RECRUITING

Motivations, Attitudes, and Perceptions Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to compare the impact of providing participants with 1. A recently developed protocol for motivating bystanders to intervene to help others who are in sexual risk situations (Motivate-the-Bystander) alone 2. Motivate-the-Bystander with an alcohol component focused on reducing drinking behaviors (Motivate-the-Bystander+Alcohol) 3. A control condition focused on reducing stress The main questions it aims to answer are: * Is Motivate-the-Bystander more effective than the attention control for increasing bystander behaviors? * Is Motivate-the-Bystander+Alcohol more effective than MTB alone for increasing bystander behaviors? * Is Motivate-the-Bystander+Alcohol more effective than Motivate-the-Bystander alone for decreasing alcohol use during bystander intervention opportunities? Participants will: * Complete online measures (e.g., self-reported bystander behaviors, past bystander training, history of bystander intervention attempts, sexual experiences, drinking behaviors, and other substance use behaviors) * Complete either MTB, MTB+ALC, or the attention control condition online * Complete the virtual reality simulation in the lab * Complete electronic daily diary follow-up surveys about alcohol use and bystander intervention

Official Title

RCT of a Combined MI Intervention to Address Bystander Behaviors in the Context of Alcohol Use

Quick Facts

Study Start:2024-03-01
Study Completion:2026-05-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05873413

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 25 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Individuals ages 18-25
  2. * Heavy drinkers (as defined by using the AUDIT)
  3. * English fluency
  4. * Community members from Lancaster and surrounding counties in Nebraska
  5. * Signed and dated consent form
  6. * Stated willingness to comply with study procedures
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Carrie Murphy
CONTACT
4024723772
carrie.murphy@unl.edu

Principal Investigator

Sarah J Gervais, PhD
PRINCIPAL_INVESTIGATOR
University of Nebraska Lincoln
David DiLillo, PhD
PRINCIPAL_INVESTIGATOR
University of Nebraska Lincoln

Study Locations (Sites)

University of Nebraska-Lincoln
Lincoln, Nebraska, 68588
United States

Collaborators and Investigators

Sponsor: University of Nebraska Lincoln

  • Sarah J Gervais, PhD, PRINCIPAL_INVESTIGATOR, University of Nebraska Lincoln
  • David DiLillo, PhD, PRINCIPAL_INVESTIGATOR, University of Nebraska Lincoln

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-03-01
Study Completion Date2026-05-31

Study Record Updates

Study Start Date2024-03-01
Study Completion Date2026-05-31

Terms related to this study

Additional Relevant MeSH Terms

  • Alcohol Drinking
  • Sexual Violence
  • Social Norms