← Back to Clinical Trials
Recruiting NCT06138054

NCT06138054 MI-CBTech: A Mobile Intervention for Community Integration in Homeless-Experienced Veterans With SMI

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06138054
Status Recruiting
Phase
Sponsor VA Office of Research and Development
Condition Schizophrenia Spectrum Disorders
Study Type INTERVENTIONAL
Enrollment 50 participants
Start Date 2024-04-01
Primary Completion 2026-09-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
MI-CBTechMindfulness control

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 50 participants in total. It began in 2024-04-01 with a primary completion date of 2026-09-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study aims to test the feasibility and acceptability of a brief behavioral intervention that combines two treatments, Motivational Interviewing (MI) and Cognitive Behavioral Therapy (CBT), that have been shown to work in prior research studies. The format of the intervention will be a combination of in-person sessions and remote elements delivered via mobile phone (together called MI-CBTech). The goal of the intervention is to improve community integration in Veterans with serious mental illness (SMI) who have experienced homelessness. A time- and format-matched control arm will include remote mindfulness training. 50 Veterans with SMI experiencing homelessness will be randomized to one of the two arms (25 per arm).

Eligibility Criteria

Inclusion Criteria: * Veterans currently residing at the VA Greater Los Angeles Mental Health Residential Rehabilitation Treatment Program (Domiciliary) * age 18-65 years * diagnosis of non-affective or affective psychotic illness as confirmed by chart review * history of homelessness * sufficiently fluent in English to consent, understand procedures, and complete assessments and intervention * medically and clinically stable (i.e. able to participate in and complete assessments and intervention). Exclusion Criteria: * history of clinically significant neurological disorder determined by medical history (e.g., epilepsy) * history of serious head injury (i.e., loss of consciousness \> 1 hr, neuropsychological sequelae, cognitive rehabilitation post head injury) * evidence of IQ \< 70 or developmental disability * moderate or severe substance use disorder in the past month based on chart review

Contact & Investigator

Central Contact

Amy M Jimenez, PhD

✉ Amy.Jimenez@va.gov

📞 (310) 478-3711

Principal Investigator

Amy M Jimenez, PhD

PRINCIPAL INVESTIGATOR

VA Greater Los Angeles Healthcare System, West Los Angeles, CA

Frequently Asked Questions

Who can join the NCT06138054 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Schizophrenia Spectrum Disorders. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06138054 currently recruiting?

Yes, NCT06138054 is actively recruiting participants. Contact the research team at Amy.Jimenez@va.gov for enrollment information.

Where is the NCT06138054 trial being conducted?

This trial is being conducted at West Los Angeles, United States.

Who is sponsoring the NCT06138054 clinical trial?

NCT06138054 is sponsored by VA Office of Research and Development. The principal investigator is Amy M Jimenez, PhD at VA Greater Los Angeles Healthcare System, West Los Angeles, CA. The trial plans to enroll 50 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology