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Clinical Trials/NCT02670902
NCT02670902
Completed
N/A

Intervention for Persons With Co-Occurring Disorders Leaving Residential Tx

New York University1 site in 1 country60 target enrollmentMay 1, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Substance Use Disorders
Sponsor
New York University
Enrollment
60
Locations
1
Primary Endpoint
Enrollment
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This research uses a multi-phase approach to adapt and implement an established intervention, Critical Time Intervention, for a new population and setting among individuals with substance use who are at risk of relapse following residential substance abuse treatment. The goals of the study are to: (PHASE 1) identify challenges and strategies of community reentry among individuals in residential substance abuse treatment and their providers and social support networks (e.g., family, friends, community members); (PHASE 2) adapt CTI for individuals in residential substance abuse treatment to prepare them for discharge and transition back into the community; and (PHASE 3) conduct a pilot study to examine the feasibility, acceptability, and preliminary outcomes of the adapted CTI compared to enhanced usual discharge planning services.

Detailed Description

This randomized pilot study will examine the feasibility, acceptability, and preliminary outcomes of the adapted CTI compared to enhanced usual discharge planning services. More specifically, 60 participants will be randomized to either CTI (n=30) or enhanced usual discharge planning services (n=30) at the time of discharge. Participants will complete a baseline interview (prior to randomization) and 3-, 6-, 9- and 12-month follow-up assessments post-discharge.

Registry
clinicaltrials.gov
Start Date
May 1, 2017
End Date
December 31, 2020
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Eligible participants will be enrolled in residential substance abuse treatment and who are at least 18 years of age, speak English, and expect to be discharged within 3 months.

Exclusion Criteria

  • Individuals that do not meet the aforementioned inclusion criteria will be excluded from the study.More specifically, the following categories will be excluded:
  • Anyone under the age of 18
  • Non-English speaking individuals due to limited resources
  • Individuals who are considered vulnerable/protected populations, including children, pregnant women, and prisoners.
  • Individuals judged by clinical treatment staff to be in immediate crisis, i.e., suicide watch or inadequate decisional capacity to participate in the study.

Outcomes

Primary Outcomes

Enrollment

Time Frame: Baseline

Proportion of participants enrolled in the study as measured by the research records

Change in retention

Time Frame: 3, 6, 9, and 12 months

Proportion of participants completed the study as measured by the research records

Short-term Relapse

Time Frame: 3 months

Proportion of participants who relapsed (i.e., substance use) as measured by Addiction Severity Index

Housing

Time Frame: 3 months

Proportion of participants housed at the time of discharge

Use of aftercare services

Time Frame: 3 months

Proportion of participants who were linked to aftercare services (i.e. substance use treatment) at the time of discharge as measured by the Treatment Service Review (TSR)

Secondary Outcomes

  • Short-term Social Support(3 months)
  • Change in Relapse(3, 6, and 9 months)
  • Long-term Social Support(12 months)
  • Long-term Self-Efficacy(12 months)
  • Short-term Self-Efficacy(3 months)
  • Change in Social Support(3, 6, and 9 months)
  • Change in Mental Health(3, 6, and 9 months)
  • Short-term Mental Health(3 months)
  • Change in Self-Efficacy(3, 6, and 9 months)
  • Long-term Relapse(12 months)
  • Long-term Mental Health(12 months)

Study Sites (1)

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