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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01886716
Other study ID # 1R21AA021151
Secondary ID 1R21AA021151
Status Completed
Phase N/A
First received June 17, 2013
Last updated December 15, 2014
Start date July 2013
Est. completion date December 2014

Study information

Verified date December 2014
Source University of Cincinnati
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review BoardUnited States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this research is to test a computerized intervention for people with co-occurring social anxiety and alcohol dependence. The intervention seeks to reduce symptoms by shifting attention away from alcohol-relevant and/or socially threatening cues. The investigators expect that participants receiving alcohol or anxiety training will experience reductions in those specific symptoms compared to participants in a control condition. The investigators also expect that participants receiving combined alcohol and anxiety training will show the largest reductions in alcohol and anxiety symptoms, relative to participants in any other condition.


Recruitment information / eligibility

Status Completed
Enrollment 115
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Current alcohol dependence

- Elevated social anxiety symptoms

- Willingness to consider cutting down on drinking

Exclusion Criteria:

- Current psychosis

- Unmanaged manic symptoms

- Significant cognitive impairment

- Other drug use in past month

- Receiving cognitive behavioral therapy for alcohol use disorder or social anxiety

- Unable to read

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Anxiety Attention Training
Anxiety Attention Training will preferentially direct participants' attention away from reminders of anxiety.
Alcohol Attention Training
Alcohol Attention Training will preferentially direct participants' attention away from reminders of alcohol.

Locations

Country Name City State
United States University of Cincinnati Department of Family and Community Medicine Cincinnati Ohio

Sponsors (4)

Lead Sponsor Collaborator
University of Cincinnati Brown University, National Institute on Alcohol Abuse and Alcoholism (NIAAA), University of Miami

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Liebowitz Social Anxiety Scale End of Training (4 weeks) No
Primary 30-Day Timeline Follow-back for Alcohol and Drugs End of Training (4 weeks) No
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