Young Adult Education on Alcohol & Health

• Sponsor: University of Washington (Other)
• Overall Status: Not yet recruiting
• CT.gov ID: NCT05620849
• Collaborator: National Institute on Alcohol Abuse and Alcoholism (NIAAA) (NIH)
• Enrollment: 50
• Arm: 1
• Anticipated Duration (Months): 2

Study Details

Study Description

Brief Summary

The goal of this clinical trial is to test whether participants will complete our brief online program (feasibility) and then tell us what it was like going through it (acceptability).

Condition or Disease	Intervention/Treatment	Phase
Sexual Behavior; Alcohol Drinking; Condomless Sex	Behavioral: Online program	N/A

Detailed Description

A total of 50 participants will complete this 5 week study. The study will include a background survey, the 4 week program focused on alcohol and sexual health, and a follow-up survey asking what it was like going through it.

Study Design

• Study Type: Interventional
• Anticipated Enrollment: 50 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Intervention Model Description: All participants will complete the online program.All participants will complete the online program.
• Masking: None (Open Label)
• Primary Purpose: Prevention
• Official Title: A Technology-based Intervention for Alcohol-related Sexual Risk Behaviors in Young Women
• Anticipated Study Start Date: Nov 15, 2022
• Anticipated Primary Completion Date: Jan 15, 2023
• Anticipated Study Completion Date: Jan 15, 2023

Arms and Interventions

Arm	Intervention/Treatment
Other: Intervention group All participants in this pilot trial will receive the intervention	Behavioral: Online program; The online program is 4 weeks and focused on topics such as alcohol and sexual health

Outcome Measures

Primary Outcome Measures

1. Intervention feasibility [Over the course of 5 weeks]

   Feasibility will be assessed as ease of recruitment during the study as well as ability to retain participants during the intervention portion of the study.

2. Acceptability [End of the 5 week study]

   Acceptability will be assessed in the follow-up survey through participant feedback on relevance of the intervention, engagement with the material, skill implementation, suggestions for improvement.

Secondary Outcome Measures

1. Drinking before sex [End of the 5 week study]

   Using items from the Sexual Health Questionnaire, we will assess the quantity and frequency of drinking before sex.

2. Number of sexual partners [End of the 5 week study]

   Using items from the Sexual Health Questionnaire, we will assess number of sexual partners (casual, committed).

3. Condomless sex [End of the 5 week study]

   Using items from the Sexual Health Questionnaire, we will assess the frequency of condom use during penetrative sex.

4. Alcohol use [End of the 5 week study]

   Using the Daily Drinking Questionnaire, we will assess typical drinking quantity and frequency.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 24 Years
• Sexes Eligible for Study: Female
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• Women ages 18-24

• Not engaged or married

• Report an unwanted sexual experience in their lifetime

• Report consuming at least three alcohol drinks per week in past 6 months

• Report heavy episodic drinking (4+ drinks on one occasion) at least once in past 6 months

• Report SRB with men (multiple/casual partners, inconsistent condom use) in the 6 months

• Have a valid email address

Exclusion Criteria:

• Do not want to participate

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

• University of Washington
• National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Investigators

• Principal Investigator: Jessica Blayney, PhD, University of Washington

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Jessica Blayney, Postdoctoral Scholar, School of Medicine: Psychiatry and Behavioral Sciences, University of Washington
• ClinicalTrials.gov Identifier: NCT05620849
• Other Study ID Numbers: STUDY00010940; 1K99AA028777-01
• First Posted: Nov 17, 2022
• Last Update Posted: Nov 17, 2022
• Last Verified: Nov 1, 2022

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Alcohol Drinking

Study Results

No Results Posted as of Nov 17, 2022