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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05180539
Other study ID # Interventional
Secondary ID 5R34AA026032
Status Completed
Phase N/A
First received
Last updated
Start date September 23, 2021
Est. completion date May 8, 2022

Study information

Verified date August 2022
Source Lehigh University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Hazardous alcohol use, sexually transmitted infections, and sexual violence are interrelated and highly prevalent public health concerns in college student populations. The current study seeks to develop a tri-pronged sex-positive intervention that addresses risky alcohol use, unsafe sex, and sexual violence for college men and women (ages 18-24). The study involves a small randomized pilot trial to demonstrate the feasibility and acceptability of the recruitment methods and research design. Preliminary evidence of intervention efficacy will also be evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 217
Est. completion date May 8, 2022
Est. primary completion date May 8, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 24 Years
Eligibility Inclusion Criteria: - Must be student at the site university Exclusion Criteria: - Students who have participated in relevant site specific studies will be excluded

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
SPLASH Intervention Condition
Two-session in person group discussions focusing on behaviors in drinking contexts
Control Condition
Two-session in person group discussions focusing on college health behaviors

Locations

Country Name City State
United States Lehigh University Bethlehem Pennsylvania

Sponsors (3)

Lead Sponsor Collaborator
Lehigh University Brown University, 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 Program Satisfaction as assessed by the Acceptance Questionnaire Satisfaction with the program content. Higher scores indicate more positive evaluations of the program content. Immediate post intervention
Primary Heavy alcohol use Number of standard drinks consumed in a typical week over the past 30 days Change from baseline to 6 month follow-up
Primary Safe Sex Frequency of alcohol use with sex and unprotected sex with casual partners Change from baseline to 6 month follow-up
Primary Bystander Behaviors Willingness Questionnaire Willingness to engage in bystander behaviors. Mean scale scores range from 1 to 7. Higher scores indicate more greater willingness to engage in bystander behaviors. Change from baseline to 6 month follow-up
Primary Bystander Behaviors Self-efficacy Questionnaire Confidence to engage in bystander behaviors. Higher scores indicate more greater confidence in ability to engage in bystander behaviors. Mean scale scores range from 1 to 5. Change from baseline to 6 month follow-up
Secondary Alcohol and sex related protective behavioral strategies use Self-reported frequency of using strategies to reduce alcohol risks and promote positive sexual experiences. Higher scores indicate more frequent use of protective strategies. Change from baseline to 6 month follow-up
Secondary Perceived student drinking norms as assessed by the Drinking Norms Rating Form Perceived descriptive norms are assessed using a variation on the Drinking Norms Rating Form. Respondents estimate the number of standard drinks consumed by other students on their campus for each day in a typical week in the past 30 days; daily estimates are summed to yield perceived number of drinks per week for student peers; range of scores can go from zero to no upper limit Change from baseline to 6 month follow-up
Secondary Perceived student sex norms as assessed by a Sex Norms Questionnaire Respondents estimate the number of high-risk sex behaviors performed by other students on their campus in the past 30 days. Change from baseline to 6 month follow-up
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