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Palliative Care Needs of Children With Rare Diseases and Their Families
Sponsor: Children's National Research Institute
Summary
The palliative care needs of family caregivers of children with rare diseases and their children are largely unmet, including the need for support to prepare for future medical decision making. This trial will test the FACE-Rare intervention to see if investigators can identify and meet those needs; and if FACE-Rare effects family caregivers' quality of life and child healthcare utilization. Finally, investigators will determine if the intersectionality of child-sex, family-race, Federal poverty level, and social connection influences family quality of life and child health care utilization longitudinally.
Key Details
Gender
All
Age Range
12 Months - 99 Years
Study Type
INTERVENTIONAL
Enrollment
480
Start Date
2025-10-02
Completion Date
2029-08-02
Last Updated
2026-01-28
Healthy Volunteers
Yes
Conditions
Interventions
Family Centered pediatric palliative care for family caregivers of children with rare diseases.
Child with rare disease who is unable to participate in medical decision making/family caregiver/support person triads will be randomized at a 1:1 ratio to one of two study arms, either the 3 session FACE-Rare intervention or the enhanced Treatment as Usual. Assessments will be completed at baseline, 3, 6 and 12 month outcomes.
Locations (1)
Children's National Hospital
Washington D.C., District of Columbia, United States