{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Parent+Child+Relationship&page=4",
    "query": {
      "condition": "Parent Child Relationship",
      "page": 4
    },
    "page_size": 10
  },
  "pagination": {
    "page": 4,
    "page_size": 10,
    "total_count": 337,
    "total_pages": 34,
    "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Parent+Child+Relationship&page=5&page_size=10",
    "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Parent+Child+Relationship&page=3&page_size=10"
  },
  "source": "remote",
  "last_synced_at": "2026-11-15T08:13:49.758Z",
  "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": "NCT02144051",
      "title": "Phase I Open Label Dose Escalation Study to Investigate the Safety & Pharmacokinetics of AZD5312 in Patients With Androgen Receptor Tumors",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE1"
      ],
      "conditions": [
        "Advanced Solid Tumours With Androgen Receptor Pathway as a Potential Factor"
      ],
      "interventions": [
        {
          "name": "AZD5312",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "AstraZeneca",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "130 Years",
        "sex": "ALL",
        "summary": "18 Years to 130 Years"
      },
      "enrollment_count": 32,
      "start_date": "2014-05",
      "completion_date": "2016-03",
      "has_results": false,
      "last_update_posted_date": "2016-07-14",
      "last_synced_at": "2026-11-15T08:13:49.758Z",
      "location_count": 3,
      "location_summary": "Sarasota, Florida • Nashville, Tennessee • Milwaukee, Wisconsin",
      "locations": [
        {
          "city": "Sarasota",
          "state": "Florida"
        },
        {
          "city": "Nashville",
          "state": "Tennessee"
        },
        {
          "city": "Milwaukee",
          "state": "Wisconsin"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02144051"
    },
    {
      "nct_id": "NCT01313741",
      "title": "This is a 2 Year Follow up Clinical and Radiographic Analysis of a Novel All Polyethelene Glenoid Component in Standard Total Shoulder Arthroplasty.",
      "overall_status": "UNKNOWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "The Primary Disease Process Being Studied is Shoulder OA and the Effect of an All Polyethelene Glenoid Component on Shoulder Arthroplasty"
      ],
      "interventions": [
        {
          "name": "Shoulder arthroplasty with anchor peg glenoid",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Knoxville Orthopedic Clinic",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "40 Years",
        "maximum_age": "80 Years",
        "sex": "ALL",
        "summary": "40 Years to 80 Years"
      },
      "enrollment_count": 200,
      "start_date": "2011-04",
      "completion_date": "2012-04",
      "has_results": false,
      "last_update_posted_date": "2011-03-14",
      "last_synced_at": "2026-11-15T08:13:49.758Z",
      "location_count": 1,
      "location_summary": "Knoxville, Tennessee",
      "locations": [
        {
          "city": "Knoxville",
          "state": "Tennessee"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01313741"
    },
    {
      "nct_id": "NCT07622927",
      "title": "FOCUS Bipolar: Families Opening Conversations for Understanding Signs",
      "overall_status": "RECRUITING",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Bipolar Disorder (BD)",
        "Bipolar Disorder I or II",
        "Bipolar Disorder Family Members",
        "Screening Tool"
      ],
      "interventions": [
        {
          "name": "Co-design Workshop (Observational Procedure)",
          "type": "OTHER"
        },
        {
          "name": "Alpha Testing (Observational Procedure)",
          "type": "OTHER"
        },
        {
          "name": "Beta Testing (Observational Procedure)",
          "type": "OTHER"
        },
        {
          "name": "Youth Screening Pathway & Brief Follow-Up Interview (Observational Procedure)",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "University of Texas Southwestern Medical Center",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "7 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "7 Years and older"
      },
      "enrollment_count": 200,
      "start_date": "2026-03-11",
      "completion_date": "2027-07-31",
      "has_results": false,
      "last_update_posted_date": "2026-06-03",
      "last_synced_at": "2026-11-15T08:13:49.758Z",
      "location_count": 1,
      "location_summary": "Dallas, Texas",
      "locations": [
        {
          "city": "Dallas",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT07622927"
    },
    {
      "nct_id": "NCT06391229",
      "title": "Examine the Feasibility and Acceptability of Project Support",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Parent-Child Relations",
        "Parenting",
        "Child Mental Disorder"
      ],
      "interventions": [
        {
          "name": "Project Support",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "Medical University of South Carolina",
      "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": 32,
      "start_date": "2024-07-02",
      "completion_date": "2025-06-03",
      "has_results": true,
      "last_update_posted_date": "2026-07-15",
      "last_synced_at": "2026-11-15T08:13:49.758Z",
      "location_count": 1,
      "location_summary": "Charleston, South Carolina",
      "locations": [
        {
          "city": "Charleston",
          "state": "South Carolina"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06391229"
    },
    {
      "nct_id": "NCT04829162",
      "title": "Weight Stigma by Association in Parent-Child Dyads",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Childhood Obesity",
        "Obesity"
      ],
      "interventions": [
        {
          "name": "Mother with obesity, daughter with obesity",
          "type": "OTHER"
        },
        {
          "name": "Mother with obesity, daughter without obesity",
          "type": "OTHER"
        },
        {
          "name": "Mother without obesity, daughter with obesity",
          "type": "OTHER"
        },
        {
          "name": "Mother without obesity, daughter without obesity",
          "type": "OTHER"
        },
        {
          "name": "Mother with obesity, son with obesity",
          "type": "OTHER"
        },
        {
          "name": "Mother with obesity, son without obesity",
          "type": "OTHER"
        },
        {
          "name": "Mother without obesity, son with obesity",
          "type": "OTHER"
        },
        {
          "name": "Mother without obesity, son without obesity",
          "type": "OTHER"
        },
        {
          "name": "Father with obesity, daughter with obesity",
          "type": "OTHER"
        },
        {
          "name": "Father with obesity, daughter without obesity",
          "type": "OTHER"
        },
        {
          "name": "Father without obesity, daughter with obesity",
          "type": "OTHER"
        },
        {
          "name": "Father without obesity, daughter without obesity",
          "type": "OTHER"
        },
        {
          "name": "Father with obesity, son with obesity",
          "type": "OTHER"
        },
        {
          "name": "Father with obesity, son without obesity",
          "type": "OTHER"
        },
        {
          "name": "Father without obesity, son with obesity",
          "type": "OTHER"
        },
        {
          "name": "Father without obesity, son without obesity",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "University of California, Los Angeles",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 1973,
      "start_date": "2020-02-21",
      "completion_date": "2020-02-21",
      "has_results": false,
      "last_update_posted_date": "2021-04-02",
      "last_synced_at": "2026-11-15T08:13:49.758Z",
      "location_count": 1,
      "location_summary": "Los Angeles, California",
      "locations": [
        {
          "city": "Los Angeles",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04829162"
    },
    {
      "nct_id": "NCT07490535",
      "title": "This is a Single Center, Open-label Prospective Study to Evaluate the Effect of Xiidra® (Lifitegrast Ophthalmic Solution 5.0%) on Tear Film Biomarkers in Dry Eye",
      "overall_status": "NOT_YET_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Ocular Surface Disease",
        "Dry Eye Syndrome (DES)"
      ],
      "interventions": [
        {
          "name": "(Xiidra®) Lifitegrast Ophthalmic Solution 5.0%",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Pittsburgh Research Institute",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 36,
      "start_date": "2026-03",
      "completion_date": "2026-11",
      "has_results": false,
      "last_update_posted_date": "2026-03-24",
      "last_synced_at": "2026-11-15T08:13:49.758Z",
      "location_count": 1,
      "location_summary": "Sewickley, Pennsylvania",
      "locations": [
        {
          "city": "Sewickley",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT07490535"
    },
    {
      "nct_id": "NCT04627415",
      "title": "Project PEAK: Early Intervention for ADHD",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Attention Deficit Hyperactivity Disorder",
        "Parent-Child Relations",
        "Child Behavior",
        "Parenting"
      ],
      "interventions": [
        {
          "name": "Promoting Engagement with ADHD Pre-Kindergarteners",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "Lehigh University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "3 Years",
        "maximum_age": "5 Years",
        "sex": "ALL",
        "summary": "3 Years to 5 Years"
      },
      "enrollment_count": 180,
      "start_date": "2020-09-01",
      "completion_date": "2026-12-31",
      "has_results": false,
      "last_update_posted_date": "2025-09-09",
      "last_synced_at": "2026-11-15T08:13:49.758Z",
      "location_count": 1,
      "location_summary": "Bethlehem, Pennsylvania",
      "locations": [
        {
          "city": "Bethlehem",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04627415"
    },
    {
      "nct_id": "NCT06505811",
      "title": "Mixed Methods Evaluation of the Pomona Household Universal Grant (HUG) Program",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Early Child Well-being",
        "Parental Stress",
        "Family Economic Security",
        "Parental/Caregiver Health",
        "Mental Health"
      ],
      "interventions": [
        {
          "name": "Guaranteed Income ($500/monthly)",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Active Comparison ($20/monthly)",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "University of California, Los Angeles",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 599,
      "start_date": "2024-06-17",
      "completion_date": "2025-12-31",
      "has_results": false,
      "last_update_posted_date": "2026-09-09",
      "last_synced_at": "2026-11-15T08:13:49.758Z",
      "location_count": 1,
      "location_summary": "Los Angeles, California",
      "locations": [
        {
          "city": "Los Angeles",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06505811"
    },
    {
      "nct_id": "NCT06532032",
      "title": "A Study of Combination Therapy With Amivantamab and Docetaxel in Participants With Metastatic Non-small Cell Lung Cancer",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE1",
        "PHASE2"
      ],
      "conditions": [
        "Carcinoma, Non-Small-Cell Lung"
      ],
      "interventions": [
        {
          "name": "Amivantamab",
          "type": "DRUG"
        },
        {
          "name": "Docetaxel",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Janssen Research & Development, LLC",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 12,
      "start_date": "2024-07-23",
      "completion_date": "2026-05-14",
      "has_results": false,
      "last_update_posted_date": "2026-07-31",
      "last_synced_at": "2026-11-15T08:13:49.758Z",
      "location_count": 6,
      "location_summary": "Irvine, California • Los Alamitos, California • Orange, California + 3 more",
      "locations": [
        {
          "city": "Irvine",
          "state": "California"
        },
        {
          "city": "Los Alamitos",
          "state": "California"
        },
        {
          "city": "Orange",
          "state": "California"
        },
        {
          "city": "Springfield",
          "state": "Missouri"
        },
        {
          "city": "Flemington",
          "state": "New Jersey"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06532032"
    },
    {
      "nct_id": "NCT01901536",
      "title": "Family Foundations Coparenting Pilot Trial",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Parent-Child Relations"
      ],
      "interventions": [
        {
          "name": "Family Foundations Coparenting Program",
          "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": 497,
      "start_date": "2002-12",
      "completion_date": "2007-11",
      "has_results": false,
      "last_update_posted_date": "2021-02-08",
      "last_synced_at": "2026-11-15T08:13:49.758Z",
      "location_count": 1,
      "location_summary": "University Park, Pennsylvania",
      "locations": [
        {
          "city": "University Park",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01901536"
    }
  ]
}