Skip to content

Behavioral Treatment for Substance Abuse

A Pilot Study of Two Group-based Intervention Programs for Patients With Substance Abuse Problems

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01438346
Enrollment
38
Registered
2011-09-22
Start date
2011-08-31
Completion date
2012-08-31
Last updated
2016-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Substance-Related Disorders

Keywords

Substance Abuse, Substance Addiction, Substance Dependence, Treatment program

Brief summary

This pilot project will evaluate a new mind-body intervention called Mind-Body Bridging (MBB) for reducing substance abuse problems in women who are undergoing a substance abuse treatment program. The main hypothesis is that MBB will be more effective than the control (standard) intervention program in helping people reduce their craving for illicit substances and/or alcohol.

Detailed description

This is a randomized clinical pilot study in which MBB will be compared with a standard treatment program for substance abuse. Both groups will run concurrently over the course of a 10-week period, twice per week.

Interventions

BEHAVIORALSubstance Abuse Education

10 weeks of usual care for substance abuse.

Two sessions per week for 10 weeks, besides usual care treatment for substance abuse.

Sponsors

University of Utah
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Substance abuse or dependence * Resident/day client in the House of Hope substance abuse treatment program * Minimum stay in treatment at House of Hope for 3.5 months * Fluent in English

Exclusion criteria

* Psychosis * Suicide risk * Dementia * Significant withdrawal risk * Severe, unstable depression * Requires intensive mental health treatment * Cognitive impairment

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in the measure of the Penn Alcohol and Craving ScaleWeek 5 and Week 11Change from baseline in the extent of drug and alcohol craving at Week 5 and Week 11, as measured by a modified version of the Penn Alcohol and Craving Scale
Change from baseline in Alcohol and Drug Use Consequences ScaleWeek 5 and Week 11Change from baseline in the measure of alcohol and drug consequences at Week 5 and Week 11, as measured by Alcohol and Drug Use Consequences Scale

Secondary

MeasureTime frameDescription
SleepPre (Baseline) Mid (Week 5), Post (Week 11)The Medical Outcomes Study Sleep Scale (MOS-SS) provides an index of sleep problems and incorporates six sleep scale scores: 1) sleep disturbance, 2) sleep adequacy, 3) daytime somnolence, 4) snoring, 5) waking up short of breath with a headache, and 6) quantity of sleep. The MOS-SS is similar to the Pittsburgh Sleep Quality Index (PSQI) developed at the same time, which includes more questions about sleep disturbance with seven more items overall. The 1-week assessment is adapted from the normal 4-week retrospective assessment.
MindfulnessPre (Baseline) Mid (Week 5), Post (Week 11)The Five-facet Mindfulness Questionnaire (FFMQ) comprises five clear, interpretable facets of mindfulness: acting with awareness, observing, describing, non-judging, non-reacting.
Subjective distressPre (Baseline) Mid (Week 5), Post (Week 11)Impact of Events Scale - Revised (IES-R) is a 22-item self-report measure that assesses subjective distress caused by traumatic events. The IES-R yields a total score (ranging from 0 to 88) and subscale scores can also be calculated for the Intrusion, Avoidance, and Hyperarousal subscales.
Well-beingWeekly for 11 weeksThe Well-Being Index (WBI)is a 5-item scale developed and validated by the World Health Organization Collaborating Centre in Mental Health. The WBI will be used to assess whether participants show any changes in general well-being.
Self-CompassionPre (Baseline) Mid (Week 5), Post (Week 11)Self compassion is measured by the Self-Compassion Scale that comprises 26 items. Self-compassion is an emotionally positive self-attitude that should protect against the negative consequences of self-judgment, isolation, and rumination (such as depression).
DepressionPre (Baseline) Mid (Week 5), Post (Week 11)The Center for Epidemiologic Studies Depression Scale is one of the most common screening tests to determine an individual's depression quotient. The test measures depressive feelings and behaviors during the past week.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026