Purpose

This trial aims to evaluate the effectiveness of a novel intervention for Veterans with co-occurring bipolar and substance use disorders following a psychiatric hospitalization. Half of the participants will receive a specialized psychosocial intervention program, while the other half will receive an enhanced safety monitoring program, both provided in addition to their routine care.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Diagnosis of a mood disorder - Diagnosis of a substance use disorder (drug and/or alcohol) - Taking at least one psychiatric medication

Exclusion Criteria

  • Unable to speak and read English - Younger than age 18

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Integrated Treatment Adherence Program for Veterans (ITAP-VA)
A combination of in-person and phone sessions along with significant other involvement over 6 months post-hospitalization.
  • Behavioral: Integrated Treatment Adherence Program for Veterans (ITAP-VA)
    Psychosocial support and treatment to improve treatment adherence, symptoms, and functioning.
Active Comparator
Safety Assessment and Follow-up Evaluation (SAFE)
Enhanced symptom monitoring and safety evaluation over 6 months post-hospitalization.
  • Behavioral: Safety Assessment and Follow-up Evaluation (SAFE)
    Measurement-based care assessment and evaluation.

Recruiting Locations

More Details

Status
Recruiting
Sponsor
VA Office of Research and Development

Study Contact

Jane Metrik, PhD
(401) 273-7100
Jane.Metrik@va.gov

Detailed Description

This randomized controlled trial will evaluate the effectiveness of a psychosocial intervention designed to improve treatment adherence in Veterans with comorbid bipolar disorder and substance use disorders (BP-SUD) following a psychiatric hospitalization. Participants will be randomized to either the specialized psychosocial intervention or an enhanced safety monitoring program, both as adjuncts to VA treatment as usual. Veterans with BP-SUD will be recruited from the Providence VAMC inpatient psychiatric unit and assessed at baseline and at 3 (mid-treatment), 6 (post-treatment), and 9-month post-discharge.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.