{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Study+Diary&page=2", "query": { "intervention": "Study Diary", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Study+Diary&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-11T12:53:00.883Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT02489422", "title": "Programs To Support You During Chemotherapy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression", "Fatigue", "Stage IIA Colorectal Cancer", "Stage IIB Colorectal Cancer", "Stage IIC Colorectal Cancer", "Stage IIIA Colorectal Cancer", "Stage IIIB Colorectal Cancer", "Stage IIIC Colorectal Cancer", "Stage IVA Colorectal Cancer", "Stage IVB Colorectal Cancer", "Pancreatic Cancer", "Esophageal Cancer", "Appendix Cancer", "Stomach Cancer", "Gallbladder Cancer", "Liver Cancer", "Small Intestine Cancer", "Large Intestine Cancer", "Anal Cancer", "Biliary Tract Cancer", "Gastrointestinal Stromal Cancer" ], "interventions": [ { "name": "Laboratory Biomarker Analysis", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Daily Survey Administration", "type": "OTHER" }, { "name": "Yoga Skills Training", "type": "BEHAVIORAL" }, { "name": "Attention Control", "type": "BEHAVIORAL" }, { "name": "Actigraphy Assessment", "type": "OTHER" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 44, "start_date": "2016-08", "completion_date": "2020-01", "has_results": true, "last_update_posted_date": "2022-10-14", "last_synced_at": "2026-09-11T12:53:00.883Z", "location_count": 2, "location_summary": "Winston-Salem, North Carolina • Nashville, Tennessee", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" }, { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02489422" }, { "nct_id": "NCT04855773", "title": "Comparing Mobile Health Strategies to Improve Pre-exposure Prophylaxis Use (PrEP) for HIV Prevention", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Infections", "Sexually Transmitted Diseases" ], "interventions": [ { "name": "PrEPmate", "type": "OTHER" }, { "name": "Dot Diary", "type": "DEVICE" } ], "intervention_types": [ "OTHER", "DEVICE" ], "sponsor": "Public Health Foundation Enterprises, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "15 Years", "maximum_age": null, "sex": "ALL", "summary": "15 Years and older" }, "enrollment_count": 300, "start_date": "2021-07-21", "completion_date": "2023-08", "has_results": false, "last_update_posted_date": "2022-09-28", "last_synced_at": "2026-09-11T12:53:00.883Z", "location_count": 4, "location_summary": "San Francisco, California • Washington D.C., District of Columbia • Miami, Florida", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04855773" }, { "nct_id": "NCT07316153", "title": "Deep Sleep in Older Adults", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Insomnia", "Insomnia Chronic" ], "interventions": [ { "name": "CBT-I-IoT-AI", "type": "BEHAVIORAL" }, { "name": "SleepEZ CBTi", "type": "BEHAVIORAL" }, { "name": "Sleep Hygiene IoT", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Proactive Life Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 180, "start_date": "2026-03-01", "completion_date": "2026-12-30", "has_results": false, "last_update_posted_date": "2026-01-05", "last_synced_at": "2026-09-11T12:53:00.883Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07316153" }, { "nct_id": "NCT03421145", "title": "A Clinical Study to Evaluate Effects of an Oral Rinse on Plaque and Gingivitis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [], "conditions": [ "Plaque" ], "interventions": [ { "name": "3M™ Oral Rinse", "type": "DEVICE" }, { "name": "Vehicle Control Oral Rinse", "type": "OTHER" }, { "name": "PerioShield™ Oral Health Rinse", "type": "DEVICE" }, { "name": "Water", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Solventum US LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 200, "start_date": "2017-12-17", "completion_date": "2019-01-17", "has_results": true, "last_update_posted_date": "2024-10-01", "last_synced_at": "2026-09-11T12:53:00.883Z", "location_count": 1, "location_summary": "Loma Linda, California", "locations": [ { "city": "Loma Linda", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03421145" }, { "nct_id": "NCT00710619", "title": "Observational Patient Diary Study of Treatment Doses for Patients With Haemophilia With Inhibitors to Factors VIII and IX", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Congenital Bleeding Disorder", "Haemophilia A With Inhibitors", "Haemophilia B With Inhibitors" ], "interventions": [ { "name": "activated recombinant human factor VII", "type": "DRUG" }, { "name": "Feiba VH", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Novo Nordisk A/S", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "MALE", "summary": "Male only" }, "enrollment_count": 52, "start_date": "2008-06", "completion_date": "2009-07", "has_results": false, "last_update_posted_date": "2016-11-17", "last_synced_at": "2026-09-11T12:53:00.883Z", "location_count": 1, "location_summary": "Plainsboro, New Jersey", "locations": [ { "city": "Plainsboro", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT00710619" }, { "nct_id": "NCT07202247", "title": "Metabolic Interventions (Time-Restricted Eating, GLP1 Receptor Agonist, and Heart Healthy Diet) to Improve Cardiometabolic Health in Prostate Cancer Patients During Androgen Deprivation Therapy, IMPACT-ADT Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Prostate Carcinoma", "Recurrent Prostate Carcinoma" ], "interventions": [ { "name": "Antiandrogen Therapy", "type": "DRUG" }, { "name": "Behavioral Intervention", "type": "BEHAVIORAL" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Cardiac Computerized Tomographic Angiography", "type": "PROCEDURE" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Electronic Health Record Review", "type": "OTHER" }, { "name": "Internet-Based Intervention", "type": "OTHER" }, { "name": "Lifestyle Counseling", "type": "BEHAVIORAL" }, { "name": "Medical Device Usage and Evaluation", "type": "OTHER" }, { "name": "Nutritional Intervention", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Radiation Therapy", "type": "RADIATION" }, { "name": "Referral", "type": "OTHER" }, { "name": "Semaglutide", "type": "DRUG" }, { "name": "Short-Term Fasting", "type": "OTHER" }, { "name": "Tirzepatide", "type": "DRUG" } ], "intervention_types": [ "DRUG", "BEHAVIORAL", "PROCEDURE", "OTHER", "RADIATION" ], "sponsor": "City of Hope Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": "79 Years", "sex": "MALE", "summary": "30 Years to 79 Years · Male only" }, "enrollment_count": 60, "start_date": "2025-11-05", "completion_date": "2028-04-09", "has_results": false, "last_update_posted_date": "2026-08-17", "last_synced_at": "2026-09-11T12:53:00.883Z", "location_count": 1, "location_summary": "Duarte, California", "locations": [ { "city": "Duarte", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07202247" }, { "nct_id": "NCT05536050", "title": "Study of Low-dose Naltrexone in Chronic Migraine With Fibromyalgia", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Chronic Migraine", "Fibromyalgia", "New Daily Persistent Headache" ], "interventions": [ { "name": "Migraine diary and Questionnaires", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Thomas Jefferson University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 30, "start_date": "2022-07-28", "completion_date": "2023-12", "has_results": false, "last_update_posted_date": "2022-10-27", "last_synced_at": "2026-09-11T12:53:00.883Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05536050" }, { "nct_id": "NCT07720323", "title": "Evaluating Whether a Nausea Band Reduces Symptoms in Those With Chronic Nausea Vomiting", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Nausea", "Chronic Nausea and Vomiting Syndrome" ], "interventions": [ { "name": "EmeTerm wearable TENS device", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2023-02-01", "completion_date": "2028-06-30", "has_results": false, "last_update_posted_date": "2026-07-22", "last_synced_at": "2026-09-11T12:53:00.883Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT07720323" }, { "nct_id": "NCT02990988", "title": "Microbiome of Donor Iron Deficient Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Iron Deficiency" ], "interventions": [], "intervention_types": [], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 70, "start_date": "2017-01", "completion_date": "2022-06-03", "has_results": false, "last_update_posted_date": "2022-09-19", "last_synced_at": "2026-09-11T12:53:00.883Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02990988" }, { "nct_id": "NCT01738152", "title": "Non-Hormonal Vaginal Moisturizer in Hormone-Receptor Positive Postmenopausal Cancer Survivors Experiencing Estrogen Deprivation Symptoms on Vulvovaginal Health", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer", "Endometrial Cancer" ], "interventions": [ { "name": "HLA vaginal gel (HyaloGYN®),", "type": "OTHER" }, { "name": "questionnaires", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 106, "start_date": "2012-11", "completion_date": "2021-07-21", "has_results": false, "last_update_posted_date": "2021-07-23", "last_synced_at": "2026-09-11T12:53:00.883Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01738152" } ] }