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Clinical Trials/NCT00846638
NCT00846638
Completed
Phase 3

Screening and Brief Intervention for Problem Drinking Women

Brigham and Women's Hospital1 site in 1 country611 target enrollmentJanuary 2005

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Risk Drinking,Diabetes, Hypertension, Osteoporosis, Infertility
Sponsor
Brigham and Women's Hospital
Enrollment
611
Locations
1
Primary Endpoint
Drinking outcome
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

The purpose of this randomized trial is to test the effectiveness of screening and brief intervention for risk drinking by nonpregnant women with specific medical problems exacerbated by excessive alcohol consumption. The medical problems are female factor infertility, hypertension, diabetes, and osteoporosis, conditions that are costly to treat and difficult to manage. Just as pregnant women are thought to be highly motivated to modify their alcohol consumption, so women with specific medical problems worsened by alcohol intake are an appropriate group to receive a brief intervention.

Registry
clinicaltrials.gov
Start Date
January 2005
End Date
May 2009
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • has diabetes, hypertension, osteoporosis, or infertility
  • Not currently receiving treatment for alcohol or drug problems or substance related medical illness
  • Not currently experiencing physical dependence on alcohol, requiring medically supervised detoxification
  • Not currently abusing or physically dependent on opiates, cocaine, or other illicit drugs
  • Not currently pregnant. Subjects with infertility may become pregnant during the course of the study.
  • Not currently nursing.
  • Able to complete study measures.

Exclusion Criteria

  • Alcohol screen negative or drinks within NIAAA sensible drinking limits for women
  • Does not agree to randomization and study terms

Outcomes

Primary Outcomes

Drinking outcome

Time Frame: 12 months post enrollment

Study Sites (1)

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