- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03329157
Rebuilding Bridges for Homeless Veterans
January 17, 2025 updated by: VA Connecticut Healthcare System
Pilot study on an intervention called Rebuilding Bridges to help veterans re-engaged with loved ones.
Study Overview
Detailed Description
The objective of the proposed project is to examine the feasibility and acceptability of the Rebuilding Bridges intervention, which was designed to help homeless Veterans plan and implement steps to engage friends, family and other loved ones in their lives.
The PI and his team will enroll approximately 25-30 Veterans.
Veterans will be recruited via provider referral and via advertisements that will be placed in general clinical areas and desks at the Errera Center.
The PI will work with the Veterans to create a detailed genogram of family, friends and other supporters in the Veteran's life.
This will be followed by a meeting with each Veteran over the course of three 30-minute weekly sessions to help the Veteran identify and engage people listed in their genogram which the Veteran might want to form stronger relationships with.
Veterans will also be asked to complete several measures and questionnaires such as housing information, employment, mental health and quality of life.
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Connecticut
-
West Haven, Connecticut, United States, 06516
- VA Connecticut Healthcare System
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria
- Over 18 years old
- Currently in a VA homeless program
- Able to provide valid consent
Exclusion Criteria
- Acute psychiatric decompensation requiring inpatient admission or emergency department services within the last month (suicidality, homicidally, mania, psychotic decompensation)
- Has a conservator
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Rebuilding Bridges
This is a one-group study and the group will receive the Rebuilding Bridges intervention
|
Psychosocial intervention to help veterans re-engage with family members called Rebuilding Bridges, developed for this project.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social Support
Time Frame: 2 years
|
2-Way Social Support scale and the Multidimensional Scale of Perceived Social Support, which generates a total score from 1 to 7 with higher scores indicating greater social support
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Housing status
Time Frame: 2 years
|
Nights stayed in own place and nights homeless in the past 60 days, which should total 60 days.
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jack Tsai, PhD, VA Connecticut
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2023
Primary Completion (Actual)
November 10, 2024
Study Completion (Actual)
November 10, 2024
Study Registration Dates
First Submitted
October 23, 2017
First Submitted That Met QC Criteria
October 30, 2017
First Posted (Actual)
November 1, 2017
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 17, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 102317
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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