{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Personal+Satisfaction&page=2", "query": { "condition": "Personal Satisfaction", "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?condition=Personal+Satisfaction&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-06-10T18:25:39.974Z", "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": "NCT06644573", "title": "Evaluating the Efficacy and Safety of PROSOMNIA Sleep Therapy™ in Patients With Sleep Deprivation and Chronic Insomnia", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Chronic Insomnia", "Sleep Deprivation", "REM Behavior Disorder", "REM Sleep Behavior Disorder", "REM Sleep Measurement", "Insomnia", "Insomnia Related to Specified Disorder", "Insomnia Due to Other Mental Disorder", "Insomnia Comorbid to Psychiatric Disorder", "Insomnia Due to Anxiety and Fear", "Insomnia Related to Another Mental Condition", "Insomnia Disorders", "Idiopathic Hypersomnia", "Sleep Disorders, Circadian Rhythm", "Post Trauma Nightmares", "PTSD - Post Traumatic Stress Disorder", "Sleep Quality", "Anesthesia", "Anxiety", "Depression", "Mental Health", "Alzheimer Disease or Associated Disorder", "Parkinsons", "Circadian Rhythm", "Circadian Dysregulation", "PTSD", "Post-Traumatic", "Post-Traumatic Stress Disorder Complex", "Military Combat Stress Reaction", "Sleep", "Military Activity", "Veterans", "Shift Work Sleep Disorder", "Menopause Related Conditions", "Pain", "Cancer Pain", "Athletes" ], "interventions": [ { "name": "PROSOMNIA Sleep Therapy™ (PSTx)", "type": "PROCEDURE" }, { "name": "Anesthesia-Induced Sleep Therapy", "type": "PROCEDURE" }, { "name": "Diprivan (propofol), Astra-Zeneca", "type": "DRUG" }, { "name": "Continuous EEG Monitoring", "type": "DEVICE" } ], "intervention_types": [ "PROCEDURE", "DRUG", "DEVICE" ], "sponsor": "Nyree Penn", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 100, "start_date": "2025-11-01", "completion_date": "2026-05-01", "has_results": false, "last_update_posted_date": "2025-05-28", "last_synced_at": "2026-06-10T18:25:39.974Z", "location_count": 1, "location_summary": "Aventura, Florida", "locations": [ { "city": "Aventura", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06644573" }, { "nct_id": "NCT06667479", "title": "Cold Water Exposure and Immune Function Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cold Water Immersion", "Immune Function", "Muscular Strength", "Mental Health" ], "interventions": [ { "name": "Cold Water Immersion (CWI) - Cold Tub Immersion (CI)", "type": "OTHER" }, { "name": "Cold Water Immersion (CWI) - Cold Shower (CS)", "type": "OTHER" }, { "name": "Control Group (CO)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Northern Colorado", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "18 Years to 45 Years" }, "enrollment_count": 37, "start_date": "2024-10-10", "completion_date": "2026-03-01", "has_results": false, "last_update_posted_date": "2026-03-10", "last_synced_at": "2026-06-10T18:25:39.974Z", "location_count": 1, "location_summary": "Greeley, Colorado", "locations": [ { "city": "Greeley", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT06667479" }, { "nct_id": "NCT04806620", "title": "Unhide® Project: A Digital Health Platform to Collect Lifestyle Data for Brain Inflammation Research", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Post-Acute COVID-19 Syndrome", "ME/CFS", "Rheumatic Arthritis", "Juvenile Rheumatoid Arthritis (JRA)", "Psoriatic Arthritis (PsA)", "Ankylosing Spondylitis (AS)", "Autoimmune Encephalitis", "Celiac Disease", "Celiac Disease in Children", "Chronic Lyme Disease", "Post-treatment Lyme Disease Syndrome", "Crohn's Disease", "Dysautonomia", "Anorexia Nervosa", "Bulimia Nervosa", "ARFID", "Avoidant / Restrictive Food Intake Disorder", "Ehlers Danlos Syndrome", "Endometriosis", "Fibromyalgia (FM)", "Long COVID", "Lupus", "Migraines", "Mast Cell Activation Syndrome", "Multiple Sclerosis", "Myalgic Encephalomyelitis (ME)", "Myasthenia Gravis, Generalized", "Myasthenia Gravis in Children", "Narcolepsy", "Obsessive Compulsive Disorder (OCD)", "PANDAS", "Pediatric Acute-onset Neuropsychiatric Syndrome (PANS)", "POTS - Postural Orthostatic Tachycardia Syndrome", "General Anxiety Disorder, Social Anxiety Disorder", "PTSD - Post Traumatic Stress Disorder", "Psoriasis", "Traumatic Brain Injury", "Tourette's Syndrome", "Inflammatory Bowel Disease (IBD)", "Autoimmune Diseases", "Neurological Diseases or Conditions", "Psychiatric Disorder", "Sjogren's Syndrome", "Ulcerative Colitis and Crohn's Disease" ], "interventions": [], "intervention_types": [], "sponsor": "Brain Inflammation Collaborative", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "2 Years", "maximum_age": null, "sex": "ALL", "summary": "2 Years and older" }, "enrollment_count": 10000, "start_date": "2023-07-05", "completion_date": "2030-12-31", "has_results": false, "last_update_posted_date": "2026-01-22", "last_synced_at": "2026-06-10T18:25:39.974Z", "location_count": 1, "location_summary": "Delafield, Wisconsin", "locations": [ { "city": "Delafield", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT04806620" }, { "nct_id": "NCT03624868", "title": "Tai Chi and Wellness Education for Older Veterans", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Physical Activity", "PTSD", "Satisfaction" ], "interventions": [ { "name": "Tai Chi", "type": "BEHAVIORAL" }, { "name": "Wellness Education", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "VA Boston Healthcare System", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "60 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "60 Years to 100 Years" }, "enrollment_count": 24, "start_date": "2019-01-29", "completion_date": "2022-04-20", "has_results": false, "last_update_posted_date": "2025-04-03", "last_synced_at": "2026-06-10T18:25:39.974Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03624868" }, { "nct_id": "NCT00983476", "title": "Web-Based Delivery of MOVE! to Veterans With Serious Mental Illness (SMI)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Psychotic Disorders", "Obesity", "Health Behaviors" ], "interventions": [ { "name": "in-person MOVE! SMI", "type": "BEHAVIORAL" }, { "name": "web-based MOVE! SMI", "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": 276, "start_date": "2012-03", "completion_date": "2015-06", "has_results": true, "last_update_posted_date": "2017-04-13", "last_synced_at": "2026-06-10T18:25:39.974Z", "location_count": 1, "location_summary": "West Los Angeles, California", "locations": [ { "city": "West Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00983476" }, { "nct_id": "NCT07331922", "title": "Mental Health App and Impact on Wellbeing", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Well-Being, Psychological" ], "interventions": [ { "name": "mental health app", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Penn State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 160, "start_date": "2026-08", "completion_date": "2027-05", "has_results": false, "last_update_posted_date": "2026-05-06", "last_synced_at": "2026-06-10T18:25:39.974Z", "location_count": 1, "location_summary": "Erie, Pennsylvania", "locations": [ { "city": "Erie", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07331922" }, { "nct_id": "NCT07306013", "title": "The SolanoConnex Trial: Evaluation of a Mental Health Access Project", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mental Health" ], "interventions": [ { "name": "Access to the SolanoConnex.org", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Touro University, California", "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": "2025-07-13", "completion_date": "2026-06-30", "has_results": false, "last_update_posted_date": "2025-12-26", "last_synced_at": "2026-06-10T18:25:39.974Z", "location_count": 1, "location_summary": "Vallejo, California", "locations": [ { "city": "Vallejo", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07306013" }, { "nct_id": "NCT04968496", "title": "Biobehavioral Mechanisms of Food Insecurity", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Food Insecurity", "Obesity, Childhood", "Inflammation", "Mental Health" ], "interventions": [ { "name": "Food Secure Group", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "The Miriam Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "8 Years", "maximum_age": "12 Years", "sex": "ALL", "summary": "8 Years to 12 Years" }, "enrollment_count": 9, "start_date": "2022-05-24", "completion_date": "2023-01-24", "has_results": false, "last_update_posted_date": "2023-01-26", "last_synced_at": "2026-06-10T18:25:39.974Z", "location_count": 1, "location_summary": "Newport, Rhode Island", "locations": [ { "city": "Newport", "state": "Rhode Island" } ], "official_url": "https://clinicaltrials.gov/study/NCT04968496" }, { "nct_id": "NCT01156727", "title": "Linking National Guard Veterans With Need to Mental Health Care", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Healthy" ], "interventions": [], "intervention_types": [], "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": 3015, "start_date": "2010-07-01", "completion_date": "2014-05-30", "has_results": false, "last_update_posted_date": "2017-06-06", "last_synced_at": "2026-06-10T18:25:39.974Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT01156727" }, { "nct_id": "NCT05554042", "title": "Kintsugi Voice Device Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Depression, Anxiety" ], "interventions": [ { "name": "Kintsugi Voice Device", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Kintsugi Mindful Wellness, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "22 Years", "maximum_age": null, "sex": "ALL", "summary": "22 Years and older" }, "enrollment_count": 132, "start_date": "2022-09-23", "completion_date": "2023-07-05", "has_results": false, "last_update_posted_date": "2024-02-12", "last_synced_at": "2026-06-10T18:25:39.974Z", "location_count": 1, "location_summary": "Berkeley, California", "locations": [ { "city": "Berkeley", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05554042" } ] }