{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Depression%2C+Anxiety%2C+PTSD&page=3", "query": { "condition": "Depression, Anxiety, PTSD", "page": 3 }, "page_size": 10 }, "pagination": { "page": 3, "page_size": 10, "total_count": 166, "total_pages": 17, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Depression%2C+Anxiety%2C+PTSD&page=4&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Depression%2C+Anxiety%2C+PTSD&page=2&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-02T09:22:42.445Z", "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": "NCT02024204", "title": "Uncontrolled Lower Respiratory Symptoms in the WTC Survivor Program", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lung Diseases", "Medication Compliance" ], "interventions": [ { "name": "Fluticasone propionate 230mcg for 3 Months", "type": "DRUG" }, { "name": "Current Treatment or no treatment", "type": "DRUG" }, { "name": "Salmeterol 21mcg for 3 Months", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "NYU Langone Health", "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": 60, "start_date": "2014-04-09", "completion_date": "2017-05-17", "has_results": true, "last_update_posted_date": "2021-02-02", "last_synced_at": "2026-10-02T09:22:42.445Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02024204" }, { "nct_id": "NCT01385709", "title": "The Influence of the Menstrual Cycle on Lithium and Sertraline Blood Levels", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Bipolar Affective Disorders", "Cyclothymic Disorder", "Schizoaffective Disorder", "Major Depressive Disorder", "Dysthymic Disorder", "Obsessive-Compulsive Disorder", "Panic Disorder", "Posttraumatic Stress Disorder", "Premenstrual Dysphoric Disorder", "Social Anxiety Disorder" ], "interventions": [], "intervention_types": [], "sponsor": "Weill Medical College of Cornell University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "FEMALE", "summary": "18 Years to 40 Years · Female only" }, "enrollment_count": 29, "start_date": "2008-08", "completion_date": "2013-08", "has_results": false, "last_update_posted_date": "2017-02-20", "last_synced_at": "2026-10-02T09:22:42.445Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01385709" }, { "nct_id": "NCT06583395", "title": "Quest to Analyze One Thousand Humans Meditating", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Amyotrophic Lateral Sclerosis (ALS)", "Angina, Stable", "Anxiety", "Asthma", "Atrial Fibrillation", "Cancer Brain", "Cancer, Breast", "Cancer Colon", "Cancer, Lung", "Cancer, Ovarian", "Cancer Prostate", "Cancer Skin", "Throat Cancer", "Lymphoma", "Cancer, Thyroid", "Cancer, Other", "Cerebral Palsy", "Chronic Fatigue Syndrome", "Cluster Headache", "Chronic Obstructive Pulmonary Disease (COPD)", "Chronic Kidney Diseases", "Crohn Disease", "Deafness", "Depression", "Diabetes", "Eczema", "Epilepsy", "Fibroids", "Fibromyalgia", "Heart Failure", "Hypertension", "Hyperthyroidism", "Hypothyroidism", "Irritable Bowel Syndrome (IBS)", "Infertility", "Lyme Disease", "Macular Degeneration", "Migraine", "Multiple Allergies", "Multiple Sclerosis", "Osteoarthritis", "Osteoporosis", "Ovarian Cysts", "Parkinson Disease", "Phantom Limb Pain", "Psoriasis", "Post Traumatic Stress Disorder (PTSD)", "Rheumatoid Arthritis", "Sjogrens Disease", "Spinal Cord Injury", "Spinal Stenosis", "Stroke", "Tension Headache", "Tinnitus", "Ulcerative Colitis" ], "interventions": [ { "name": "Advanced multi-component meditation practice", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Tobias Moeller-Bertram", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 3000, "start_date": "2021-12-05", "completion_date": "2025-03-25", "has_results": false, "last_update_posted_date": "2024-11-01", "last_synced_at": "2026-10-02T09:22:42.445Z", "location_count": 1, "location_summary": "Palm Desert, California", "locations": [ { "city": "Palm Desert", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06583395" }, { "nct_id": "NCT05541406", "title": "Efficacy of a Multi-level School Intervention for LGBTQ Youth", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression", "Anxiety", "Post Traumatic Stress Disorder", "Coping Behavior", "Sexual Minority Stress", "Suicidality", "Substance Use", "Bullying", "Harassment" ], "interventions": [ { "name": "Proud & Empowered", "type": "BEHAVIORAL" }, { "name": "Control Group", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Years", "maximum_age": "20 Years", "sex": "ALL", "summary": "12 Years to 20 Years" }, "enrollment_count": 228, "start_date": "2022-09-14", "completion_date": "2027-04-30", "has_results": false, "last_update_posted_date": "2026-09-11", "last_synced_at": "2026-10-02T09:22:42.445Z", "location_count": 23, "location_summary": "El Monte, California • Glendale, California • Inglewood, California + 7 more", "locations": [ { "city": "El Monte", "state": "California" }, { "city": "El Monte", "state": "California" }, { "city": "El Monte", "state": "California" }, { "city": "El Monte", "state": "California" }, { "city": "El Monte", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05541406" }, { "nct_id": "NCT00978484", "title": "A Head-to-head Comparison of Virtual Reality Treatment for Post Traumatic Stress Disorder", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Post Traumatic Stress Disorder" ], "interventions": [ { "name": "Virtual Reality Exposure Therapy - Dynamic", "type": "BEHAVIORAL" }, { "name": "Augmented Exposure Therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "United States Naval Medical Center, San Diego", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 150, "start_date": "2009-09", "completion_date": "2014-10", "has_results": false, "last_update_posted_date": "2014-06-30", "last_synced_at": "2026-10-02T09:22:42.445Z", "location_count": 2, "location_summary": "Camp Pendlton, California • San Diego, California", "locations": [ { "city": "Camp Pendlton", "state": "California" }, { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00978484" }, { "nct_id": "NCT03254719", "title": "Care Outcomes for Chiropractic Outpatient Veterans", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Low Back Pain", "PTSD", "Depression", "Anxiety" ], "interventions": [ { "name": "Study assessments", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Palmer College of Chiropractic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 40, "start_date": "2018-02-19", "completion_date": "2018-11-05", "has_results": true, "last_update_posted_date": "2020-05-18", "last_synced_at": "2026-10-02T09:22:42.445Z", "location_count": 4, "location_summary": "Coralville, Iowa • Davenport, Iowa • Iowa City, Iowa + 1 more", "locations": [ { "city": "Coralville", "state": "Iowa" }, { "city": "Davenport", "state": "Iowa" }, { "city": "Iowa City", "state": "Iowa" }, { "city": "Oskaloosa", "state": "Iowa" } ], "official_url": "https://clinicaltrials.gov/study/NCT03254719" }, { "nct_id": "NCT01277354", "title": "Effectiveness of Cognitive Processing Therapy in Pregnant Women With a History of Pregnancy Loss/Complication", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post-traumatic Stress Disorder", "Stress Disorders", "Anxiety", "Depression" ], "interventions": [ { "name": "Cognitive Processing Therapy", "type": "BEHAVIORAL" }, { "name": "Waitlist Placebo", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "49 Years", "sex": "FEMALE", "summary": "18 Years to 49 Years · Female only" }, "enrollment_count": 2, "start_date": "2010-04", "completion_date": "2011-06", "has_results": true, "last_update_posted_date": "2017-04-17", "last_synced_at": "2026-10-02T09:22:42.445Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01277354" }, { "nct_id": "NCT03077919", "title": "Effectiveness and Acceptability of Stellate Ganglion Block for Posttraumatic Stress Disorder Symptoms - Effectiveness", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "PostTraumatic Stress Disorder" ], "interventions": [ { "name": "Ropivacaine", "type": "DRUG" }, { "name": "Sham treatment", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "RTI International", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 113, "start_date": "2016-05-25", "completion_date": "2018-06-09", "has_results": true, "last_update_posted_date": "2020-05-13", "last_synced_at": "2026-10-02T09:22:42.445Z", "location_count": 2, "location_summary": "Honolulu, Hawaii • Fort Bragg, North Carolina", "locations": [ { "city": "Honolulu", "state": "Hawaii" }, { "city": "Fort Bragg", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03077919" }, { "nct_id": "NCT07452900", "title": "Using Integrated Care and Wearable Technology to Evaluate Outcomes of the Shields & Stripes Program for Veterans and First Responders", "overall_status": "NOT_YET_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Holistic Care", "Mental Health", "Sleep", "PTSD", "Depression - Major Depressive Disorder", "Anxiety", "Resilience", "Recovery", "Occupation", "Biometrics Measurement", "Veteran", "Quality of Life" ], "interventions": [], "intervention_types": [], "sponsor": "Baylor University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 80, "start_date": "2026-04-01", "completion_date": "2027-04-30", "has_results": false, "last_update_posted_date": "2026-03-10", "last_synced_at": "2026-10-02T09:22:42.445Z", "location_count": 1, "location_summary": "Waco, Texas", "locations": [ { "city": "Waco", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07452900" }, { "nct_id": "NCT07372586", "title": "Behavioral Health Collaborative Care Model in an ICU Recovery Clinic", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "PICS", "Anxiety", "Depression - Major Depressive Disorder", "Post-Traumatic Stress", "PTSD", "Critical Illness Recovery", "Critical Illness", "Collaborative Care", "Behavioral Health Concerns" ], "interventions": [ { "name": "Behavioral Health Collaborative Care Model", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Medical University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 150, "start_date": "2026-01-30", "completion_date": "2028-06-30", "has_results": false, "last_update_posted_date": "2026-03-12", "last_synced_at": "2026-10-02T09:22:42.445Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT07372586" } ] }