{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Promis+Physical+Function+Questionnaire", "query": { "intervention": "Promis Physical Function Questionnaire" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 31, "total_pages": 4, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Promis+Physical+Function+Questionnaire&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-02T18:20:22.294Z", "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": "NCT01788839", "title": "Longitudinal Sexual and Reproductive Health Study of Women With Breast Cancer and Lymphoma", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Cancer", "Lymphoma", "Hodgkin's Lymphoma" ], "interventions": [ { "name": "surveys", "type": "BEHAVIORAL" }, { "name": "Blood draw", "type": "OTHER" }, { "name": "Transvaginal ultrasounds", "type": "DEVICE" } ], "intervention_types": [ "BEHAVIORAL", "OTHER", "DEVICE" ], "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": 475, "start_date": "2013-02", "completion_date": "2027-02", "has_results": false, "last_update_posted_date": "2026-03-04", "last_synced_at": "2026-09-02T18:20:22.294Z", "location_count": 7, "location_summary": "Basking Ridge, New Jersey • Middletown, New Jersey • Montvale, New Jersey + 4 more", "locations": [ { "city": "Basking Ridge", "state": "New Jersey" }, { "city": "Middletown", "state": "New Jersey" }, { "city": "Montvale", "state": "New Jersey" }, { "city": "Commack", "state": "New York" }, { "city": "Harrison", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01788839" }, { "nct_id": "NCT02914067", "title": "Cognitive Biomarkers in Pediatric Brain Tumor Patients", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Childhood Brain Tumor" ], "interventions": [ { "name": "Neurocognitive testing", "type": "OTHER" }, { "name": "rsfcMRI", "type": "DEVICE" } ], "intervention_types": [ "OTHER", "DEVICE" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "4 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "4 Years to 18 Years" }, "enrollment_count": 200, "start_date": "2016-10-26", "completion_date": "2029-01-31", "has_results": false, "last_update_posted_date": "2025-11-21", "last_synced_at": "2026-09-02T18:20:22.294Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT02914067" }, { "nct_id": "NCT06616363", "title": "Does a Periaqueductal Gray-vagus Nerve Interface Malfunction Explain the Nat hx With Its Numerous Co-morbidities?", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "POTS - Postural Orthostatic Tachycardia Syndrome" ], "interventions": [ { "name": "Questionnaires to be competed", "type": "BEHAVIORAL" }, { "name": "Provide list of medication and lifetime events", "type": "BEHAVIORAL" }, { "name": "Use phone App to record new life events", "type": "BEHAVIORAL" }, { "name": "Will wear an activity monitor", "type": "DEVICE" }, { "name": "Periodic 24-hour urine sodium check", "type": "OTHER" }, { "name": "A fMRI scan", "type": "DIAGNOSTIC_TEST" }, { "name": "A bedside tilt test will be performed", "type": "DIAGNOSTIC_TEST" }, { "name": "IV placed to collect blood samples", "type": "OTHER" }, { "name": "Stool Sample", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE", "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "Virginia Commonwealth University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Years", "maximum_age": "21 Years", "sex": "FEMALE", "summary": "12 Years to 21 Years · Female only" }, "enrollment_count": 120, "start_date": "2024-05-29", "completion_date": "2028-07", "has_results": false, "last_update_posted_date": "2025-09-26", "last_synced_at": "2026-09-02T18:20:22.294Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06616363" }, { "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": "2026-09-02T18:20:22.294Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02591472" }, { "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": "2026-09-02T18:20:22.294Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04319237" }, { "nct_id": "NCT05926024", "title": "Long-Term Follow-Up in Women With Early Breast Cancer Three Years of More Post Primary Treatment", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Exercise Recall Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Health Behavior Questionnaire (HBQ)30 Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Functional Assessment of Cancer Therapy-General (FACT-G) Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes PROMIS Cognitive Function (Short Form 8a)", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes Functional Assessment of Cancer-Gynecology Oncology Group-Neurotoxicity (FACT/GOG-NTX-12)", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes PROMIS", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes FACT-Endocrine Symptoms", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes Penn Arthralgia Aging Survey", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes PRO-CTCAE (patient-reported CTCAE)", "type": "BEHAVIORAL" }, { "name": "p16 tumor suppressor gene", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "BEHAVIORAL", "DIAGNOSTIC_TEST" ], "sponsor": "UNC Lineberger Comprehensive Cancer Center", "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": 253, "start_date": "2023-01-06", "completion_date": "2028-01-31", "has_results": false, "last_update_posted_date": "2026-03-11", "last_synced_at": "2026-09-02T18:20:22.294Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05926024" }, { "nct_id": "NCT07723495", "title": "Symptom Management to Improve Completion of Patient-reported Outcome Measures", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Malignant Solid Neoplasm", "Malignant Head and Neck Neoplasm", "Malignant Lung Neoplasm" ], "interventions": [ { "name": "Monitoring of PROMIS symptoms and physical function", "type": "BEHAVIORAL" }, { "name": "Monitoring of additional symptoms and symptom self-management", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "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": 78, "start_date": "2027-10-01", "completion_date": "2031-09-01", "has_results": false, "last_update_posted_date": "2026-07-29", "last_synced_at": "2026-09-02T18:20:22.294Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT07723495" }, { "nct_id": "NCT07631026", "title": "Wearable Device Tracked Recovery From Autologous Breast Reconstructive Surgery", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Questionnaires", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "M.D. Anderson 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": 50, "start_date": "2026-12-31", "completion_date": "2029-12-31", "has_results": false, "last_update_posted_date": "2026-07-27", "last_synced_at": "2026-09-02T18:20:22.294Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07631026" }, { "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": "2026-09-02T18:20:22.294Z", "location_count": 1, "location_summary": "East Lansing, Michigan", "locations": [ { "city": "East Lansing", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT03304587" }, { "nct_id": "NCT03761706", "title": "Impact of Home-based Aerobic and Strength Exercises During Chemotherapy for Early Breast Cancer on Biomarkers of Aging", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Engagement in Physical Activity", "type": "BEHAVIORAL" }, { "name": "Questionnaires", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "UNC Lineberger Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "99 Years", "sex": "FEMALE", "summary": "21 Years to 99 Years · Female only" }, "enrollment_count": 132, "start_date": "2018-02-28", "completion_date": "2025-02-01", "has_results": false, "last_update_posted_date": "2025-04-01", "last_synced_at": "2026-09-02T18:20:22.294Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03761706" } ] }