ClinicalTrials.Veeva

Menu

Engineering an Online STI Prevention Program

The Pennsylvania State University (PENNSTATE) logo

The Pennsylvania State University (PENNSTATE)

Status

Completed

Conditions

Sexually Transmitted Diseases
Alcohol Consumption
Sexual Behavior

Treatments

Behavioral: Descriptive norms and perceived benefits
Behavioral: Knowledge alone
Behavioral: Expectancies, desc & injun norms, benefits
Behavioral: Descriptive norms alone
Behavioral: Injunctive norms
Behavioral: Expectancies, injunctive norms, benefits, efficacy
Behavioral: Descriptive norms and self-efficacy
Behavioral: Expectancies, descr& injun norms, efficacy
Behavioral: Expectancies and injunctive norms
Behavioral: Descriptive and injunctive norms, benefits
Behavioral: Expectancies and Perceived Benefits
Behavioral: Expectancies and descriptive norms
Behavioral: Expectancies, injunctive norms, and self-efficacy
Behavioral: Injunctive norms and perceived benefits
Behavioral: Expectancies, injunctive norms, benefits
Behavioral: Expectancies, descriptive norms, and self-efficacy
Behavioral: Descriptive norms, injunctive norms,self-efficacy
Behavioral: Self-efficacy alone
Behavioral: Perceived benefits and self-efficacy
Behavioral: Perceived benefits alone
Behavioral: Expectancies, perceived benefits, self-efficacy
Behavioral: Descriptive and injunctive norms
Behavioral: Descriptive norms,perceived benefits,self-efficacy
Behavioral: Injunctive norms and self-efficacy
Behavioral: Expectancies, descriptive and injunctive norms
Behavioral: Expectancies,desc & injun norms,benefits,efficacy
Behavioral: Expectancies, descriptive norms, and benefits
Behavioral: Expectancies alone
Behavioral: Expectancies and self-efficacy
Behavioral: Expectancies,descriptive norms, benefits, efficacy
Behavioral: Injunctive norms, perceived benefits, and self-efficacy
Behavioral: Descriptive and injunctive norms, benefits,efficacy

Study type

Interventional

Funder types

Other

Identifiers

NCT02897804
R01AA022931

Details and patient eligibility

About

The overall objective of the proposed research is to reduce the incidence of sexually transmitted infections (STIs) among college students. The investigators propose to accomplish this by using the innovative, engineering-inspired multiphase optimization strategy (MOST) to develop a highly effective, appealing, economical, and readily scalable internet-delivered behavioral intervention targeting the intersection of alcohol use and sexual risk behavior. The rate of STIs on college campuses is alarming: one in four college students is diagnosed with an STI at least once during their college experience. Sexual activity when drinking alcohol is highly prevalent among college students. Alcohol use is known to contribute to the sexual risk behaviors that are most responsible for the transmission of STIs, namely unprotected sex, contact with numerous partners, and "hook-ups" (casual sexual encounters). Few interventions have been developed that explicitly target the intersection of alcohol use and sexual risk behaviors, and none have been optimized. In order to reduce the incidence of STI transmission among this and other high-risk groups, a new approach is needed. MOST is a comprehensive methodological framework that brings the power of engineering principles to bear on optimization of behavioral interventions. MOST enables researchers to experimentally test the individual components in an intervention to determine their effectiveness, indicating which components need to be revised and re-tested. Given the high rates of alcohol use and sex among college students, the college setting provides an ideal opportunity for intervening on alcohol use and sexual risk behaviors. The proposed study will include a diverse population of college students on 4 campuses which will increase the generalizability of the findings. The specific aims are to (1) develop and pilot test an initial set of online intervention components targeting the link between alcohol use and sexual risk behaviors, (2) use the MOST approach to build an optimized preventive intervention, and (3) evaluate the effectiveness of the newly optimized preventive intervention using a fully powered randomized controlled trial (RCT). This work will result in a new, more potent behavioral intervention that will reduce the incidence of STIs among college students in the US, and will lay the groundwork for a new generation of highly effective STI prevention interventions aimed at other subpopulations at risk.

Full description

As part of the MOST approach, the investigators will conduct a series of screening experiments to build an optimized intervention. The current study is the first (of two) screening experiments.

Enrollment

3,997 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Currently enrolled at an American college or University.
  • A first year student or first-year transfer student.
  • 18 years of age or older.
  • Have not gone through previous versions of itMatters before

Exclusion criteria

  • Not a first year student or transfer student
  • Younger than 18 years of age
  • Have gone through previous versions of itMatters

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

3,997 participants in 32 patient groups

Knowledge alone
Experimental group
Description:
Participants will have access to the knowledge module for a period up to 3 weeks.
Treatment:
Behavioral: Knowledge alone
Self-efficacy alone
Experimental group
Description:
Participants will have access to the knowledge module plus the self-efficacy module for a period up to 3 weeks.
Treatment:
Behavioral: Self-efficacy alone
Perceived benefits alone
Experimental group
Description:
Participants will have access to the knowledge module plus the perceived benefits module for a period up to 3 weeks.
Treatment:
Behavioral: Perceived benefits alone
Benefits and self-efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the perceived benefits and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Perceived benefits and self-efficacy
Injunctive norms alone
Experimental group
Description:
Participants will have access to the knowledge module plus the injunctive norms module for a period up to 3 weeks.
Treatment:
Behavioral: Injunctive norms
Injunctive norms and self-efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the injunctive norms and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Injunctive norms and self-efficacy
Injunctive norms and perceived benefits
Experimental group
Description:
Participants will have access to the knowledge module plus the injunctive norms and perceived benefits modules for a period up to 3 weeks.
Treatment:
Behavioral: Injunctive norms and perceived benefits
Injunctive norms, perceived benefits,self-efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the injunctive norms, perceived benefits, and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Injunctive norms, perceived benefits, and self-efficacy
Descriptive norms alone
Experimental group
Description:
Participants will have access to the knowledge module plus the descriptive norms module for a period up to 3 weeks.
Treatment:
Behavioral: Descriptive norms alone
Descriptive norms and self-efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the descriptive norms and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Descriptive norms and self-efficacy
Descriptive norms and perceived benefits
Experimental group
Description:
Participants will have access to the knowledge module plus the descriptive norms and perceived benefits modules for a period up to 3 weeks.
Treatment:
Behavioral: Descriptive norms and perceived benefits
Descriptive norms,perceived benefits,self-efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the descriptive norms module for a period up to 3 weeks.
Treatment:
Behavioral: Descriptive norms,perceived benefits,self-efficacy
Descriptive norms and injunctive norms
Experimental group
Description:
Participants will have access to the knowledge module plus the descriptive norms and injunctive norms modules for a period up to 3 weeks.
Treatment:
Behavioral: Descriptive and injunctive norms
Descriptive norms, injunctive norms,self-efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the descriptive norms, injunctive norms, and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Descriptive norms, injunctive norms,self-efficacy
Descriptive and injunctive norms, benefits
Experimental group
Description:
Participants will have access to the knowledge module plus the descriptive norms, injunctive norms, and perceived benefits modules for a period up to 3 weeks.
Treatment:
Behavioral: Descriptive and injunctive norms, benefits
Descriptive and injunctive norms, benefits,efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the descriptive norms, injunctive norms, perceived benefits, and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Descriptive and injunctive norms, benefits,efficacy
Expectancies alone
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies module for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies alone
Expectancies and self-efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies and self-efficacy
Expectancies and perceived benefits
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies and perceived benefits modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies and Perceived Benefits
Expectancies, perceived benefits, self-efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, perceived benefits, and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies, perceived benefits, self-efficacy
Expectancies and injunctive norms
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies and injunctive norms modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies and injunctive norms
Expectancies, injunctive norms, and self-efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, injunctive norms, and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies, injunctive norms, and self-efficacy
Expectancies, injunctive norms, and benefits
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, injunctive norms, and perceived benefits modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies, injunctive norms, benefits
Expectancies, injunctive norms, benefits, efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, injunctive norms, perceived benefits, and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies, injunctive norms, benefits, efficacy
Expectancies and descriptive norms
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies and descriptive norms modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies and descriptive norms
Expectancies, descriptive norms, and self-efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, descriptive norms, and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies, descriptive norms, and self-efficacy
Expectancies, descriptive norms, and benefits
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, descriptive norms, and perceived benefits modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies, descriptive norms, and benefits
Expectancies,descriptive norms, benefits, efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, descriptive norms, perceived benefits, and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies,descriptive norms, benefits, efficacy
Expectancies, descriptive and injunctive norms
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, descriptive norms, and injunctive norms modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies, descriptive and injunctive norms
Expectancies, descr& injun norms, efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, descriptive norms, injunctive norms, and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies, descr& injun norms, efficacy
Expectancies, desc & injun norms, benefits
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, descriptive norms, injunctive norms, and perceived benefits modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies, desc & injun norms, benefits
Expectancies,desc & injun norms,benefits,efficacy
Experimental group
Description:
Participants will have access to the knowledge module plus the expectancies, descriptive norms, injunctive norms, perceived benefits, and self-efficacy modules for a period up to 3 weeks.
Treatment:
Behavioral: Expectancies,desc & injun norms,benefits,efficacy

Trial contacts and locations

4

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems