{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Recovery+Group+Project&page=2", "query": { "intervention": "Recovery Group Project", "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=Recovery+Group+Project&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-05T03:01:12.979Z", "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": "NCT03578536", "title": "Effect of Constraint-Induced Gaming Therapy in an Acute Care Setting", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke" ], "interventions": [ { "name": "Recovery Rapids", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "88 Years", "sex": "ALL", "summary": "18 Years to 88 Years" }, "enrollment_count": 3, "start_date": "2019-09-30", "completion_date": "2021-06-30", "has_results": true, "last_update_posted_date": "2024-01-16", "last_synced_at": "2026-09-05T03:01:12.979Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT03578536" }, { "nct_id": "NCT00522613", "title": "Recovery Group Pilot", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bipolar Disorder", "Schizophrenia", "Schizoaffective Disorder" ], "interventions": [ { "name": "Recovery Group Project", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Kaiser Permanente", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 50, "start_date": "2005-07", "completion_date": "2006-12", "has_results": false, "last_update_posted_date": "2009-02-04", "last_synced_at": "2026-09-05T03:01:12.979Z", "location_count": 1, "location_summary": "Portland, Oregon", "locations": [ { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT00522613" }, { "nct_id": "NCT05456360", "title": "Implementation of Digital Vital Sign Monitoring to Decrease Sleep Interruption and Enhance Recovery in Phase II of the PROmoting Sleep, Patient Engagement and Recovery (PROSPER) Project", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Sleep" ], "interventions": [ { "name": "ViSi Mobile device", "type": "DEVICE" }, { "name": "Sleep enhancement intervention", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "DRUG" ], "sponsor": "M.D. Anderson 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": 89, "start_date": "2023-03-01", "completion_date": "2023-10-30", "has_results": true, "last_update_posted_date": "2024-12-18", "last_synced_at": "2026-09-05T03:01:12.979Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05456360" }, { "nct_id": "NCT07498166", "title": "Project Tendura: The Impact of Blood Flow Restriction Resistance Training (BFR-RT) in Patients With Achilles Tendon Rupture (ATR) Repair", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Achilles Tendon Rupture", "Blood Flow Restriction Therapy", "Achilles Tendon Repairs/Reconstructions", "Dynamic Blood Flow Restriction" ], "interventions": [ { "name": "Blood Flow Restriction Resistance Training (BFR-RT)", "type": "DEVICE" }, { "name": "Sham Blood Flow Restriction", "type": "DEVICE" }, { "name": "Standard Physical Therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "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": 75, "start_date": "2026-02-01", "completion_date": "2027-02-01", "has_results": false, "last_update_posted_date": "2026-04-01", "last_synced_at": "2026-09-05T03:01:12.979Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07498166" }, { "nct_id": "NCT05287711", "title": "Adjunctive Motivational Alcohol Intervention to Prevent IPV", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alcohol Use and Intimate Partner Violence" ], "interventions": [ { "name": "Motivational Enhancement Therapy", "type": "BEHAVIORAL" }, { "name": "Alcohol Education Control", "type": "BEHAVIORAL" }, { "name": "Treatment as Usual", "type": "BEHAVIORAL" }, { "name": "Strength at Home", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 300, "start_date": "2023-09-01", "completion_date": "2028-09-30", "has_results": false, "last_update_posted_date": "2025-11-20", "last_synced_at": "2026-09-05T03:01:12.979Z", "location_count": 3, "location_summary": "Boston, Massachusetts • Ann Arbor, Michigan • Minneapolis, Minnesota", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "Ann Arbor", "state": "Michigan" }, { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT05287711" }, { "nct_id": "NCT03300258", "title": "Robotic Pedaling Therapy for Targeted Neural Plasticity", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke" ], "interventions": [ { "name": "Robotic therapy", "type": "DEVICE" }, { "name": "Aerobic therapy", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Wisconsin, Madison", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 44, "start_date": "2019-06-01", "completion_date": "2022-06-29", "has_results": true, "last_update_posted_date": "2023-10-05", "last_synced_at": "2026-09-05T03:01:12.979Z", "location_count": 1, "location_summary": "Madison, Wisconsin", "locations": [ { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT03300258" }, { "nct_id": "NCT00131534", "title": "The Trauma Recovery and Resiliency Research Project", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Posttraumatic Stress Disorders" ], "interventions": [ { "name": "Individual therapy", "type": "BEHAVIORAL" }, { "name": "Group therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Cambridge Health Alliance", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 969, "start_date": "1991-08", "completion_date": "2012-01", "has_results": false, "last_update_posted_date": "2017-04-18", "last_synced_at": "2026-09-05T03:01:12.979Z", "location_count": 1, "location_summary": "Somerville, Massachusetts", "locations": [ { "city": "Somerville", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00131534" }, { "nct_id": "NCT06380179", "title": "Photomedicine Project 14: PBMT for Performance Enhancement in SOF", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Photobiomodulation Therapy", "Photomedicine", "Low-Level Laser Therapy", "Performance Enhancement", "Quadriceps", "Special Operations Readiness" ], "interventions": [ { "name": "THOR3 training + Photobiomodulation Therapy (PBMT)", "type": "DEVICE" }, { "name": "THOR3 training + sham PBMT", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Musculoskeletal Injury Rehabilitation Research for Operational Readiness", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "MALE", "summary": "18 Years to 45 Years · Male only" }, "enrollment_count": 29, "start_date": "2025-01-23", "completion_date": "2026-03-02", "has_results": true, "last_update_posted_date": "2026-06-15", "last_synced_at": "2026-09-05T03:01:12.979Z", "location_count": 1, "location_summary": "Joint Base Lewis McChord, Washington", "locations": [ { "city": "Joint Base Lewis McChord", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT06380179" }, { "nct_id": "NCT07661823", "title": "QAIAx (AIhealth4U) - AI Smart Health Cities: Microcity Enclave Program (Quantum AI/AGI Agency a/k/a AI City Hall Project - UPSTO App Nos. 64/074,526, 64/063,557, 64/105,164, 63/903,181, 63/729,428, 64/125,360)", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Asperger's Disorder", "Asperger Disorder", "Autism Disorder", "Autism", "ADHD - Attention Deficit Disorder With Hyperactivity", "ADHD", "ASD", "Alcohol Abuse/Dependence", "Alcohol Addiction", "Alcohol and Other Drug Use Disorders", "Alcohol and Other Substance Use Prevention", "Gambling Addiction", "Gambling Disorder", "Sex Abuse", "Sex Behavior", "Sex Crimes", "Sex Disorder", "Sex Disorders", "Gender Dysphoria, Adult", "Eating Behavior Disorders", "Narcotic-Related Disorders", "Narcotic Addiction", "Narcissism", "Psychiatric Disorder", "Psychedelic Effects in Healthy Volunteers", "Psychedelic Experiences", "Psychedelic Drug Dependence", "Marijuana Use Disorder", "Marijuana Abuse and Dependence", "Smoking (Tobacco) Addiction", "Smoking Among Youth", "Smoking Abstinence", "Abstinence, Sex", "Opiate Substitution Treatment", "Opioid Abuse (Disorder)", "Opioid Abuse and Addiction", "Cocaine Abuse", "MDMA ('Ecstasy')", "Addiction Disorders", "Homeless and Low Incomes People, Refugees", "Homelessness", "Reliability and Validity", "Anger Problems", "Child Abuse, Sexual" ], "interventions": [ { "name": "AI City Hall Project (AIhealth4u - Public Health Central)", "type": "BEHAVIORAL" }, { "name": "AI City Hall Project (QAIAx Microcity A - AI Public Health Central)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Veterans Recovery Network Inc.", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "17 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "17 Years to 99 Years" }, "enrollment_count": 1000000, "start_date": "2026-09-01", "completion_date": "2045-12-31", "has_results": false, "last_update_posted_date": "2026-09-04", "last_synced_at": "2026-09-05T03:01:12.979Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07661823" }, { "nct_id": "NCT01652768", "title": "PRESENCE Project: An Early Palliative Care Intervention in Brain Tumors", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Malignant Brain Tumors" ], "interventions": [ { "name": "Research Questionnaires", "type": "OTHER" }, { "name": "Palliative Care Team", "type": "OTHER" }, { "name": "Educational Information Session for Patients and Caregivers", "type": "OTHER" }, { "name": "Contact every 2 weeks", "type": "OTHER" }, { "name": "Follow-up Surgical Visit Session", "type": "OTHER" }, { "name": "Medical and/or Radiation Oncology Appointment Session", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Case Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1, "start_date": "2011-12", "completion_date": "2013-08", "has_results": false, "last_update_posted_date": "2013-08-29", "last_synced_at": "2026-09-05T03:01:12.979Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01652768" } ] }