{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=PROMIS+Upper+Extremity", "query": { "intervention": "PROMIS Upper Extremity" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 43, "total_pages": 5, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=PROMIS+Upper+Extremity&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-06T14:15:51.057Z", "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": "NCT06050395", "title": "The MONITOR Study: Remote Monitoring Of a Nutrition Intervention To Optimize Treatment Response", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pancreatic Cancer" ], "interventions": [ { "name": "Quality fo Life Questionnaire (FHSI)", "type": "BEHAVIORAL" }, { "name": "Vioscreen Food Frequency Questionnaire (FFQ)", "type": "BEHAVIORAL" }, { "name": "Educational Handouts", "type": "BEHAVIORAL" }, { "name": "NutritionCoaching", "type": "BEHAVIORAL" }, { "name": "Follow-Up Survey", "type": "BEHAVIORAL" }, { "name": "Functional Assessment of Anorexia/Cachexia Treatment (FAACT) Questionnaire", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes Measure- Cognitive Function (PROMIS-Cog) Questionnaire", "type": "BEHAVIORAL" } ], "intervention_types": [ "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": 40, "start_date": "2023-09-12", "completion_date": "2025-02-13", "has_results": false, "last_update_posted_date": "2026-06-26", "last_synced_at": "2026-09-06T14:15:51.057Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06050395" }, { "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": "2026-09-06T14:15:51.057Z", "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": "NCT04688554", "title": "Psychosocial, Behavioral, and Radiologic Changes Following Radiosurgery for Benign Neurologic Disease", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Obsessive-Compulsive Disorder", "Pain, Intractable", "Depression" ], "interventions": [ { "name": "fMRI and DTI", "type": "DIAGNOSTIC_TEST" }, { "name": "Behavioral questionnaires", "type": "BEHAVIORAL" }, { "name": "Disease-Specific Patient-Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Behavioral tests", "type": "BEHAVIORAL" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "BEHAVIORAL" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 18, "start_date": "2020-08-25", "completion_date": "2024-02-01", "has_results": false, "last_update_posted_date": "2024-12-06", "last_synced_at": "2026-09-06T14:15:51.057Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT04688554" }, { "nct_id": "NCT02210676", "title": "Residual Extensor Lag Approximately 1 Month After Splint or Cast Immobilization of a Mallet Finger", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Patients Present With Mallet Finger" ], "interventions": [ { "name": "PROMIS Upper Extremity", "type": "OTHER" }, { "name": "Likert Pain Scale", "type": "OTHER" }, { "name": "Mallet Finger Extensor Lag Measurement", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2014-06", "completion_date": null, "has_results": false, "last_update_posted_date": "2016-12-22", "last_synced_at": "2026-09-06T14:15:51.057Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT02210676" }, { "nct_id": "NCT03164278", "title": "Effectiveness of Web-Based Training (SERT)", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Remote Transfer Training Program" ], "interventions": [ { "name": "Independent Transfer Training", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 200, "start_date": "2017-12-04", "completion_date": "2027-12-01", "has_results": false, "last_update_posted_date": "2025-12-10", "last_synced_at": "2026-09-06T14:15:51.057Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03164278" }, { "nct_id": "NCT02843750", "title": "Study of Inspiratory Muscle Training for Patients Undergoing Esophageal Surgery", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer of Esophagus", "Cancer of the Esophagus", "Esophageal Cancer", "Esophagus Cancer", "Esophagus Neoplasm", "Neoplasms, Esophageal" ], "interventions": [ { "name": "Inspiratory Muscle Training-Rehabilitation", "type": "BEHAVIORAL" }, { "name": "Questionnaires", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "40 Years to 99 Years" }, "enrollment_count": 0, "start_date": "2016-06", "completion_date": "2017-06", "has_results": false, "last_update_posted_date": "2016-12-15", "last_synced_at": "2026-09-06T14:15:51.057Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT02843750" }, { "nct_id": "NCT05524610", "title": "Development and Evaluation of a Screening Approach for Sexual Dysfunction in AYA Patients With and Surviving Childhood Cancer", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pediatric Cancer", "Survivorship" ], "interventions": [ { "name": "Sexual Function Screening Approach", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "15 Years", "maximum_age": "24 Years", "sex": "ALL", "summary": "15 Years to 24 Years" }, "enrollment_count": 205, "start_date": "2023-02-14", "completion_date": "2027-06-30", "has_results": false, "last_update_posted_date": "2026-05-06", "last_synced_at": "2026-09-06T14:15:51.057Z", "location_count": 2, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" }, { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT05524610" }, { "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": "2026-09-06T14:15:51.057Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04983641" }, { "nct_id": "NCT05726279", "title": "PROtecting Maternal Brains From Injury and Stroke", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Preeclampsia", "Maternal Hypertension" ], "interventions": [ { "name": "NIRS based personalized blood pressure management", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "55 Years", "sex": "FEMALE", "summary": "18 Years to 55 Years · Female only" }, "enrollment_count": 26, "start_date": "2023-05-04", "completion_date": "2025-02-28", "has_results": true, "last_update_posted_date": "2026-03-18", "last_synced_at": "2026-09-06T14:15:51.057Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05726279" }, { "nct_id": "NCT02658708", "title": "Bright Light on Fatigue in Women Being Treated for Breast Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Breast Neoplasms", "Breast Cancer", "Cancer of Breast", "Cancer of the Breast" ], "interventions": [ { "name": "Bright blue-green light using light visor cap", "type": "OTHER" }, { "name": "Dim red light using light visor cap", "type": "OTHER" }, { "name": "European Organization for Research and Treatment of Cancer-Quality of Life Questionnaire", "type": "OTHER" }, { "name": "Epworth Sleepiness Scale", "type": "OTHER" }, { "name": "Pittsburgh Sleep Quality Index", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Sleep Disturbance", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Cancer-Fatigue", "type": "OTHER" }, { "name": "Digital foot candle datalogging light meter (Extech Instrument, Model SDL400)", "type": "DIAGNOSTIC_TEST" }, { "name": "Polysomnography (Easy Ambulatory 2 Cadwell, Kennewick, WA)", "type": "DIAGNOSTIC_TEST" }, { "name": "Horne-Ostberg Morningness-Eveningness Questionnaire", "type": "OTHER" }, { "name": "Daily Fatigue and Sleep Log", "type": "OTHER" } ], "intervention_types": [ "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "FEMALE", "summary": "21 Years and older · Female only" }, "enrollment_count": 19, "start_date": "2015-10-12", "completion_date": "2017-05-09", "has_results": false, "last_update_posted_date": "2017-09-25", "last_synced_at": "2026-09-06T14:15:51.057Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT02658708" } ] }