{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Symptom+Questionnaire+Measures&page=2", "query": { "intervention": "Symptom Questionnaire Measures", "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=Symptom+Questionnaire+Measures&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-26T14:37:08.742Z", "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": "NCT02083744", "title": "Project Fluido: Fluid Watchers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Congestive Heart Failure" ], "interventions": [ { "name": "PsychoEducational Support", "type": "BEHAVIORAL" }, { "name": "Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 42, "start_date": "2013-06", "completion_date": "2014-12-22", "has_results": false, "last_update_posted_date": "2020-02-17", "last_synced_at": "2026-09-26T14:37:08.742Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02083744" }, { "nct_id": "NCT05913505", "title": "Heart Rate Variability Biofeedback Following Traumatic Brain Injury", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Traumatic Brain Injury" ], "interventions": [ { "name": "OSC-", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Brigham Young University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "18 Years to 55 Years" }, "enrollment_count": 50, "start_date": "2023-02-15", "completion_date": "2024-04-24", "has_results": false, "last_update_posted_date": "2023-06-22", "last_synced_at": "2026-09-26T14:37:08.742Z", "location_count": 1, "location_summary": "Provo, Utah", "locations": [ { "city": "Provo", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT05913505" }, { "nct_id": "NCT01144741", "title": "Survey Study and Records Review of Treatment Outcomes in Freeman-Sheldon Syndrome", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Freeman-Sheldon Syndrome", "Arthrogryposis Distal Type 2A", "Whistling Face Syndrome", "Craniocarpotarsal Dysplasia", "Craniocarpotarsal Dystrophy", "Freeman-Sheldon Syndrome Variant", "Sheldon-Hall Syndrome", "Arthrogryposis Distal Type 2B", "Gordon Syndrome", "Arthrogryposis Distal Type 3", "Arthrogryposis Distal Type 1", "Arthrogryposis, Distal, Type 1A", "Arthrogryposis Distal Type 1B", "Arthrogryposis, Distal", "Craniofacial Abnormalities", "Arthrogryposis" ], "interventions": [ { "name": "PTSD Checklist-Civilian (PCL-C)", "type": "OTHER" }, { "name": "Modified Flanagan Quality of Life Scale", "type": "OTHER" }, { "name": "Center for Epidemiologic Studies Depression Scale (CES-D)", "type": "OTHER" }, { "name": "Functional Enquiry (or Review of Systems) Form", "type": "OTHER" }, { "name": "Study of Therapeutic Outcomes and Practices in Freeman-Sheldon Syndrome (STOP-FSS) Questionnaire", "type": "OTHER" }, { "name": "FSRG Semi-Structured Quality of Life Interview (FSRG SSQLI)", "type": "OTHER" }, { "name": "Medical Records Review", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Freeman-Sheldon Research Group, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 2, "start_date": "2010-02", "completion_date": "2022-06-14", "has_results": false, "last_update_posted_date": "2022-06-21", "last_synced_at": "2026-09-26T14:37:08.742Z", "location_count": 1, "location_summary": "Buckhannon, West Virginia", "locations": [ { "city": "Buckhannon", "state": "West Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01144741" }, { "nct_id": "NCT05227599", "title": "BRAVE: Building Resilience and Values Through E-health", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Survivorship" ], "interventions": [ { "name": "Online survey questionnaire", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "11 Years", "maximum_age": "25 Years", "sex": "ALL", "summary": "11 Years to 25 Years" }, "enrollment_count": 56, "start_date": "2021-03-01", "completion_date": "2022-03-24", "has_results": false, "last_update_posted_date": "2023-09-13", "last_synced_at": "2026-09-26T14:37:08.742Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05227599" }, { "nct_id": "NCT01495780", "title": "eRT Remote Health Monitoring", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pulmonary Disease, Chronic Obstructive", "COPD", "Chronic Obstructive Lung Disease", "Bronchitis, Chronic", "Pulmonary Emphysema" ], "interventions": [ { "name": "Remote Health Monitoring", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 17, "start_date": "2012-01", "completion_date": "2014-08-20", "has_results": false, "last_update_posted_date": "2020-05-01", "last_synced_at": "2026-09-26T14:37:08.742Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01495780" }, { "nct_id": "NCT00836238", "title": "Questionnaire and Fall Risk Assessment", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Prostate Cancer" ], "interventions": [ { "name": "Interview", "type": "BEHAVIORAL" }, { "name": "Physical Function Tests", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "MALE", "summary": "65 Years and older · Male only" }, "enrollment_count": 34, "start_date": "2009-02", "completion_date": "2009-06", "has_results": false, "last_update_posted_date": "2012-08-01", "last_synced_at": "2026-09-26T14:37:08.742Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00836238" }, { "nct_id": "NCT06861608", "title": "A Single-session Intervention Adaptation of the Habit Framework for the Prevention of Eating Disorders", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Eating Disorder Not Otherwise Specified" ], "interventions": [ { "name": "Screening Questionnaire", "type": "BEHAVIORAL" }, { "name": "Pre-Intervention Questionnaires (~10 minutes)", "type": "BEHAVIORAL" }, { "name": "SSI (Single-session intervention (~30 minutes) Active arm", "type": "BEHAVIORAL" }, { "name": "SSI (Single-session intervention (~30 minutes) control arm", "type": "BEHAVIORAL" }, { "name": "End-of-Intervention Questionnaires (~5 minutes)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Virginia Commonwealth University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "22 Years", "sex": "ALL", "summary": "18 Years to 22 Years" }, "enrollment_count": 160, "start_date": "2025-01-15", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-08-05", "last_synced_at": "2026-09-26T14:37:08.742Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06861608" }, { "nct_id": "NCT04002531", "title": "A One Visit Follow Up of Adults With Fabry Disease Who Started Long-term Enzyme Replacement Therapy As Children", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Quality of Life", "Renal Insufficiency", "Cardiac Event" ], "interventions": [ { "name": "General and Neurological examination", "type": "OTHER" }, { "name": "Vital signs", "type": "OTHER" }, { "name": "12 lead electrocardiogram", "type": "PROCEDURE" }, { "name": "Echocardiogram", "type": "PROCEDURE" }, { "name": "Blood draw", "type": "PROCEDURE" }, { "name": "Urine collection", "type": "PROCEDURE" }, { "name": "2-hour Holter Monitor", "type": "PROCEDURE" }, { "name": "Brief Pain Inventory questionnaire", "type": "OTHER" }, { "name": "Quality of Life questionnaire", "type": "OTHER" } ], "intervention_types": [ "OTHER", "PROCEDURE" ], "sponsor": "Baylor 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": 5, "start_date": "2018-11-10", "completion_date": "2019-12-13", "has_results": false, "last_update_posted_date": "2026-03-04", "last_synced_at": "2026-09-26T14:37:08.742Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04002531" }, { "nct_id": "NCT07673237", "title": "Remote Evaluation and Surveillance of Patients With Interstitial Lung Disease: Transforming ILD Care Delivery With Remote Monitoring", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Fibrotic Interstitial Lung Disease", "IPF and PPF", "Lung Fibrosis Interstitial" ], "interventions": [ { "name": "Home Monitoring in Patients with f-ILD", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 200, "start_date": "2026-08-01", "completion_date": "2028-08-01", "has_results": false, "last_update_posted_date": "2026-06-29", "last_synced_at": "2026-09-26T14:37:08.742Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07673237" }, { "nct_id": "NCT04388735", "title": "Multiple Myeloma (MM) Quality of Life (QOL) Study", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Multiple Myeloma", "Quality of Life", "Symptom, Behavioral" ], "interventions": [ { "name": "Questionnaire", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 360, "start_date": "2020-06", "completion_date": "2022-05-16", "has_results": false, "last_update_posted_date": "2020-05-14", "last_synced_at": "2026-09-26T14:37:08.742Z", "location_count": 3, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04388735" } ] }