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Preventing Alcohol Misuse and Consequences in Vulnerable Women

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Lifespan

Status

Unknown

Conditions

Alcohol Drinking

Treatments

Behavioral: Behavioral: Motivational Interview (MI)
Behavioral: Behavioral: Health Coaching (HC)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05010187
K23AA028513 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Heavy alcohol use is a pressing public health issue that results in more negative consequences for young adult women, despite them drinking at lower rates than their male peers. However, particular groups of women, such as women who identify as lesbian and bisexual (i.e., sexual minority women), evidence markedly higher rates of alcohol misuse as well as negative consequences from this use. Sexual minority women are more likely to use alcohol, do so at problematic levels, and to meet criteria for alcohol use disorders than heterosexual women and sexual minority men. Despite these disparities, as well as evidence that sexual minority women have unique mechanisms of risk (e.g., minority stress, social context), there are currently no interventions designed to reduce alcohol misuse among sexual minority women. This study represents the first attempt to design an in-person intervention specifically tailored to sexual minority women, which will be accomplished through an Intervention Mapping framework to identify behavioral determinants of their use (e.g., minority stress and distress; social context) and then map effective behavior change strategies onto these determinants.

Full description

This particular study aim is devoted to the piloting of a brief motivational intervention to reduce alcohol misuse and consequences among sexual minority women. The objective of this study aim is to examine the preliminary feasibility and acceptability of the intervention following treatment development and refinement. Participants will be randomized to a brief intervention or an attention-matched control arm. Participants in both conditions will complete: a baseline survey as well as a follow-up assessment at 1- and 4-months post-intervention. The investigators hypothesize that the developed intervention will be feasible (as indicated by the number of women eligible who consent, attend their intervention session, and return for follow up). The investigators also hypothesize that the intervention will be acceptable to sexual minority women. The investigators will also obtain preliminary evidence of intervention efficacy in terms of alcohol use outcomes. Specifically, the investigators hypothesize that participants in the intervention will report less frequent heavy episodic drinking and fewer alcohol consequences post-intervention compared with those in the control group.

Enrollment

70 estimated patients

Sex

Female

Ages

18 to 29 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Female;
  • English speaking;
  • Currently reporting heavy drinking;
  • Identifies as a sexual minority woman.

Exclusion criteria

  • Unwilling or unable to provide informed consent;
  • Low literacy (i.e., reporting they "often" or "always" need someone to read instructions, pamphlets, or other written material from a doctor or pharmacy to them)
  • Women who report intention to move away during study period.
  • Active suicidality.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 2 patient groups

Behavioral: Motivational Interview (MI)
Experimental group
Description:
Participants will complete a brief motivational interview focusing on determinants of women's alcohol use, including a focus on normative perceptions as well as motives for drinking.
Treatment:
Behavioral: Behavioral: Motivational Interview (MI)
Behavioral: Health Coaching (HC)
Active Comparator group
Description:
Participants will complete a brief health coaching interview and session focusing on educational modules.
Treatment:
Behavioral: Behavioral: Health Coaching (HC)

Trial contacts and locations

1

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Central trial contact

Alyssa L Norris, PhD

Data sourced from clinicaltrials.gov

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