- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03589521
Adapting Alcohol Behavioral Couple Therapy for Service Members in Post-Deployment (ABCT_Mil)
May 21, 2019 updated by: Elizabeth Epstein, University of Massachusetts, Worcester
The specific aims of the ABCT_Military project are as follows: 1) To modify the existing, Alcohol Behavioral Couple Therapy (ABCT) model to treat service members in the reconstitution (post deployment, reintegration, or separation) stage of service, and develop optional psychoeducation modules to address relevant co-morbid problems and challenges in this population in a weekly, 15 session, stand-alone outpatient format.
2) To test feasibility and preliminary efficacy of the study intervention protocol in a successive cohort design for one cohort of 8 couples and one cohort of 22 couples, with iterative manual revision.
Study Overview
Detailed Description
The study staff will screen potential participants over the phone, and arrange Baseline (BL) research interviews for appropriate couples.
The couple will meet with the program interviewer for approximately 2 hours.
After the BL interview, couples will be scheduled to attend therapy sessions.
Couples will complete brief within treatment self-report assessments.
Couples will complete a post treatment follow up interview four months after session 1.
Study Type
Interventional
Enrollment (Actual)
60
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
-
-
Massachusetts
-
Worcester, Massachusetts, United States, 01655
- University of Massachusetts Medical School
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age 18 and older;
- Married (or separated with efforts to reconcile) or in a committed relationship (cohabiting, or in an exclusive dating relationship), or significant other (SO) (first, second or third degree relative (including step relative or in-law) or close trusted friend not active in same military branch. The service member only must meet the following inclusion criteria:
- Served or serving in the U.S. Military,
- Current Alcohol Use Disorder diagnosis, or drink at high risk levels as defined by NIAAA (2010)
Exclusion Criteria:
- Either individual is not fluent in the English language.
Exclusion criteria for the service member only:
- Unstabilized Psychotic disorder in past six months
Exclusion criteria for both members of the couple if SO is spouse/romantic partner:
- Either partner is fearful of participating in couple therapy OR either partner suffered severe physical abuse from partner when perpetrator not intoxicated, in past year
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: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: ABCT_Military
ABCT_Military manual will address alcohol use, couple issues and military specific issues.
Required interventions include: routine interventions, overview of treatment, reintegration issues, motivational techniques, patient-focused interventions for abstinence, partner-related interventions for abstinence, couple interventions, general coping skills, social skills and relapse prevention.
In addition, to personalize each treatment plan, interventions from optional modules (e.g., intimate partner violence (IPV), depression, trauma, and traumatic brain injury (TBI)) will be integrated into each couple's treatment plan depending on clinical presentation.
|
15 Weekly Couple Therapy Sessions
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percent Drinking Days (PDD)
Time Frame: Change from baseline at 4 months post Session 1
|
Derived from Timeline Followback (TLFB)
|
Change from baseline at 4 months post Session 1
|
|
Percent Heavy Drinking Days
Time Frame: Change from baseline at 4 months post Session 1
|
Derived from Timeline Followback (TLFB)
|
Change from baseline at 4 months post Session 1
|
|
Mean Drinks Per Drinking Day
Time Frame: Change from baseline at 4 months post Session 1
|
Derived from Timeline Followback (TLFB)
|
Change from baseline at 4 months post Session 1
|
|
Couple Satisfaction Inventory 16
Time Frame: Change from baseline at 4 months post Session 1
|
16 item measure assessing satisfaction in couple relationship.
Scores range from 0 to 81 and higher scores indicate higher levels of relationship satisfaction.
Total score is calculated by summing all values.
|
Change from baseline at 4 months post Session 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Coping Strategies Scale
Time Frame: Change from baseline at 4 months post Session 1
|
25-item brief measure assessing coping in alcohol-specific and non-alcohol situations.
Scores range from 1-4 and higher scores indicate greater use of coping skills.
Total score is calculated by averaging all values.
|
Change from baseline at 4 months post Session 1
|
|
World Health Quality of Life Questionnaire - Bref
Time Frame: Change from baseline at 4 months post Session 1
|
26-item self report assessing quality of life across 4 domains/subscales: Physical health, Psychological, Social relationships, Environment.
The first two items measure quality of life and overall health and are examined separately, with scores ranging from 1-5.
The four domain scores are calculated by averaging values and scores range from 1-5.
Higher scores indicate higher quality of life within each domain.
Mean scores are then multiplied by 4 in order to make domain scores comparable with the scores used in the WHOQOL-100 (full scale measure).
|
Change from baseline at 4 months post Session 1
|
|
Treatment Services Review
Time Frame: Weekly during treatment, for up to 16 weeks
|
Interview assessing quantity and type of services received (e.g., health, psychological) outside of study intervention.
Total scores are calculated by summing the number of outside services used.
Total scores have a minimum of 0 and no maximum value.
|
Weekly during treatment, for up to 16 weeks
|
|
Working Alliance Inventory Short Form
Time Frame: Baseline and through study completion, about 16 weeks
|
12-item self-report measure of the therapeutic alliance.
Total scales are calculated by summing all values.
Values range from 1-7 with total scores ranging from 12 to 84).
Higher scores indicate greater alliance.
|
Baseline and through study completion, about 16 weeks
|
|
Post-Traumatic Stress Disorder (PTSD)
Time Frame: Baseline
|
Percent of sample with a PTSD diagnosis as determined by scores on the Life Events Checklist (LEC-5) and the PTSD Checklist (PCL-5).
|
Baseline
|
|
PTSD Checklist (PCL-5)
Time Frame: Baseline and through study completion, about 16 weeks
|
20-item self-report questionnaires assessing current symptoms of PTSD, used to assess current (past 30 days) PTSD severity.
Total scores are calculated by summing all values.
Scores on the PCL-5 range from 0-80 and reflect a global PTSD severity score, with higher scores indicating greater severity.
|
Baseline and through study completion, about 16 weeks
|
|
Use of Treatment Skills
Time Frame: Baseline and through study completion, about 16 weeks
|
Self-report questionnaire assessing use of skills learned during treatment.
Item scores range from 1-5 and a total score is calculated by summing all values.
Higher scores indicate greater use of skills.
|
Baseline and through study completion, about 16 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Traumatic Brain Injury (TBI)
Time Frame: Baseline
|
Percent of sample with a TBI as determined by scores on the TBI Checklist.
|
Baseline
|
|
Traumatic Brain Injury (TBI) Checklist
Time Frame: Change from baseline at 4 months post Session 1
|
Severity of TBI as determined by total scores on the TBI Checklist.
Scores are calculated by summing individual item scores with possible scores ranging from 8 to 88.
|
Change from baseline at 4 months post Session 1
|
|
Beck Depression Inventory II (BDI-II)
Time Frame: Change from baseline at 4 months post Session 1
|
self-report questionnaire assessing depression symptoms over the prior two weeks (scores range 0-63) and higher scores indicate greater depression symptomatology.
All item scores are summed to attain a total score.
|
Change from baseline at 4 months post Session 1
|
|
Copello Coping Questionnaire
Time Frame: Change from baseline at 4 months post Session 1
|
30 item self-report assessing partner alcohol-related coping skill use.
Total score is calculated by summing the values from each item and scores range from 0-90 with higher scored indicating greater use of coping strategies.
|
Change from baseline at 4 months post Session 1
|
|
Intimate Partner Violence (IPV)
Time Frame: Change from baseline at 4 months post Session 1
|
Percent of sample with IPV as determined by scores on the Conflict Screener Form H.
|
Change from baseline at 4 months post Session 1
|
|
Stages of Change Readiness and Treatment Eagerness Scale (SOCRATES) Short Form
Time Frame: Change from baseline at 4 months post Session 1
|
19 item self-report questionnaire assessing client readiness for change.
An additional item assesses the client's motivation for coming to therapy.
There are three sub scales (Recognition, Ambivalence, and Taking Steps) which are derived from individual items.
Higher scores indicate greater recognition, ambivalence and taking steps and scores range from 7 to 35, 4 to 20, and 8-40, respectively.
|
Change from baseline at 4 months post Session 1
|
|
Partner Quantity Frequency Questionnaire
Time Frame: Change from baseline at 4 months post Session 1
|
Self-report questionnaire assessing frequency and quantity of current and lifetime substance use.
Measure is used to provide descriptive data about partner substance use.
Total scores are not used.
|
Change from baseline at 4 months post Session 1
|
|
Medical History Questionnaire
Time Frame: Change from baseline at 4 months post Session 1
|
40 item self-report assessing presence of medical conditions currently and in the past.
Scores are calculated by summing individual item scores with possible scores ranging from 0 to 40.
Higher scores indicate greater number of medical problems.
|
Change from baseline at 4 months post Session 1
|
|
End of Treatment Questionnaire
Time Frame: 4 months post session 1
|
Self-report questionnaire of helpfulness of therapy elements on a 7 point scale of -3 (greatly harmful), -2, -1, 0 (neutral), +1, +2, +3 (greatly helpful).
Total scores are calculated by averaging scores across individual items.
|
4 months post session 1
|
|
Brief COPE
Time Frame: Change from baseline at 4 months post Session 1
|
28 item self-report assessing general coping skill use.
Sub scale scores are calculated by summing individual items (2 items per sub scale) with possible scores of 2 to 8. The sub scales are: Self-distraction, Active coping, Denial, Substance use, Use of emotional support, Use of instrumental support, Behavioral disengagement, Venting, Positive reframing, Planning, Humor, Acceptance, Religion, and Self-blame.
Higher scores reflect greater use of each category of coping skills.
|
Change from baseline at 4 months post Session 1
|
|
Client Satisfaction Questionnaire
Time Frame: 4 months post session 1
|
8 item self-report assessing satisfaction with treatment.
Individual item scores are averaged to calculate a total score with possible scores ranging from 0 to 4. Two additional items assessed the client's ideal number of sessions and length of treatment, with scores ranging from 1 to 24 sessions and 1-12 months.
|
4 months post session 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
June 1, 2015
Primary Completion (Actual)
November 28, 2018
Study Completion (Actual)
November 28, 2018
Study Registration Dates
First Submitted
June 8, 2018
First Submitted That Met QC Criteria
July 4, 2018
First Posted (Actual)
July 18, 2018
Study Record Updates
Last Update Posted (Actual)
May 23, 2019
Last Update Submitted That Met QC Criteria
May 21, 2019
Last Verified
May 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AA023027
- 5R34AA023027 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual Participant Data will not be shared with investigators outside of the core study team.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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