{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=PROMIS+depression&page=2", "query": { "intervention": "PROMIS depression", "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=PROMIS+depression&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-25T22:36:08.567Z", "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": "NCT04983641", "title": "Pre-visit Digital Messaging Improves Patient Reported Outcome Measure Participation Prior to the Orthopedic Ambulatory Visit", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Orthopedic Disorder" ], "interventions": [ { "name": "Pre-Visit Messages", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Henry Ford Health System", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 291, "start_date": "2020-08-01", "completion_date": "2020-12-07", "has_results": false, "last_update_posted_date": "2021-07-30", "last_synced_at": "2026-09-25T22:36:08.567Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04983641" }, { "nct_id": "NCT06404086", "title": "RECOVER-SLEEP: Platform Protocol", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Long COVID", "Long COVID-19", "Hypersomnia", "Sleep Disturbance" ], "interventions": [ { "name": "Modafinil", "type": "DRUG" }, { "name": "Modafinil Placebo", "type": "DRUG" }, { "name": "Solriamfetol", "type": "DRUG" }, { "name": "Solriamfetol Placebo", "type": "DRUG" }, { "name": "Melatonin", "type": "DRUG" }, { "name": "Melantonin Placebo", "type": "DRUG" }, { "name": "Tailored lighting (TL) Active", "type": "DEVICE" }, { "name": "Tailored lighting (TL) Placebo", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "DEVICE" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 830, "start_date": "2024-07-31", "completion_date": "2025-12-31", "has_results": false, "last_update_posted_date": "2026-01-22", "last_synced_at": "2026-09-25T22:36:08.567Z", "location_count": 47, "location_summary": "Phoenix, Arizona • Tucson, Arizona • Palo Alto, California + 31 more", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Palo Alto", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06404086" }, { "nct_id": "NCT05122728", "title": "Post-Concussion Musculoskeletal Injury Risks", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Musculoskeletal Injury" ], "interventions": [ { "name": "Post-Concussion Neuromuscular Function and Musculoskeletal Injury Risk Assessment", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Walter Reed National Military Medical Center", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "ALL", "summary": "18 Years to 40 Years" }, "enrollment_count": 148, "start_date": "2022-10-20", "completion_date": "2027-09-30", "has_results": false, "last_update_posted_date": "2026-01-27", "last_synced_at": "2026-09-25T22:36:08.567Z", "location_count": 3, "location_summary": "Athens, Georgia • Bethesda, Maryland • Fort Bragg, North Carolina", "locations": [ { "city": "Athens", "state": "Georgia" }, { "city": "Bethesda", "state": "Maryland" }, { "city": "Fort Bragg", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05122728" }, { "nct_id": "NCT04319237", "title": "Axicabtagene Ciloleucel:Neurocognitive and Patient-Reported Outcomes", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Diffuse Large B Cell Lymphoma", "Transformed Lymphoma" ], "interventions": [ { "name": "Handgrip strength test", "type": "OTHER" }, { "name": "Neuropsychological Assessment - Wechsler Test of Adult Reading (WTAR)", "type": "BEHAVIORAL" }, { "name": "Neuropsychological Assessment - Repeatable Battery for the Assessment of Status (RBANS)", "type": "BEHAVIORAL" }, { "name": "Neuropsychological Assessment - Color Trails", "type": "BEHAVIORAL" }, { "name": "Neuropsychological Assessment -Stroop Color and Word Test", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes Measurement Information System-29 (PROMIS-29) Questionnaire", "type": "BEHAVIORAL" }, { "name": "European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire", "type": "BEHAVIORAL" }, { "name": "Quality of Life (EQ-5D-5L) Questionnaire", "type": "BEHAVIORAL" }, { "name": "PROMIS Cognitive Function 4a Questionnaire", "type": "BEHAVIORAL" }, { "name": "Comprehensive Score for Financial Toxicity (COST) measure", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "H. Lee Moffitt Cancer Center and Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2020-03-10", "completion_date": "2023-07-31", "has_results": false, "last_update_posted_date": "2026-03-02", "last_synced_at": "2026-09-25T22:36:08.567Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04319237" }, { "nct_id": "NCT03481127", "title": "Psychological Services Integration in Gynecological Oncology Clinics", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Gynecologic Oncology Patient" ], "interventions": [ { "name": "Integrated psychological care", "type": "BEHAVIORAL" }, { "name": "Surveys", "type": "OTHER" }, { "name": "Blood draw", "type": "PROCEDURE" }, { "name": "Fresh tissue from ovary", "type": "PROCEDURE" } ], "intervention_types": [ "BEHAVIORAL", "OTHER", "PROCEDURE" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 101, "start_date": "2018-05-08", "completion_date": "2019-03-26", "has_results": false, "last_update_posted_date": "2019-06-03", "last_synced_at": "2026-09-25T22:36:08.567Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT03481127" }, { "nct_id": "NCT03304587", "title": "Effects of Bright Light on Co-occurring Cancer-related Symptoms in Breast Cancer Survivors", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Polysomnography (PSG)", "type": "DIAGNOSTIC_TEST" }, { "name": "Rectal thermistor 400 Series", "type": "DIAGNOSTIC_TEST" }, { "name": "Bright blue-green light", "type": "OTHER" }, { "name": "Dim red light", "type": "OTHER" }, { "name": "Digital foot candle datalogging light meter", "type": "DIAGNOSTIC_TEST" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Cancer-Fatigue", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Sleep Disturbance", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Depression", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Physical Function", "type": "OTHER" }, { "name": "Pittsburgh Sleep Quality Index (PSQI)", "type": "OTHER" }, { "name": "Center for Epidemiological Studies - Depression", "type": "OTHER" }, { "name": "Montreal Cognitive Assessment (MoCA)", "type": "OTHER" }, { "name": "European Organization for Research and Treatment of Cancer-Quality of Life Questionnaire (EORTC QLQ-C30)", "type": "OTHER" }, { "name": "Daily Log", "type": "OTHER" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "OTHER" ], "sponsor": "Michigan State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "FEMALE", "summary": "21 Years and older · Female only" }, "enrollment_count": 30, "start_date": "2017-11-06", "completion_date": "2022-08-31", "has_results": true, "last_update_posted_date": "2025-06-10", "last_synced_at": "2026-09-25T22:36:08.567Z", "location_count": 1, "location_summary": "East Lansing, Michigan", "locations": [ { "city": "East Lansing", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT03304587" }, { "nct_id": "NCT02591472", "title": "An Integrated-Delivery-of-Care Approach to Improve Patient Outcomes, Safety, Well-Being After Orthopaedic Trauma", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Musculoskeletal Injury Trauma" ], "interventions": [ { "name": "Integrated care (ICare)", "type": "PROCEDURE" }, { "name": "Usual Care (UsCare)", "type": "PROCEDURE" }, { "name": "Patient-Reported Outcomes Measurement Information System", "type": "OTHER" }, { "name": "Lower Extremity Gain Scale (LEGS)", "type": "OTHER" }, { "name": "Dynamometer", "type": "OTHER" }, { "name": "Active Range of Motion (AROM)", "type": "OTHER" }, { "name": "Posttraumatic Stress Disorder (PTSD)", "type": "OTHER" }, { "name": "Beck Depression Inventory-II", "type": "OTHER" }, { "name": "State-Trait Anxiety Inventory (STAI)", "type": "OTHER" }, { "name": "Tampa Scale of Kinesiophobia-11 (TSK-11)", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 88, "start_date": "2016-01-11", "completion_date": "2023-01-01", "has_results": true, "last_update_posted_date": "2024-10-28", "last_synced_at": "2026-09-25T22:36:08.567Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02591472" }, { "nct_id": "NCT03823651", "title": "A Research Program Targeting Pre- and Peri-transplant Optimization Program (R-PPOP)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hematologic Malignancy" ], "interventions": [ { "name": "Interval training", "type": "BEHAVIORAL" }, { "name": "Psychiatric consult", "type": "BEHAVIORAL" }, { "name": "Nutrition/diet evaluation", "type": "BEHAVIORAL" }, { "name": "Referral to Social Worker", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 29, "start_date": "2019-05-06", "completion_date": "2024-04-27", "has_results": true, "last_update_posted_date": "2024-09-27", "last_synced_at": "2026-09-25T22:36:08.567Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03823651" }, { "nct_id": "NCT05859386", "title": "Optimizing Mindfulness Based Cognitive Therapy (MBCT) Maintenance", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression" ], "interventions": [ { "name": "Mindfulness maintenance program", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 34, "start_date": "2023-04-03", "completion_date": "2024-02-19", "has_results": false, "last_update_posted_date": "2024-07-03", "last_synced_at": "2026-09-25T22:36:08.567Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05859386" }, { "nct_id": "NCT05111925", "title": "Pre- and Post-neuromusculoskeletal Injury Risk Evaluation for Return-to-Duty Enhancement", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Musculoskeletal Injuries" ], "interventions": [ { "name": "PREPARE Initial Clinical Assessment - Pilot (two iterations)", "type": "OTHER" }, { "name": "PREPARE Initial Clinical Assessment - Pre-Injury (one iteration)", "type": "OTHER" }, { "name": "PREPARE Initial Clinical Assessment - Post-Injury (up to three iterations)", "type": "OTHER" }, { "name": "PREPARE Optimized Clinical Assessment", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Womack Army Medical Center", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "44 Years", "sex": "ALL", "summary": "18 Years to 44 Years" }, "enrollment_count": 2690, "start_date": "2022-10-26", "completion_date": "2028-05-31", "has_results": false, "last_update_posted_date": "2026-06-03", "last_synced_at": "2026-09-25T22:36:08.567Z", "location_count": 2, "location_summary": "Bethesda, Maryland • Fort Liberty, North Carolina", "locations": [ { "city": "Bethesda", "state": "Maryland" }, { "city": "Fort Liberty", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05111925" } ] }