{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=surveys+and+cognitive+tests&page=2", "query": { "intervention": "surveys and cognitive tests", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 105, "total_pages": 11, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=surveys+and+cognitive+tests&page=3&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=surveys+and+cognitive+tests&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-09T07:25:07.713Z", "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": "NCT07071350", "title": "Randomized Controlled Trial of Treatment to Optimize Heart Rate Variability for Persistent Post-Concussion Symptoms", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Autonomic Nervous System Disease", "Concussive Injury", "Mild Traumatic Brain Injury", "Post Traumatic Stress Disorder", "Persistent Post Concussion Syndrome" ], "interventions": [ { "name": "HRV Coherence Ratio", "type": "OTHER" }, { "name": "NSI", "type": "BEHAVIORAL" }, { "name": "Pittsburgh Sleep Quality Index (PSQI)", "type": "BEHAVIORAL" }, { "name": "Quantitative Sleep Measures", "type": "BEHAVIORAL" }, { "name": "Patient Global Impression of Change (PGIC)", "type": "BEHAVIORAL" }, { "name": "Cognitive Performance/NIH Toolbox Cognitive Battery", "type": "BEHAVIORAL" }, { "name": "Pain Interference/TBI-QoL Pain Interference Short-Form", "type": "OTHER" }, { "name": "Patient Health Questionnaire-9 (PHQ-9)", "type": "BEHAVIORAL" }, { "name": "PTSD Checklist for DSM-5 (PCL-5)", "type": "BEHAVIORAL" }, { "name": "HRV Biofeedback (HRV-B)", "type": "OTHER" }, { "name": "Psychoeducational (Edu) Comparator Intervention", "type": "OTHER" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Virginia Commonwealth University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 148, "start_date": "2025-09-02", "completion_date": "2028-09", "has_results": false, "last_update_posted_date": "2026-09-22", "last_synced_at": "2026-10-09T07:25:07.713Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07071350" }, { "nct_id": "NCT07382557", "title": "Adaptation and Pilot Testing of a Lung Cancer Screening Decision Aid for Patients From a Safety-Net Healthcare System", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lung Cancer" ], "interventions": [ { "name": "Surveys", "type": "OTHER" }, { "name": "Focus groups", "type": "OTHER" }, { "name": "Cognitive Interviews", "type": "OTHER" }, { "name": "Lung cancer screening decision aid video", "type": "BEHAVIORAL" }, { "name": "Colon cancer screening video", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "50 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "50 Years to 80 Years" }, "enrollment_count": 360, "start_date": "2022-09-29", "completion_date": "2027-02-02", "has_results": false, "last_update_posted_date": "2026-02-03", "last_synced_at": "2026-10-09T07:25:07.713Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07382557" }, { "nct_id": "NCT06090578", "title": "TabCAT Brain Health Assessment in Primary Care", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mild Cognitive Impairment", "Dementia" ], "interventions": [ { "name": "TabCAT Brain Health Assessment Clinical Pathway", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 180000, "start_date": "2023-07-27", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2025-10-31", "last_synced_at": "2026-10-09T07:25:07.713Z", "location_count": 1, "location_summary": "Pasadena, California", "locations": [ { "city": "Pasadena", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06090578" }, { "nct_id": "NCT06555094", "title": "Randomized Clinical Trial of Supplementing Brief Psychotherapy With a Mobile App", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Suicidal Ideation", "Suicide", "Suicide Attempt" ], "interventions": [ { "name": "Ecological momentary assessment (EMA)", "type": "BEHAVIORAL" }, { "name": "Treatment as usual (TAU)", "type": "BEHAVIORAL" }, { "name": "Brief skills sessions plus EMI skills practice prompts", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Rutgers, The State University of New Jersey", "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": "2024-05-14", "completion_date": "2025-01", "has_results": false, "last_update_posted_date": "2024-08-15", "last_synced_at": "2026-10-09T07:25:07.713Z", "location_count": 1, "location_summary": "Piscataway, New Jersey", "locations": [ { "city": "Piscataway", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT06555094" }, { "nct_id": "NCT04194840", "title": "Transplant Wellness Clinic for Elderly or High Risk Patients Undergoing BMT", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stem Cell Transplant Complications", "Myeloma", "Lymphoma", "Allogeneic and Autologous Stem Cell Transplant" ], "interventions": [ { "name": "physical therapy consult", "type": "OTHER" }, { "name": "Cognitive Assessment", "type": "OTHER" }, { "name": "Cancer Aging Research Group (CARG) assessment", "type": "OTHER" }, { "name": "Medication Review", "type": "OTHER" }, { "name": "Nutrition assessment", "type": "OTHER" }, { "name": "Laboratory studies", "type": "OTHER" }, { "name": "Patient satisfaction questionnaire", "type": "OTHER" }, { "name": "Physician Questionnaire", "type": "OTHER" }, { "name": "Patient follow-up questionnaire", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Case Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 20, "start_date": "2021-05-01", "completion_date": "2025-03-28", "has_results": false, "last_update_posted_date": "2025-08-05", "last_synced_at": "2026-10-09T07:25:07.713Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT04194840" }, { "nct_id": "NCT07623811", "title": "Efficacy and Safety of Acute Topical and Aromatic Essential Oil-Based Products for Cognitive Support", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Healthy" ], "interventions": [ { "name": "Placebo", "type": "OTHER" }, { "name": "Cognitive Support System", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "dōTERRA International", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "18 Years to 64 Years" }, "enrollment_count": 100, "start_date": "2026-06-10", "completion_date": "2026-12-10", "has_results": false, "last_update_posted_date": "2026-10-01", "last_synced_at": "2026-10-09T07:25:07.713Z", "location_count": 1, "location_summary": "Pleasant Grove, Utah", "locations": [ { "city": "Pleasant Grove", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT07623811" }, { "nct_id": "NCT07565584", "title": "Examining Migration, Social Bonds, Transnationalism, and HIV Prevention Pathways Among African Immigrants.", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Prevention", "HIV Testing", "Sexual and Reproductive Health" ], "interventions": [ { "name": "Relationship-Centered HIV Prevention Intervention Component (Proof-of-Concept)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "State University of New York at Buffalo", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "18 Years to 50 Years" }, "enrollment_count": 144, "start_date": "2026-08-04", "completion_date": "2027-09", "has_results": false, "last_update_posted_date": "2026-06-29", "last_synced_at": "2026-10-09T07:25:07.713Z", "location_count": 1, "location_summary": "Buffalo, New York", "locations": [ { "city": "Buffalo", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07565584" }, { "nct_id": "NCT00550134", "title": "Cognitive Changes Associated With Breast Cancer Treatment", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Cancer", "Cognitive Side Effects of Cancer Treatments", "Stage I, II and III A Breast Cancer" ], "interventions": [ { "name": "Questionnaires, MRI, Comet assay and Cell senescence", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "FEMALE", "summary": "18 Years to 70 Years · Female only" }, "enrollment_count": 53, "start_date": "2007-10-24", "completion_date": "2021-12-28", "has_results": false, "last_update_posted_date": "2021-12-30", "last_synced_at": "2026-10-09T07:25:07.713Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00550134" }, { "nct_id": "NCT05908526", "title": "Insomnia Treatment and EMA (Ecological Momentary Assessment) Outcomes", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Insomnia" ], "interventions": [ { "name": "Baseline surveys, Cognitive testing and EMAs", "type": "BEHAVIORAL" }, { "name": "Actiwatch", "type": "DEVICE" }, { "name": "suvorexant (or placebo)", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE", "DRUG", "OTHER" ], "sponsor": "University of Maryland, Baltimore", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "60 Years to 85 Years" }, "enrollment_count": 40, "start_date": "2023-10-09", "completion_date": "2024-08-08", "has_results": true, "last_update_posted_date": "2025-10-30", "last_synced_at": "2026-10-09T07:25:07.713Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT05908526" }, { "nct_id": "NCT03242213", "title": "Patient Management of Depression Through Technology: a Study of Digitally Enabled Engagement", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Major Depressive Disorder" ], "interventions": [ { "name": "Mobile App", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Wake Forest University Health Sciences", "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": 40, "start_date": "2017-07-20", "completion_date": "2019-09-09", "has_results": false, "last_update_posted_date": "2024-10-04", "last_synced_at": "2026-10-09T07:25:07.713Z", "location_count": 1, "location_summary": "Oak Lawn, Illinois", "locations": [ { "city": "Oak Lawn", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03242213" } ] }