{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Reduced+Activity&page=88", "query": { "intervention": "Reduced Activity", "page": 88 }, "page_size": 10 }, "pagination": { "page": 88, "page_size": 10, "total_count": 2213, "total_pages": 222, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Reduced+Activity&page=89&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Reduced+Activity&page=87&page_size=10" }, "source": "remote", "last_synced_at": "2026-11-11T08:47:25.637Z", "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": "NCT02008565", "title": "Controlling Anal Incontinence by Performing Anal Exercises With Biofeedback or Loperamide (CAPABLe)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Fecal Incontinence" ], "interventions": [ { "name": "Loperamide", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Anal exercises with biofeedback", "type": "BEHAVIORAL" }, { "name": "Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "DRUG", "BEHAVIORAL" ], "sponsor": "NICHD Pelvic Floor Disorders Network", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 300, "start_date": "2014-02", "completion_date": "2016-05", "has_results": true, "last_update_posted_date": "2018-11-20", "last_synced_at": "2026-11-11T08:47:25.637Z", "location_count": 9, "location_summary": "Birmingham, Alabama • La Jolla, California • San Diego, California + 6 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "La Jolla", "state": "California" }, { "city": "San Diego", "state": "California" }, { "city": "Albuquerque", "state": "New Mexico" }, { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT02008565" }, { "nct_id": "NCT05588778", "title": "Cognitive Enhancement and Risk-reduction Through Exercise for Brain-Related Outcomes", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Aging" ], "interventions": [ { "name": "BAILAMOS™ @home/en casa", "type": "BEHAVIORAL" }, { "name": "¡En Forma y Fuerte! @home/en casa", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Illinois Chicago", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "60 Years", "maximum_age": null, "sex": "ALL", "summary": "60 Years and older" }, "enrollment_count": 37, "start_date": "2023-08-01", "completion_date": "2024-11-01", "has_results": false, "last_update_posted_date": "2024-11-08", "last_synced_at": "2026-11-11T08:47:25.637Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05588778" }, { "nct_id": "NCT03459625", "title": "Mindfulness for Parents of Children With Autism Spectrum Disorder Autism Spectrum Disorder", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Autism Spectrum Disorder" ], "interventions": [ { "name": "Mindfulness-Based Stress Reduction (MSBR)", "type": "BEHAVIORAL" }, { "name": "Psychoeducational Support Group (PE)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Loma Linda University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "3 Years", "maximum_age": "5 Years", "sex": "ALL", "summary": "3 Years to 5 Years" }, "enrollment_count": 118, "start_date": "2018-07-21", "completion_date": "2022-06-28", "has_results": true, "last_update_posted_date": "2023-11-13", "last_synced_at": "2026-11-11T08:47:25.637Z", "location_count": 1, "location_summary": "Loma Linda, California", "locations": [ { "city": "Loma Linda", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03459625" }, { "nct_id": "NCT00106574", "title": "A Study to Assess the Effect of Tocilizumab + DMARD Therapy on Signs and Symptoms in Patients With Moderate to Severe Active Rheumatoid Arthritis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Rheumatoid Arthritis" ], "interventions": [ { "name": "Placebo", "type": "DRUG" }, { "name": "tocilizumab [RoActemra/Actemra]", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Hoffmann-La Roche", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1220, "start_date": "2005-04", "completion_date": "2007-12", "has_results": false, "last_update_posted_date": "2016-11-02", "last_synced_at": "2026-11-11T08:47:25.637Z", "location_count": 76, "location_summary": "Mesa, Arizona • Paradise Valley, Arizona • Peoria, Arizona + 71 more", "locations": [ { "city": "Mesa", "state": "Arizona" }, { "city": "Paradise Valley", "state": "Arizona" }, { "city": "Peoria", "state": "Arizona" }, { "city": "Scottsdale", "state": "Arizona" }, { "city": "Tucson", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT00106574" }, { "nct_id": "NCT03076125", "title": "Stroke COunseling for Risk REduction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke" ], "interventions": [ { "name": "SCORRE", "type": "BEHAVIORAL" }, { "name": "Attention-Control Activity", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Georgia State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "20 Years", "maximum_age": "35 Years", "sex": "ALL", "summary": "20 Years to 35 Years" }, "enrollment_count": 116, "start_date": "2017-03-01", "completion_date": "2017-12-20", "has_results": false, "last_update_posted_date": "2018-12-13", "last_synced_at": "2026-11-11T08:47:25.637Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT03076125" }, { "nct_id": "NCT03932097", "title": "REAL Parenting Alcohol and Substance Use App", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Underage Drinking", "Alcohol Use, Underage" ], "interventions": [ { "name": "REAL Parenting", "type": "BEHAVIORAL" }, { "name": "Active Control Materials", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Real Prevention, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "15 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "15 Years to 18 Years" }, "enrollment_count": 612, "start_date": "2021-01-15", "completion_date": "2022-05-31", "has_results": true, "last_update_posted_date": "2026-10-27", "last_synced_at": "2026-11-11T08:47:25.637Z", "location_count": 1, "location_summary": "Clifton, New Jersey", "locations": [ { "city": "Clifton", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT03932097" }, { "nct_id": "NCT06606574", "title": "Intrathecal Baclofen and Pediatric Dystonia", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Dystonic Cerebral Palsy" ], "interventions": [ { "name": "ITB Titration Protocol", "type": "DRUG" }, { "name": "Ventral Dorsal Rhizotomy", "type": "PROCEDURE" }, { "name": "Deep Brain Stimulation", "type": "PROCEDURE" }, { "name": "Research Assessments and Study Monitoring", "type": "OTHER" } ], "intervention_types": [ "DRUG", "PROCEDURE", "OTHER" ], "sponsor": "Baylor College of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "21 Years", "sex": "ALL", "summary": "Up to 21 Years" }, "enrollment_count": 65, "start_date": "2024-11-01", "completion_date": "2029-08-31", "has_results": false, "last_update_posted_date": "2026-11-05", "last_synced_at": "2026-11-11T08:47:25.637Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06606574" }, { "nct_id": "NCT03560635", "title": "Feasibility and Preliminary Efficacy of a Reverse Diet as a Novel Weight Loss Maintenance Strategy for Weight-Reduced Adults With Overweight/Obesity", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Overweight and Obesity", "Weight Loss Maintenance", "Dietary Habits" ], "interventions": [ { "name": "Weight Loss Maintenance (Control vs. Reverse Diet)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "21 Years to 70 Years" }, "enrollment_count": 24, "start_date": "2018-02-14", "completion_date": "2022-01-25", "has_results": false, "last_update_posted_date": "2022-04-19", "last_synced_at": "2026-11-11T08:47:25.637Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT03560635" }, { "nct_id": "NCT05283200", "title": "Creating a Healthy L.I.F.E: Lifestyle Interventions For Epilepsy", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lifestyle" ], "interventions": [ { "name": "Yoga", "type": "BEHAVIORAL" }, { "name": "Cognitive Behavioral Therapy", "type": "BEHAVIORAL" }, { "name": "Music", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Imad Najm MD", "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": 1000, "start_date": "2022-02-11", "completion_date": "2028-06", "has_results": false, "last_update_posted_date": "2026-07-15", "last_synced_at": "2026-11-11T08:47:25.637Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05283200" }, { "nct_id": "NCT00681200", "title": "Evaluating Mechanisms of Blood Pressure Reduction Using Meditation in Hypertensive African Americans", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypertension" ], "interventions": [ { "name": "Enhanced health education", "type": "BEHAVIORAL" }, { "name": "Transcendental Meditation program", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Maharishi International University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 152, "start_date": "2008-04", "completion_date": "2012-05", "has_results": false, "last_update_posted_date": "2022-04-14", "last_synced_at": "2026-11-11T08:47:25.637Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT00681200" } ] }