{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Patient+Reported+Outcome+Measure+%28PROM%29", "query": { "intervention": "Patient Reported Outcome Measure (PROM)" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 14, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Patient+Reported+Outcome+Measure+%28PROM%29&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-13T15:08:28.949Z", "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": "NCT06078137", "title": "Impact of an Enhanced Patient Reported Outcome Measurement (PROM) Strategy on PROM Completion Rates", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "PROM" ], "interventions": [ { "name": "Usual PROMs and new PROMs strategy", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Texas at Austin", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 200, "start_date": "2023-09-01", "completion_date": "2025-12-01", "has_results": false, "last_update_posted_date": "2026-06-09", "last_synced_at": "2026-09-13T15:08:28.949Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06078137" }, { "nct_id": "NCT04595851", "title": "Pharmacists Coordinated Care Oncology Model (PCOM) for Patients Taking Oral Anti-cancer Medications", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Myeloid Leukemia", "Chronic Lymphocytic Leukemia", "Multiple Chronic Conditions" ], "interventions": [ { "name": "Patient Reported Outcome Measure (PROM)", "type": "OTHER" }, { "name": "Comprehensive Medication Review (CMR)", "type": "OTHER" }, { "name": "Communications between oncology and primary care pharmacists", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Michigan Rogel Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 6, "start_date": "2021-03-26", "completion_date": "2022-07-14", "has_results": false, "last_update_posted_date": "2022-11-22", "last_synced_at": "2026-09-13T15:08:28.949Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04595851" }, { "nct_id": "NCT05597046", "title": "Qualitative Interviews With Healthcare Professionals", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Total Knee Replacement" ], "interventions": [ { "name": "Interview", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Invibio Ltd", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 6, "start_date": "2022-11-03", "completion_date": "2022-11-05", "has_results": false, "last_update_posted_date": "2022-11-09", "last_synced_at": "2026-09-13T15:08:28.949Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05597046" }, { "nct_id": "NCT05402033", "title": "Cancer Clinical Trials Financial Reimbursement Program", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cancer Clinical Trials" ], "interventions": [ { "name": "Survey / Interview Group", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Texas Southwestern Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 1200, "start_date": "2022-07-12", "completion_date": "2030-06-01", "has_results": false, "last_update_posted_date": "2026-09-02", "last_synced_at": "2026-09-13T15:08:28.949Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05402033" }, { "nct_id": "NCT04746456", "title": "Vulvovaginal Atrophy Questionnaire (VVAQ): Psychometric Validation of a Novel PROM", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Vulvovaginal Atrophy", "Menopause", "Genitourinary Syndrome of Menopause" ], "interventions": [], "intervention_types": [], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "45 Years", "maximum_age": null, "sex": "FEMALE", "summary": "45 Years and older · Female only" }, "enrollment_count": 210, "start_date": "2022-09-01", "completion_date": "2024-05-01", "has_results": false, "last_update_posted_date": "2025-05-30", "last_synced_at": "2026-09-13T15:08:28.949Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04746456" }, { "nct_id": "NCT04852471", "title": "Improving Quality of Life Using Patient Reported Outcomes Measures Post-operative Via Text Messaging", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Gynecologic Cancer" ], "interventions": [ { "name": "Standard Post-Operative Counseling + FACT-G", "type": "BEHAVIORAL" }, { "name": "PROM symptom tracker", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan Rogel 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": 102, "start_date": "2022-01-05", "completion_date": "2023-05-02", "has_results": false, "last_update_posted_date": "2023-10-11", "last_synced_at": "2026-09-13T15:08:28.949Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04852471" }, { "nct_id": "NCT05738330", "title": "Symptom Monitoring in Hemodialysis", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "End Stage Kidney Disease" ], "interventions": [ { "name": "Symptom Monitoring on Renal Replacement Therapy - Hemodialysis (SMaRRT-HD)", "type": "BEHAVIORAL" }, { "name": "Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2400, "start_date": "2023-06-24", "completion_date": "2027-09", "has_results": false, "last_update_posted_date": "2025-11-24", "last_synced_at": "2026-09-13T15:08:28.949Z", "location_count": 1, "location_summary": "Waltham, Massachusetts", "locations": [ { "city": "Waltham", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05738330" }, { "nct_id": "NCT05388045", "title": "Piloting a Patient-Reported Outcome Measure for Opioid Use Disorder Recovery in a Clinical Setting", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Substance Use Disorders", "Opioid Use Disorder" ], "interventions": [ { "name": "Patient Reported Outcome Measure", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Brandeis University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2022-04-14", "completion_date": "2023-11-01", "has_results": false, "last_update_posted_date": "2023-07-27", "last_synced_at": "2026-09-13T15:08:28.949Z", "location_count": 1, "location_summary": "Fall River, Massachusetts", "locations": [ { "city": "Fall River", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05388045" }, { "nct_id": "NCT02749305", "title": "Comparative Effectiveness of Metabolic and Bariatric Surgery With PROMs", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bariatric Surgery", "Metabolic Surgery", "Weight Reduction" ], "interventions": [ { "name": "Collection of patient-reported outcome measures", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "0 Years", "maximum_age": null, "sex": "ALL", "summary": "0 Years and older" }, "enrollment_count": 11146, "start_date": "2016-03", "completion_date": "2024-02-01", "has_results": false, "last_update_posted_date": "2025-04-20", "last_synced_at": "2026-09-13T15:08:28.949Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT02749305" }, { "nct_id": "NCT04805554", "title": "Incorporating Patient-Reported Outcomes Into Shared Decision Making With Patients With Osteoarthritis of the Hip or Knee", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Osteo Arthritis Knee" ], "interventions": [ { "name": "Joint Insights decision aid", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Texas at Austin", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "45 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "45 Years to 89 Years" }, "enrollment_count": 200, "start_date": "2021-02-22", "completion_date": "2023-05-30", "has_results": false, "last_update_posted_date": "2024-01-05", "last_synced_at": "2026-09-13T15:08:28.949Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04805554" } ] }