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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03589274
Other study ID # 03-346R08x
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2010
Est. completion date April 28, 2014

Study information

Verified date July 2018
Source Rutgers, The State University of New Jersey
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study has 4 specific aims: (1) To modify our existing Individual Female Specific Cognitive Behavioral Therapy (I-FS-CBT) for Alcohol Use Disorder (AUD) approach to treat women with alcohol dependence in a group format, Group Female Specific Cognitive Behavioral Therapy (G-FS-CBT); (2) To test the relative efficacy of I-FS-CBT and G-FS-CBT; (3) To test hypothesized mechanisms of change in drinking that are common to both treatments, including (a) coping skills and enhanced self-efficacy for abstinence; (b) enhanced sense of autonomy; (c) alleviation of negative affect, and (d) increased social network support for abstinence, and (4) To assess the relative cost-effectiveness of the individual and group treatment.


Description:

Participants completed a telephone screen for initial eligibility and were scheduled for an in-person clinical intake interview. Consented women were scheduled for a baseline research interview (BL) approximately one week later. At the end of the BL, participants were randomized to treatment condition. During the 12 session treatment period, women completed assessments at the beginning and end of each therapy session on secondary outcome and therapy process variables.

In I-FS-CBT each participant saw a therapist weekly. The first session was 90 minutes long, and subsequent sessions were 60 minutes long. The I-FS-CBT manual included core CBT, motivational enhancement, and relapse prevention components. Two core thematic women's issues were integrated into each session via discussion and illustrative material: (a) self-confidence and (b) self-care.

The G-FS-CBT manual included material identical to I-FS-CBT, but the session organization was modified for a closed group format. The group treatment was designed to provide didactic presentation of coping skills and motivational enhancement material, and group discussion and rehearsal of new skills within a supportive atmosphere that facilitated mutual emotional support and support for abstinence. The first session of G-FS-CBT was 2 hours; remaining sessions were 90 minutes.

In-person follow-up interviews were done at 3, 9, and 15 months post-session 1.


Recruitment information / eligibility

Status Completed
Enrollment 155
Est. completion date April 28, 2014
Est. primary completion date April 28, 2014
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age 18 or older

- have a current (past year) Diagnostic and Statistical Manual-IV (DSM-IV) alcohol dependence diagnosis

- used alcohol in the 60 days prior to telephone screening

Exclusion Criteria:

- have psychotic symptoms in the past six months

- gross cognitive impairment

- current physiological dependence on any illicit drug

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
I-FS-CBT
12 manual-guided sessions of I-FS-CBT
G-FS-CBT
12 manual-guided sessions of G-FS-CBT

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Rutgers, The State University of New Jersey

Outcome

Type Measure Description Time frame Safety issue
Other End of Treatment Questionnaire Measured client ratings of helpfulness of therapy elements on a 7 point scale of -3 (greatly harmful), -2, -1, 0 (neutral), +1, +2, +3 (greatly helpful). 3 months post session 1
Other Working Alliance Inventory - Short Form 12-item self-report measure of the therapeutic alliance (7-point scale with a total possible score of 84) Weekly during Treatment, about 15 weeks
Other Therapy Integrity Rating Scale 39 five-point Likert scale items to assess domains common to both treatment conditions (e.g., general interventions, female-specific interventions, common factors) and unique to a single treatment condition (e.g., group therapy interventions) Weekly during treatment, about 15 weeks
Other Therapist Checklist Coding treatment components delivered in each session from 3 to 0 as thoroughly, moderately, minimally, or not covered Weekly during Treatment, about 15 weeks
Primary Percent Drinking Days (PDD) Derived from Timeline Followback (TLFB) Change from baseline across 15 months post-session 1
Primary Percent Heavy Drinking Days (PHDD) Derived from TLFB; Defined as 4 or more standard drinks per day Change from baseline across 15 months post-session 1
Primary Mean Drinks Per Drinking Day (MDPDD) Derived from TLFB Change from baseline across 15 months post-session 1
Secondary Beck Depression Inventory II 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. Baseline and through study completion, about 15 months
Secondary Anxiety Assessed anxiety symptoms in the last week (scores range 0-63) with higher scores indicating higher anxiety symptomatology. Item scores summed to attain total score. Baseline and through study completion, about 15 months
Secondary Sociotropy-Autonomy Scale Measures the extent of an individual's concern with others' opinion of herself (sociotropy) and self-confidence, behavioral and emotional independence (autonomy). Sociotropy sub scale ranges from 0 to 64 with higher scores indicating higher sociotropy. Average Sociotropy Scores are attained by averaging items, with total scores from 0 to 4. Autonomy sub scale Score range from 0 to 44 with higher scores indicating greater autonomy. Average Autonomy Scores are attained by averaging items, with total scores from 0 to 4. Baseline and through study completion, about 15 months
Secondary Coping Strategies Scale Assessed use frequency of 30 strategies to cope with alcohol use and non-alcohol related situations, on a scale of 1 (never) to 4 (frequently) for a mean score across all items Baseline and through study completion, about 15 months
Secondary Situational Confidence Scale 8 Measured self-efficacy to abstain from alcohol use in high-risk situations; each item is rated 0% to 100% for a global confidence score. Baseline and through study completion, about 15 months
Secondary Important People Inventory Assessed social network structure, network drinking, and network response to drinking and abstinence. Percentage of network accepting/encouraging abstinence and percentage of network abstainers/in recovery were used. Baseline and through study completion, about 15 months
Secondary Self care Assessed 8 domains of self-care: seek medical care, have free time, pleasurable activities, social contact, attend treatment, exercise, do nice things for oneself, buy nice things for oneself Baseline and through study completion, about 15 months
Secondary Inventory of Personal Problems Assessed problems in 10 interpersonal domains, rated on a 0 to 4 scale. A total sum score was used for this study; higher scores reflect more interpersonal problems Baseline and through study completion, about 15 months
Secondary Group Environment Scale Form R Measured 10 group process subscales (e.g., Cohesiveness, Leader Support, Order/Organization, Expressiveness, Anger/Aggression), each with a mean scale score for 4 items rated on a 0-4 scale. Baseline and through study completion, about 15 months
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