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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01694082
Other study ID # 1207010596
Secondary ID K01AA019694
Status Completed
Phase N/A
First received September 20, 2012
Last updated June 12, 2014
Start date October 2012
Est. completion date June 2014

Study information

Verified date June 2014
Source Yale University
Contact n/a
Is FDA regulated No
Health authority United States: Yale University Human Investigation Committee
Study type Interventional

Clinical Trial Summary

Tertiary Health Research Intervention Via Email (THRIVE; Kypri et al., 2009), originally utilized with Australian students, is unique in that it contains efficacious components derived from motivational interviewing (e.g., personalized feedback) and cognitive behavioral therapy (protective behavioral strategies), yet is very brief and has established efficacy. This study aims to test versions of THRIVE tailored to American college students. In addition to replicating original results with THRIVE, we will also test versions containing unique subsets of protective behavioral strategies to reduce alcohol consumption. The primary hypothesis is that versions of THRIVE will be associated with lower overall alcohol consumption than an assessment and brief brochure control condition.


Recruitment information / eligibility

Status Completed
Enrollment 207
Est. completion date June 2014
Est. primary completion date November 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 24 Years
Eligibility Inclusion Criteria:

- Must be a current student at Albertus Magnus College in New Haven, CT

Exclusion Criteria:

- Under 18 years of age

- 25 years of age or older

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
THRIVE
THRIVE stands for (Tertiary Health Research Intervention Via Email). Participants complete questions related to demographics and their alcohol use and receive brief personalized feedback based on this information, in addition to protective behavioral strategies, facts about alcohol and information about available resources to reduce their alcohol use.
Brief brochure and assessment control


Locations

Country Name City State
United States Yale University School of Medicine New Haven Connecticut

Sponsors (3)

Lead Sponsor Collaborator
Yale University Alcoholic Beverage Medical Research Foundation, National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Frequency of alcohol use 1-month post-intervention No
Primary Protective behavioral strategy use 1-month post-intervention No
Primary Overall Weekly Alcohol Consumption 1-month post-intervention No
Secondary Frequency of heavy drinking days 1-month post-intervention No
Secondary Frequency of alcohol use 6-months post-intervention No
Secondary Overall weekly alcohol consumption 6-months post-intervention No
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