Developing Biomarker-Supported Schizophrenia Spectrum Disorder (SSD) Prevention
Part of paid clinical trials in Houston, Texas.
- Sponsor
- The University of Texas Health Science Center, Houston
- Study ID
- NCT07743645
- Status
- Recruiting
Conditions
- Schizophrenia Spectrum Disorders (SSD)
Eligibility Criteria
- Sex
- ALL
- Age
- 9 Years - 19 Years
- Healthy Volunteers
- Accepted
Interventions
- Psychosocial intervention group — BEHAVIORALOver 16 weeks, participants and their parent/legal guardian(s)/caregiver(s) will attend weekly hour long family-based psychosocial intervention to work on their top 2 modifiable SSD-risk factors targeted by the risk reduction therapy (RRT)
Study Details
The purpose of this study is to compare the effect of a brief family-based psychosocial intervention that addresses modifiable SSD risk factors on persistent and distressing psychotic-like experiences in children and young adults with a family history of SSD and high versus low baseline SSD-like brain patterns
Key Dates
- First listed
- Aug 4, 2026
- Start date
- Sep 1, 2026
- Status verified
- Jul 2026
- Primary completion
- Apr 1, 2031
- Completion
- Apr 1, 2031
Study Design
- Enrollment
- 100 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- PREVENTION
Arms
- Experimental: Psychosocial intervention group
Primary Outcome Measure
Change in persistent distressing psychotic-like experiences as assessed by a modified Prodromal Questionnaire Brief-Child Version (PQ-BC) questionnaire [ Time Frame: Baseline, 8 weeks, end of intervention (16 weeks after baseline ), 1-year follow up ]
Central Contacts
- Yizhou Ma, PhD713-486-2740
- Oluwabunmi Akindona, BA713-486-2740
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The University of Texas Health Science Center at Houston | Houston | Texas | 77030 |