Comparative Effectiveness of SPARCS and Unified Protocol for Youth With Chronic Medical Conditions and Trauma-Related Distress
NCT07483333
This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
The goal of this clinical trial is to compare the effectiveness of trauma-focused therapies for improving mental health symptoms and daily functioning in youth with chronic medical conditions who have experienced psychological trauma and trauma-related distress.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Trauma Exposure
- Trauma
- Trauma and Stressor Related Disorder
- Mental Health Functioning
- Chronic Medical Conditions
- Chronic Medical Condition
- Chronic Medical Illness
- Posttraumatic Stress Disorder PTSD
- Posttraumatic Stress Disorders
- Posttraumatic Stress Symptoms
- Posttraumatic Stress
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 8 to 18 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Sponsor
- Anthony Vesco
- Last updated on ClinicalTrials.gov
- September 15, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Illinois · 1
- Ann & Robert H. Lurie Children's Hospital of Chicago · Chicago, IL
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.