Actively Recruiting
Context-Aware Mobile Intervention for Social Recovery in Serious Mental Illness (R33)
Led by University of California, San Diego · Updated on 2026-02-23
125
Participants Needed
1
Research Sites
169 weeks
Total Duration
On this page
Sponsors
U
University of California, San Diego
Lead Sponsor
N
National Institute of Mental Health (NIMH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This randomized clinical trial will test a new technology-supported blended intervention, mobile Social Interaction Therapy by Exposure (mSITE), that targets social engagement in consumers with serious mental illness.
CONDITIONS
Official Title
Context-Aware Mobile Intervention for Social Recovery in Serious Mental Illness (R33)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Voluntary informed consent and ability to consent
- Age 18 to 65 years
- Diagnosis of schizophrenia, schizoaffective disorder, bipolar I disorder, or major depression with history of psychosis
- Minimum social avoidance defined by a score of 6 2 on the Scale for the Assessment of Negative Symptoms (SANS) asociality item
- Willing and able to speak and read English at 6th grade level or higher
You will not qualify if you...
- Received cognitive-behavioral therapy in the past 2 years
- Greater than moderate disorganization on the Positive and Negative Syndrome Scale (PANSS) Disorganization item (>5)
- Alcohol or substance dependence in the past 3 months
- Level of care required that interferes with outpatient therapy (e.g., hospitalization, severe medical illness)
- Unable to see or manually use a phone adequately
- Resident of an integrated housing facility that provides treatment services
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of California - San Diego
San Diego, California, United States, 92093
Actively Recruiting
Research Team
J
Jason Holden, PhD
CONTACT
E
Eric Granholm, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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