COMPLETED

Decisions During Drinking

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

Decisions during drinking (D3) is randomized clinical feasibility trial assessing whether health-related materials created for young adults who want to have more positive experiences if they decide to drink alcohol are acceptable and usable. Enrolled participants will be randomized to receive the health-related messages in 5-7 online modules over the 20-30 days or to only receive assessments. Those randomized to receive the intervention will also receive text-messages with health message content during the 20-30 days. After completing the intervention, participants will report on the usability and acceptability of the material, which is the main outcome. For secondary outcomes, participants in both the intervention and control will report on their drinking and drinking-related consequences in the post-intervention questionnaire (or 30 days after initial questionnaire for control participants) and 1 month later.

Official Title

Decisions During Drinking: Phase 3 Feasibility Study

Quick Facts

Study Start:2025-04-18
Study Completion:2025-09-10
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06978140

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 24 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Aged 18-24
  2. * At least 1 occurrence of heavy drinking in the past month
  3. * At least 2 alcohol related consequences in the past month
  4. * Live in Washington State
  5. * Agree to be randomized to receive intervention to assessment only control
  6. * Ability to receive SMS text-messages
  7. * Complete Identification verification
  1. * Not meeting inclusion criteria
  2. * Not being able to verify identification

Contacts and Locations

Principal Investigator

Brittney Hultgren, PhD
PRINCIPAL_INVESTIGATOR
University of Washington

Study Locations (Sites)

Center for the Study of Health and Risk Behavior, University of Washington
Seattle, Washington, 98195
United States

Collaborators and Investigators

Sponsor: University of Washington

  • Brittney Hultgren, PhD, PRINCIPAL_INVESTIGATOR, University of Washington

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 Date2025-04-18
Study Completion Date2025-09-10

Study Record Updates

Study Start Date2025-04-18
Study Completion Date2025-09-10

Terms related to this study

Keywords Provided by Researchers

  • alcohol-related consequences

Additional Relevant MeSH Terms

  • Alcohol