Purpose

Almost 18 million US adults have alcohol use disorders (AUD), with one third of these individuals also diagnosed with anxiety disorders (AXD). The coexistence of AUD and AXD imposes a high burden via healthcare costs and lost productivity. To date, existing treatment approaches for addressing AUD/AXD comorbidity have been only modestly effective and there is a lack of adequate research to guide treatment decisions. The Unified Protocol (UP) is a transdiagnostic, cognitive-behavioral therapy that has shown efficacy in treating emotional disorders. The efficacy of the UP to facilitate abstinence from alcohol consumption in individuals with comorbid AUD/AXD has also been examined, with results from this study indicating a reduction from baseline in drinks consumed per day. However, further evaluation of the UP for managing AUD/AXD is warranted. In this clinical trial, the investigators will further assess the UP's effectiveness in reducing alcohol consumption in patients with comorbid AUD/AXD. Participants will be randomized to one of two conditions: 1) treatment with the UP or 2) treatment with therapist-guided Take Control (TC; a computerized alcohol reduction program). In addition, in a subset of twenty-five participants, functional magnetic resonance scanning (fMRI) will be used to examine the effects of the UP on changes in brain activity in areas important to regulation of emotional and reward processes implicated in excessive alcohol consumption. The researchers' primary hypotheses are that the UP group will, compared to the TC group: 1) be superior in acute symptom reduction from pre- to post-treatment, and 2) evidence greater reductions in percent days heavy drinking, percent days of drinking per week, and alcohol craving.

Conditions

Eligibility

Eligible Ages
Over 21 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Criteria

1. DSM-5 diagnosis of an alcohol use disorder (AUD)

2. DSM-5 diagnosis of Social Anxiety Disorder (SAD), Panic Disorder/Agoraphobia (PD/A),
Generalized Anxiety Disorder (GAD), and/or Obsessive Compulsive Disorder (OCD) as
determined by a clinician-administered diagnostic assessment using the Anxiety
Disorder Interview Schedule for DSM-5 (ADIS-5); and are rated as crossing the
threshold for a formal DSM-5 diagnosis by assignment of an ADIS clinical severity
rating (CSR) of 4 (definitely disturbing/disabling on the 0-8 CSR scale) or higher
on at least the principal diagnosis.

3. Adults 21 years old or older

4. Expressed desire to stop drinking alcohol completely or to reduce alcohol
consumption

5. Reported drinking an average of at least 15 standard drinks per week for males, or 8
for females occurring over a 28-consecutive day period during the 90 day-long time
window that preceded the screening session

6. Must be willing to discontinue any form of psychotherapy, except AA, that he or she
may be receiving for either anxiety or depression prior to screening.

Exclusion Criteria:

1. DSM-5 diagnosis of current major depressive disorder (with the exception of
substance-induced depressive disorder) that requires immediate treatment with
pharmacologic agents, bipolar disorder, schizophrenia, current bulimia/anorexia,
dementia, or other substance dependence, with the exception of nicotine, marijuana,
and caffeine dependence.

2. Presence of suicidal ideation or history of suicide attempts

3. Non-English speakers

4. Previously received an adequate trial of cognitive-behavioral therapy (CBT; 8
sessions within the past 5 years)

5. Contraindications to MRI scans

6. History of head injury with >5-minute loss of consciousness

7. Pregnancy Note: Women of childbearing potential (not postmenopausal for at least one
year) will be required to provide a negative urine pregnancy test prior to each
scan.

8. Implantation of anything containing magnetically sensitive material including metal
plates, aneurysm clips, and cardiac pacemakers, stents; history of sheet metal work,
claustrophobia

9. Cognitive impairment (MOCA<21).

10. Serious medical illness or instability for which hospitalization may be likely
within the next year.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Intervention Model Description
Participants will be randomized to one of two conditions: 1) treatment with the UP or 2) treatment with therapist-guided Take Control (TC; a computerized alcohol reduction program). In addition, in a subset of twenty-five participants, functional magnetic resonance scanning (fMRI) will be used to examine the effects of the UP on changes in brain activity in areas important to regulation of emotional and reward processes implicated in excessive alcohol consumption.
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
Active Comparator
Unified Protocol
The Unified Protocol for Transdiagnostic Treatment of Emotional Disorders (UP) consists of 5 core skills modules based on cognitive behavioral treatment elements of proven effectiveness. As noted above, these core skills modules were designed to target (and have been shown to address) negative emotionality and aversive reactivity to emotional experiences when they occur (Boswell et al., 2013; Carl et al., 2014; Sauer-Zavala et al., 2012). These modules are preceded by an introductory session that reviews the patient's presenting symptoms and provides a therapeutic rationale, as well as a module on motivational enhancement. A final module consists of relapse prevention. As the treatment proceeds, the domains of thoughts, feelings, and behaviors are each explored in detail, focusing specifically on elucidating dysfunctional emotion regulation strategies that the patient has developed over time within each of these domains, and teaching patients more adaptive emotion regulation skills.
  • Behavioral: Unified Protocol for Transdiagnostic Treatment of Emotional Disorders
    The UP will be conducted in a standardized fashion, over 16 sessions, following the published therapist guide with minor refinements for application in the proposed comorbid population.
    Other names:
    • UP
Placebo Comparator
Take Control
TC is a psychotherapy platform derived from the National Institute on Alcohol Abuse and Alcoholism's (NIAAA) self-help approach, Rethinking Drinking. In this study, TC, originally designed as a computerized treatment has been modified to be administered by the therapist to control for effects that may be related to patient-therapist interaction (as opposed to elements of the treatment itself). Specifically, on a weekly basis, therapists will review material from TC and offer general advice on implementation of the alcohol reduction skills in daily life.
  • Behavioral: Take Control
    TC is a psychotherapy platform derived from the National Institute on Alcohol Abuse and Alcoholism's (NIAAA) self-help approach, Rethinking Drinking. In this study, TC, originally designed as a computerized treatment has been modified to be administered by the therapist to control for effects that may be related to patient-therapist interaction (as opposed to elements of the treatment itself). Specifically, on a weekly basis, therapists will review material from TC and offer general advice on implementation of the alcohol reduction skills in daily life.
    Other names:
    • TC

Recruiting Locations

More Details

Status
Recruiting
Sponsor
Boston University Charles River Campus

Study Contact

Todd Farchione, PhD
617-353-9610
tfarchio@bu.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.