{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Life+Force", "query": { "intervention": "Life Force" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 33, "total_pages": 4, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Life+Force&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-08T15:54:38.342Z", "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": "NCT03653637", "title": "Group (\"Project Life Force\") vs. Individual Suicide Safety Planning RCT", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Suicide" ], "interventions": [ { "name": "Project Life Force", "type": "BEHAVIORAL" }, { "name": "Treatment as Usual", "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": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 294, "start_date": "2018-10-15", "completion_date": "2024-03-30", "has_results": true, "last_update_posted_date": "2025-11-10", "last_synced_at": "2026-09-08T15:54:38.342Z", "location_count": 2, "location_summary": "The Bronx, New York • Philadelphia, Pennsylvania", "locations": [ { "city": "The Bronx", "state": "New York" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03653637" }, { "nct_id": "NCT06736925", "title": "Omega-3 Fatty Acids and Subconcussive Head Impacts", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Subconcussive Head Impact", "Omega-3 Fatty Acids" ], "interventions": [ { "name": "Omega-3 Fatty Acids (EPA plus DHA)", "type": "DIETARY_SUPPLEMENT" }, { "name": "Organic soybean oil", "type": "DIETARY_SUPPLEMENT" }, { "name": "Soccer Heading Model", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "30 Years", "sex": "ALL", "summary": "18 Years to 30 Years" }, "enrollment_count": 208, "start_date": "2025-02-28", "completion_date": "2029-05-31", "has_results": false, "last_update_posted_date": "2026-04-29", "last_synced_at": "2026-09-08T15:54:38.342Z", "location_count": 1, "location_summary": "Bloomington, Indiana", "locations": [ { "city": "Bloomington", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT06736925" }, { "nct_id": "NCT07401940", "title": "HAVEN-Connect Youth Suicide Prevention", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Suicide Prevention" ], "interventions": [ { "name": "HAVEN-Connect", "type": "BEHAVIORAL" }, { "name": "HAVEN Suicide Prevention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "George Washington University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "13 Years", "maximum_age": "19 Years", "sex": "ALL", "summary": "13 Years to 19 Years" }, "enrollment_count": 240, "start_date": "2023-06-01", "completion_date": "2026-11-30", "has_results": false, "last_update_posted_date": "2026-07-20", "last_synced_at": "2026-09-08T15:54:38.342Z", "location_count": 2, "location_summary": "New York, New York • Rochester, New York", "locations": [ { "city": "New York", "state": "New York" }, { "city": "Rochester", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07401940" }, { "nct_id": "NCT07050238", "title": "Evaluation of a Group-based, Skills Training for Increasing Mental Toughness", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Resilience", "Mental Toughness" ], "interventions": [ { "name": "Life Force", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Uniformed Services University of the Health Sciences", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2400, "start_date": "2026-01-06", "completion_date": "2029-07-01", "has_results": false, "last_update_posted_date": "2026-06-15", "last_synced_at": "2026-09-08T15:54:38.342Z", "location_count": 1, "location_summary": "Killeen, Texas", "locations": [ { "city": "Killeen", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07050238" }, { "nct_id": "NCT03709199", "title": "Long Term Follow up of Children Enrolled in the REDvent Study", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Respiratory Distress Syndrome, Adult", "Ventilator-Induced Lung Injury", "Neurocognitive Dysfunction", "Quality of Life", "Respiration Disorders" ], "interventions": [ { "name": "Ventilation Inhomogeneity", "type": "DIAGNOSTIC_TEST" }, { "name": "Diaphragm Ultrasound", "type": "DIAGNOSTIC_TEST" }, { "name": "Respiratory Inductance Plethysmography", "type": "DIAGNOSTIC_TEST" }, { "name": "Spirometry", "type": "DIAGNOSTIC_TEST" }, { "name": "Functional Residual Capacity", "type": "DIAGNOSTIC_TEST" }, { "name": "MIP/MEP", "type": "DIAGNOSTIC_TEST" }, { "name": "6 minute walk test", "type": "DIAGNOSTIC_TEST" }, { "name": "Neurocognitive Testing", "type": "DIAGNOSTIC_TEST" }, { "name": "Emotional Health Assessment", "type": "DIAGNOSTIC_TEST" }, { "name": "Health Related Quality of Life", "type": "DIAGNOSTIC_TEST" }, { "name": "Functional Status", "type": "DIAGNOSTIC_TEST" }, { "name": "Respiratory Status Questionnaire", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Children's Hospital Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Month", "maximum_age": "18 Years", "sex": "ALL", "summary": "1 Month to 18 Years" }, "enrollment_count": 176, "start_date": "2018-10-01", "completion_date": "2026-05-01", "has_results": false, "last_update_posted_date": "2025-04-17", "last_synced_at": "2026-09-08T15:54:38.342Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03709199" }, { "nct_id": "NCT02895503", "title": "Yoga in Improving Quality of Life in Patients With Non-small Cell Lung Cancer Undergoing Treatment", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Non-small Cell Lung Cancer", "Recurrent Non-Small Cell Lung Carcinoma" ], "interventions": [ { "name": "Yoga", "type": "BEHAVIORAL" }, { "name": "Support Group Therapy", "type": "BEHAVIORAL" }, { "name": "FACT-L", "type": "OTHER" }, { "name": "Pulmonary function test", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Virginia Commonwealth University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 1, "start_date": "2012-01", "completion_date": "2013-08", "has_results": false, "last_update_posted_date": "2016-09-09", "last_synced_at": "2026-09-08T15:54:38.342Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02895503" }, { "nct_id": "NCT02525575", "title": "Suicide Safety Planning Group Treatment: \"Project Life Force\"", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Suicide" ], "interventions": [ { "name": "Project Life Force Group Treatment", "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": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 45, "start_date": "2015-10-01", "completion_date": "2018-03-01", "has_results": true, "last_update_posted_date": "2019-10-25", "last_synced_at": "2026-09-08T15:54:38.342Z", "location_count": 1, "location_summary": "The Bronx, New York", "locations": [ { "city": "The Bronx", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02525575" }, { "nct_id": "NCT02710162", "title": "Accurate Screening Tools for Dysphagia in Amyotrophic Lateral Sclerosis (ALS)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Amyotrophic Lateral Sclerosis" ], "interventions": [ { "name": "Micro Mouth Pressure Meter", "type": "DEVICE" }, { "name": "Iowa Oral Performance Instrument", "type": "DEVICE" }, { "name": "Electrical Impedance Myography", "type": "DEVICE" }, { "name": "Capsaicin", "type": "DRUG" }, { "name": "Videofluoroscopic Swallowing Study", "type": "PROCEDURE" }, { "name": "Pulmonary Function Testing", "type": "PROCEDURE" }, { "name": "Swallowing Related Quality of Life Questionnaire", "type": "OTHER" }, { "name": "Functional Oral Intake Scale", "type": "OTHER" }, { "name": "Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised", "type": "OTHER" }, { "name": "Eating Assessment Tool-10", "type": "OTHER" }, { "name": "Communicative Effectiveness Survey", "type": "OTHER" }, { "name": "The Center for Neurologic Studies Bulbar Function Scale", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "DRUG", "PROCEDURE", "OTHER" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "21 Years to 85 Years" }, "enrollment_count": 21, "start_date": "2016-04", "completion_date": "2017-12-19", "has_results": false, "last_update_posted_date": "2017-12-21", "last_synced_at": "2026-09-08T15:54:38.342Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02710162" }, { "nct_id": "NCT07637838", "title": "Characterizing the Effects of Platelet-Rich Fibrin (PRF) as a Palatal Wound Dressing on Quality of Life and Sleep Following Mucogingival Surgery. Study Was Conducted at the Air Force Post Graduate Dental School. All HIPPA Consents and Research Informed Consents Are Located at JBSA-Lackland.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Palatal Donor Site Wound Healing", "Platelet Rich Fibrin", "Sleep Quality", "Pain", "Analgesic Consumption" ], "interventions": [ { "name": "Platelet rich fibrin", "type": "PROCEDURE" }, { "name": "Control Group: collagen matrices or oxidized cellulose membrane", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "59th Medical Wing", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 78, "start_date": "2024-05-24", "completion_date": "2025-03-18", "has_results": false, "last_update_posted_date": "2026-06-10", "last_synced_at": "2026-09-08T15:54:38.342Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07637838" }, { "nct_id": "NCT06591780", "title": "Innovative Multi-Variable Biofeedback for Improving Gait Performance in Individuals With Diabetic Peripheral Neuropathy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetic Peripheral Neuropathy", "Diabetes Mellitus" ], "interventions": [ { "name": "Clinical Evaluation", "type": "OTHER" }, { "name": "Plantar Pressure Biofeedback Gait Training", "type": "OTHER" }, { "name": "Propulsion Biofeedback Gait Training", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Florida Institute for Human and Machine Cognition", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "45 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "45 Years to 90 Years" }, "enrollment_count": 25, "start_date": "2025-10-20", "completion_date": "2027-06-01", "has_results": false, "last_update_posted_date": "2026-03-11", "last_synced_at": "2026-09-08T15:54:38.342Z", "location_count": 1, "location_summary": "Pensacola, Florida", "locations": [ { "city": "Pensacola", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06591780" } ] }