{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Brief+Supportive+and+Behavioral+Treatment&page=6",
    "query": {
      "intervention": "Brief Supportive and Behavioral Treatment",
      "page": 6
    },
    "page_size": 10
  },
  "pagination": {
    "page": 6,
    "page_size": 10,
    "total_count": 356,
    "total_pages": 36,
    "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Brief+Supportive+and+Behavioral+Treatment&page=7&page_size=10",
    "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Brief+Supportive+and+Behavioral+Treatment&page=5&page_size=10"
  },
  "source": "remote",
  "last_synced_at": "2026-10-06T15:18:00.643Z",
  "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": "NCT04839978",
      "title": "Community Trial in the Cherokee Nation",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Opioid Abuse"
      ],
      "interventions": [
        {
          "name": "Connect Program",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Communities Mobilizing for Change and Action (CMCA)",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "Emory University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "15 Years",
        "maximum_age": "17 Years",
        "sex": "ALL",
        "summary": "15 Years to 17 Years"
      },
      "enrollment_count": 919,
      "start_date": "2021-09-29",
      "completion_date": "2024-12-31",
      "has_results": true,
      "last_update_posted_date": "2026-03-05",
      "last_synced_at": "2026-10-06T15:18:00.643Z",
      "location_count": 1,
      "location_summary": "Tahlequah, Oklahoma",
      "locations": [
        {
          "city": "Tahlequah",
          "state": "Oklahoma"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04839978"
    },
    {
      "nct_id": "NCT02494050",
      "title": "Telemedicine for Women With Anhedonia in Bipolar and Unipolar Disorder",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Depression",
        "Bipolar Disorder",
        "Anhedonia"
      ],
      "interventions": [
        {
          "name": "Behavioral Activation-Full",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Behavioral Activation-Short",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Bipolar Disorder Collaborative Care",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "Northwestern University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "21 Years",
        "maximum_age": "65 Years",
        "sex": "FEMALE",
        "summary": "21 Years to 65 Years · Female only"
      },
      "enrollment_count": 17,
      "start_date": "2015-06",
      "completion_date": "2016-08",
      "has_results": false,
      "last_update_posted_date": "2016-09-30",
      "last_synced_at": "2026-10-06T15:18:00.643Z",
      "location_count": 1,
      "location_summary": "Chicago, Illinois",
      "locations": [
        {
          "city": "Chicago",
          "state": "Illinois"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02494050"
    },
    {
      "nct_id": "NCT03837392",
      "title": "Efficacy of Brief Acceptance and Commitment Therapy (ACT) for Perinatal Anxiety",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Post Partum Depression",
        "Perinatal Depression",
        "Post Partum Anxiety",
        "Perinatal Anxiety"
      ],
      "interventions": [
        {
          "name": "Baseline Assessment (18-26 weeks pregnant)",
          "type": "DIAGNOSTIC_TEST"
        },
        {
          "name": "Online Intervention and Phone Coaching Interventions",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Follow Up Assessments: 34-36 weeks pregnant and 4-week postpartum",
          "type": "DIAGNOSTIC_TEST"
        },
        {
          "name": "Follow Up Assessments: 8 weeks postpartum",
          "type": "DIAGNOSTIC_TEST"
        }
      ],
      "intervention_types": [
        "DIAGNOSTIC_TEST",
        "BEHAVIORAL"
      ],
      "sponsor": "University of Iowa",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "45 Years",
        "sex": "FEMALE",
        "summary": "18 Years to 45 Years · Female only"
      },
      "enrollment_count": 30,
      "start_date": "2020-06-01",
      "completion_date": "2023-06-30",
      "has_results": false,
      "last_update_posted_date": "2023-07-12",
      "last_synced_at": "2026-10-06T15:18:00.643Z",
      "location_count": 1,
      "location_summary": "Iowa City, Iowa",
      "locations": [
        {
          "city": "Iowa City",
          "state": "Iowa"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03837392"
    },
    {
      "nct_id": "NCT04693858",
      "title": "Efficacy Trial of the CALM Intervention",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Anxiety Disorder of Childhood"
      ],
      "interventions": [
        {
          "name": "Child Anxiety Learning Modules (CALM)",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Child Anxiety Learning Modules--Relaxation (CALM-R)",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "UConn Health",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "5 Years",
        "maximum_age": "12 Years",
        "sex": "ALL",
        "summary": "5 Years to 12 Years"
      },
      "enrollment_count": 218,
      "start_date": "2020-12-01",
      "completion_date": "2027-08-30",
      "has_results": false,
      "last_update_posted_date": "2026-08-12",
      "last_synced_at": "2026-10-06T15:18:00.643Z",
      "location_count": 2,
      "location_summary": "West Hartford, Connecticut • Columbia, Maryland",
      "locations": [
        {
          "city": "West Hartford",
          "state": "Connecticut"
        },
        {
          "city": "Columbia",
          "state": "Maryland"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04693858"
    },
    {
      "nct_id": "NCT04889755",
      "title": "SibACCESS: Developing a Telehealth Intervention to Address Unmet Psychosocial Needs of Siblings of Children With Cancer",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Siblings",
        "Childhood Cancer",
        "Pediatric Cancer",
        "Posttraumatic Stress Disorder"
      ],
      "interventions": [
        {
          "name": "SibACCESS",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "Boston University Charles River Campus",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "12 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "12 Years and older"
      },
      "enrollment_count": 6,
      "start_date": "2023-02-01",
      "completion_date": "2023-06-10",
      "has_results": true,
      "last_update_posted_date": "2025-02-17",
      "last_synced_at": "2026-10-06T15:18:00.643Z",
      "location_count": 1,
      "location_summary": "Boston, Massachusetts",
      "locations": [
        {
          "city": "Boston",
          "state": "Massachusetts"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04889755"
    },
    {
      "nct_id": "NCT06151158",
      "title": "Preventing Suicidal Behavior With Diverse High-Risk Youth in Acute Care Settings",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Suicide, Attempted",
        "Suicide Ideation",
        "Suicide",
        "Suicide Prevention"
      ],
      "interventions": [
        {
          "name": "Stanley Brown Safety Planning Intervention and Follow-up Contacts (SPI+)",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Interpersonal Psychotherapy for Adolescents Ultra Short Crisis Intervention (IPT-A SCI)",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "Johns Hopkins University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "12 Years",
        "maximum_age": "24 Years",
        "sex": "ALL",
        "summary": "12 Years to 24 Years"
      },
      "enrollment_count": 484,
      "start_date": "2025-03-10",
      "completion_date": "2029-08-15",
      "has_results": false,
      "last_update_posted_date": "2026-07-08",
      "last_synced_at": "2026-10-06T15:18:00.643Z",
      "location_count": 6,
      "location_summary": "St. Petersburg, Florida • Baltimore, Maryland • New York, New York + 2 more",
      "locations": [
        {
          "city": "St. Petersburg",
          "state": "Florida"
        },
        {
          "city": "Baltimore",
          "state": "Maryland"
        },
        {
          "city": "New York",
          "state": "New York"
        },
        {
          "city": "New York",
          "state": "New York"
        },
        {
          "city": "Chapel Hill",
          "state": "North Carolina"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06151158"
    },
    {
      "nct_id": "NCT04784585",
      "title": "Miro-randomized Trial for Optimizing a JITAI to Reduce Dietary Lapses in Obesity Treatment",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Obesity"
      ],
      "interventions": [
        {
          "name": "JITAI Enhanced Education Intervention Option",
          "type": "BEHAVIORAL"
        },
        {
          "name": "JITAI Self-Efficacy Intervention Option",
          "type": "BEHAVIORAL"
        },
        {
          "name": "JITAI Motivation Intervention Option",
          "type": "BEHAVIORAL"
        },
        {
          "name": "JITAI Self-Regulation Intervention Option",
          "type": "BEHAVIORAL"
        },
        {
          "name": "JITAI Generic Risk Alert Intervention Option (Active Comparator)",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Online Behavioral Obesity Treatment",
          "type": "BEHAVIORAL"
        },
        {
          "name": "JITAI No Treatment Intervention Option",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "The Miriam Hospital",
      "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": 204,
      "start_date": "2021-10-26",
      "completion_date": "2026-05-31",
      "has_results": false,
      "last_update_posted_date": "2026-05-22",
      "last_synced_at": "2026-10-06T15:18:00.643Z",
      "location_count": 1,
      "location_summary": "Providence, Rhode Island",
      "locations": [
        {
          "city": "Providence",
          "state": "Rhode Island"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04784585"
    },
    {
      "nct_id": "NCT03609450",
      "title": "Integrating Mindfulness Into the Patient-Centered Medical Home (Phase 3)",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Depression",
        "Anxiety Disorders",
        "Stress Related Disorder",
        "Adjustment Disorders",
        "Chronic Illness"
      ],
      "interventions": [
        {
          "name": "Mindfulness Training for Primary Care",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Low-Dose Comparator",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "Cambridge Health Alliance",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 96,
      "start_date": "2019-01-30",
      "completion_date": "2020-08-01",
      "has_results": false,
      "last_update_posted_date": "2020-11-20",
      "last_synced_at": "2026-10-06T15:18:00.643Z",
      "location_count": 1,
      "location_summary": "Somerville, Massachusetts",
      "locations": [
        {
          "city": "Somerville",
          "state": "Massachusetts"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03609450"
    },
    {
      "nct_id": "NCT05624931",
      "title": "Reducing Psychological Barriers to PrEP Persistence Among Pregnant and Postpartum Women in Cape Town, South Africa",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Depression",
        "Posttraumatic Stress Disorder",
        "Pregnancy Related",
        "Medication Adherence"
      ],
      "interventions": [
        {
          "name": "Brief CBT-Based Intervention",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Enhanced Treatment as Usual",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL",
        "OTHER"
      ],
      "sponsor": "Boston University Charles River Campus",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "15 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "15 Years and older · Female only"
      },
      "enrollment_count": 118,
      "start_date": "2025-04-17",
      "completion_date": "2027-07-30",
      "has_results": false,
      "last_update_posted_date": "2026-07-17",
      "last_synced_at": "2026-10-06T15:18:00.643Z",
      "location_count": 1,
      "location_summary": "Boston, Massachusetts",
      "locations": [
        {
          "city": "Boston",
          "state": "Massachusetts"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05624931"
    },
    {
      "nct_id": "NCT06998966",
      "title": "Optimizing Proton Pump Inhibitors (PPI) Prescribing With EHR-Based Decision Support",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Prescribing Patterns, Physician",
        "Physician's Practice Patterns",
        "Drug Utilization Review"
      ],
      "interventions": [
        {
          "name": "Algorithmic Defaulting (Indication-Based Default)",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Active Physician Choice",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "University of California, Los Angeles",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "50 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "50 Years and older"
      },
      "enrollment_count": 372,
      "start_date": "2026-06",
      "completion_date": "2027-06",
      "has_results": false,
      "last_update_posted_date": "2026-04-29",
      "last_synced_at": "2026-10-06T15:18:00.643Z",
      "location_count": 1,
      "location_summary": "Los Angeles, California",
      "locations": [
        {
          "city": "Los Angeles",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06998966"
    }
  ]
}