RECRUITING

mHealth Behavior 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 learn if a brief task completed on a smartphone can reduce alcohol use and risky sexual behavior among women between the ages of 18 and 25 who have a history of experiencing sexual assault or an unwanted sexual experience. The main questions it aims to answer are: * Does the smartphone task change approach biases for alcohol and condom-related images? * Does the smartphone task reduce alcohol use and risky sexual behavior? Researchers will compare the smartphone task to a sham control to see if the smartphone task changes biases and behavior. Participants will: * Complete a baseline assessment battery of questionnaires * Complete either the intervention smartphone task or the sham smartphone task on four consecutive days. * Complete a follow-up assessment one week after finishing the four tasks * Complete a three-month follow-up

Official Title

Mobile Health Reaction Time and Behavior Study

Quick Facts

Study Start:2025-01-29
Study Completion:2025-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06624514

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:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adult women who report lifetime experience sexual assault,
  2. * Consume alcohol at least moderately (e.g., at least seven drinks per week; NIAAA, 2015),
  3. * Have engaged in sexual intercourse with a casual, non-committed male partner without a condom at least three times during the three months prior to data collection.
  1. * Active homicidal or suicidal ideation;
  2. * History of or current psychotic disorders as the study protocol may be therapeutically insufficient;
  3. * Previously identified as having a Pervasive Developmental Disability.

Contacts and Locations

Study Contact

Amy Boatright
CONTACT
843-779-2552
boatrigh@musc.edu

Principal Investigator

Austin Hahn, PhD
PRINCIPAL_INVESTIGATOR
Medical University of South Carolina

Study Locations (Sites)

Medical University of South Carolina
Charleston, South Carolina, 29425
United States

Collaborators and Investigators

Sponsor: Medical University of South Carolina

  • Austin Hahn, PhD, PRINCIPAL_INVESTIGATOR, Medical University of South Carolina

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 Date2025-01-29
Study Completion Date2025-11

Study Record Updates

Study Start Date2025-01-29
Study Completion Date2025-11

Terms related to this study

Keywords Provided by Researchers

  • Alcohol
  • condoms
  • Sexual Assault
  • Risky Sex

Additional Relevant MeSH Terms

  • Alcohol Consumption
  • Condom Use