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Decisions During Drinking (D3)

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University of Washington

Status

Completed

Conditions

Alcohol

Treatments

Behavioral: Personalized feedback

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06978140
STUDY00021311
K01AA027771-05 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Enrollment

35 patients

Sex

All

Ages

18 to 24 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 18-24
  • At least 1 occurrence of heavy drinking in the past month
  • At least 2 alcohol related consequences in the past month
  • Live in Washington State
  • Agree to be randomized to receive intervention to assessment only control
  • Ability to receive SMS text-messages
  • Complete Identification verification

Exclusion criteria

  • Not meeting inclusion criteria
  • Not being able to verify identification

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

35 participants in 2 patient groups

D3 online health information and text-messages
Experimental group
Description:
Participants receiver personalized health information feedback across 5-7 online modules over 20-30 days along with text-message health information
Treatment:
Behavioral: Personalized feedback
Assessment only control
No Intervention group
Description:
Participants will receive questionnaires similar to intervention group but will not receive any health information modules or related text-messages

Trial contacts and locations

1

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Central trial contact

Nicole Fossos-Wong

Data sourced from clinicaltrials.gov

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