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Intervention for Persons Leaving Residential Substance Abuse Treatment

Not Applicable
Completed
Conditions
Substance Use Disorders
Interventions
Behavioral: Critical Time Intervention-Residential (CTI-R)
Behavioral: Enhanced Usual Discharge Services-Residential
Registration Number
NCT02670902
Lead Sponsor
New York University
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
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:

    1. Anyone under the age of 18
    2. Non-English speaking individuals due to limited resources
    3. Individuals who are considered vulnerable/protected populations, including children, pregnant women, and prisoners.
    4. Individuals judged by clinical treatment staff to be in immediate crisis, i.e., suicide watch or inadequate decisional capacity to participate in the study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Critical Time Intervention-ResidentialCritical Time Intervention-Residential (CTI-R)CTI-R is a 9-month, assertive outreach and linkage program.
Critical Time Intervention-ResidentialEnhanced Usual Discharge Services-ResidentialCTI-R is a 9-month, assertive outreach and linkage program.
Enhanced Usual Discharge-ResidentialEnhanced Usual Discharge Services-ResidentialThe enhanced usual discharge condition includes usual discharge services plus enhanced transition services.
Primary Outcome Measures
NameTimeMethod
EnrollmentBaseline

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

Change in retention3, 6, 9, and 12 months

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

Short-term Relapse3 months

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

Housing3 months

Proportion of participants housed at the time of discharge

Use of aftercare services3 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 Outcome Measures
NameTimeMethod
Short-term Social Support3 months

Level of social support as measured by the 8-item modified Medical Outcomes Study Social Support Survey

Change in Relapse3, 6, and 9 months

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

Long-term Social Support12 months

Level of social support as measured by the 8-item modified Medical Outcomes Study Social Support Survey

Long-term Self-Efficacy12 months

Level of self-efficacy as measured by "I feel like I'm in control of my alcohol or drug use."

Short-term Self-Efficacy3 months

Level of self-efficacy as measured by "I feel like I'm in control of my alcohol or drug use."

Change in Social Support3, 6, and 9 months

Level of social support as measured by the 8-item modified Medical Outcomes Study Social Support Survey

Change in Mental Health3, 6, and 9 months

Level of mental health severity as measured by the Brief Symptom Inventory

Short-term Mental Health3 months

Level of mental health severity as measured by the Brief Symptom Inventory

Change in Self-Efficacy3, 6, and 9 months

Level of self-efficacy as measured by "I feel like I'm in control of my alcohol or drug use."

Long-term Relapse12 months

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

Long-term Mental Health12 months

Level of mental health severity as measured by the Brief Symptom Inventory

Trial Locations

Locations (1)

New York University

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New York, New York, United States

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