00a02a7ca6a8863ee86b567edf9b9bf664921a227c	success
92	NCT07737912	summary	2	NCT07737912_2	study_objective_question	What is being studied in this clinical trial regarding patients undergoing spine surgery?	SpinePal is a self-guided digital intervention developed for patients undergoing spine surgery. The goal of this study is to learn if SpinePal is acceptable to people undergoing spine surgery. The main questions the investigators aim to answer are: * Is the SpinePal platform considered usable and acceptable by people ...	709	740dea15e7a26c92d4949564e6a7a23753a72512b4f2dcbaf887dfd5e38f4bda	success
93	NCT07737912	inclusion_criteria	3	NCT07737912_3	patient_profile_question	Who is eligible for this clinical trial?	* 18 years or older * English-speaking * Able and willing to provide informed consent * Scheduled for lumbar or cervical fusion surgery at least 2 weeks from the date of enrollment * Owns a smartphone with reliable internet and/or data access * Willing to engage with SpinePal and physiological monitoring via wrist-worn...	329	3bc5e5827d9aba100b525bc964cf7f0640ca29a41332c7aae004a27705491bf2	success
94	NCT07737912	inclusion_criteria	3	NCT07737912_3	eligibility_constraint_question	What are the smartphone requirements for participants in this study?	* 18 years or older * English-speaking * Able and willing to provide informed consent * Scheduled for lumbar or cervical fusion surgery at least 2 weeks from the date of enrollment * Owns a smartphone with reliable internet and/or data access * Willing to engage with SpinePal and physiological monitoring via wrist-worn...	329	3bc5e5827d9aba100b525bc964cf7f0640ca29a41332c7aae004a27705491bf2	success
95	NCT07720947	title	1	NCT07720947_1	trial_topic_question	What is the focus of this clinical trial?	Smartphone-based Nature Noticing Intervention Smartphone-based Nature Noticing Intervention for Cultivating Social Connectedness	128	45f00be33640bec5400d4b6069af9463a60edab13c6f5f15850f0a40ba66f013	success
96	NCT07720947	summary	2	NCT07720947_2	clinical_population_question	Who is the target population for this nature-noticing intervention?	We used a mixed-methods approach involving a RCT study followed by focus group discussions to obtain a more integrative understanding of the effects of a 10-week nature-noticing intervention.	191	21b9e65d813350bfa620296b80b8e707f724ae9d8af8fa688e26eb25565ad696	success
97	NCT07720947	inclusion_criteria	3	NCT07720947_3	patient_profile_question	What is the age range of the participants in this clinical trial?	* Hong Kong secondary school students * 15-17 years	53	ee4be68676cb2ea77fc7c67eb1b4afb39b6aa9789328748dc4cae8671050f006	success
98	NCT07720947	inclusion_criteria	3	NCT07720947_3	eligibility_constraint_question	Are Hong Kong secondary school students eligible to participate in this study?	* Hong Kong secondary school students * 15-17 years	53	ee4be68676cb2ea77fc7c67eb1b4afb39b6aa9789328748dc4cae8671050f006	success
99	NCT07654205	title	1	NCT07654205_1	trial_topic_question	What is the focus of this clinical trial?	Smartphone-based Intervention for Young Adults With ADHD Training Inhibitory Control Using Personalized Strategies (TIPS): A Randomized Controlled Feasibility Trial of a Smartphone-Based Intervention for Alcohol Use in Young Adults With ADHD	241	963a61943b5836f9ef60d4d9eee82c6c164d7ce9307baba7aa8ab7e827942aa1	success

End of preview. Expand in Data Studio

Dataset details:-

This is the iteration 2 of the previous dataset on same repository.
Overall similar usecase:-(i)embedding model fine-tune/training for CT(clinical trials) domain, thereby aiding downstream tsak like ranked retrieval document generation comparing 2 or more anchors, anchor vs chunks via cosine similarity.

Key changes(from earlier version):-

Greater granulation of chunks so to have:- (i) cleaner directed retreival from fine tuned embedding model; (ii) better up model metrics particularly NDCG, MRR and precision of embedded model.
More refinement in segregation of inclusion-exclusion picking possible corner cases (in terms of written format of CTs) from CT's eligiblity module.
Decrease chunk length(with proper otlier analysis), so model fine-tune/train happens efficiently(greater batch size yeilding more genralized model, less time taken).
Each CT(unique nctId) here has 3 chunks with respective number of anchors(questions) from each:-
- Title--->1 anchor ('trial_topic_question')
- Summary----> 2 anchors ('study_objective_question', 'clinical_population_question')
- Inclusion_criteria----> 2 anchors ('patient_profile_question', 'eligibility_constraint_question')
Extra care in system prompt of LLM(used to generate synthetic anchors) so to avoid generic or stock formulations that could apply equally well to many clinical trials, thereby generating other possible natural anchors to a chunk that are more focused to the given trial(corresponding nctId), its relevant disease, intervention, population, clinical context, or eligibility information.
For chunks appearing across CT records(different nctId), a hash out of chunks(hexadecimal with utf -8 encoding) named "unique_chunk_identifier" is taken as *actual_id of chunks(not
document_id)*. optimum content-level retrieval from any anchors. For CT mapoing afterwards, we are also preserving document_id. Also priortizing (content-level retrieval> clinical trial
record retreival) helps:-
- Wider application :- anchor-to-anchor, anchor-to-chunk, chunk-to-chunk simlarity analysis.
- Better precision, NDCG, MRR metrics etc in inference (opposite to when document_id would have been used as it would have penalized the anchor-positive(indices mapping) if anchor showed correlation with same chunk in different CT(ncTid).
- The fact that unique_chunk_identifiers & document_id coexist shall aid a local anchor ai (specific to a CT nctId) of same chunk ci (present in different nctIds) to align with all instances of the chunk CI = [ ci1 , ci2 ,... ciN ]

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