Digitally Prompted Parenting: A Text Message Parent-Based Alcohol Intervention for Incoming College Students

April 15, 2026 updated by: Dr. Joseph LaBrie, Loyola Marymount University
This pilot randomized controlled trial (RCT) will evaluate both the feasibility and efficacy of Digitally Prompted Parenting (DPP), a text-message based parent intervention (tm-PBI) designed to prevent and reduce alcohol use among first-year college students. In this study, parents of incoming first-year students will receive risk-reducing text messages during the first 10 weeks of the Fall semester, which they can forward to their students. The trial uses a longitudinal design to compare drinking outcomes between students whose parents receive the DPP messages and those whose parents receive an established alcohol PBI (the active control condition). The investigators hypothesize that students in the DPP group will report lower levels of alcohol use and fewer alcohol-related consequences after the intervention compared to those in the active control group.

Study Overview

Study Type

Interventional

Enrollment (Actual)

276

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Los Angeles, California, United States, 90045
        • Loyola Marymount

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.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Student is 17-20 years of age
  • Student is an LMU incoming first-year college student
  • Student has access to a cellular device capable of receiving text messages
  • Student's parent or legal guardian has an email address on file at LMU
  • Student's parent or legal guardian has a cellular device capable of receiving text messages
  • Student's parent or legal guardian received an invitation from the research team to participate
  • Student's parent or legal guardian signed up to access the assigned intervention
  • Student's parent or legal guardian is a resident of the United States
  • Informed consent (or assent, as applicable) is provided

Exclusion Criteria:

  • Student is not 17-20 years of age
  • Student is not an LMU incoming first-year college student
  • Student does not have access to a cellular device capable of receiving text messages
  • Student's parent or legal guardian does not have an email address on file at LMU
  • Student's parent or legal guardian does not have a cellular device capable of receiving text messages
  • Student's parent or legal guardian did not receive an invitation from the research team to participate
  • Student's parent or legal guardian did not sign up to access the assigned intervention
  • Student's parent or legal guardian is not a resident of the United States
  • Informed consent (or assent, as applicable) is not provided

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Digitally Prompted Parenting
Parents of participating first-year college students in this intervention arm will receive a series of prewritten text messages during the first 10 weeks of college. Parents can personalize these messages before sending them directly to their student, who is the study participant, with the goal of reducing alcohol-related risks.
Parents will receive an email invitation to sign up for Digitally Prompted Parenting, a text message-delivered PBI. Parents set up an account and input information about themselves and their student, which will customize the text messages they receive. Parents will receive at least two text prompts per week for the first 10 weeks of their student's first semester in college. These texts will (1) prompt parents to call their student to discuss the past week and week ahead, and (2) prompt parents to send an alcohol-specific risk reducing text to their student.
Active Comparator: Active Control
Parents of participating first-year college students in this arm of the study will receive access to the Parent Handbook during the summer before matriculation and three booster emails that summarize its key points after matriculation.
Parents will receive an email that explains the Parent Handbook intervention and includes a link to a website where the Handbook is embedded. They will also receive three booster emails summarizing the key points of the intervention. Parents can review both the Parent Handbook and the booster emails at their own pace.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Daily Drinking between Baseline and 3 Months
Time Frame: baseline, 3 months
Self-reported number of drinks consumed during an average week in the past 30 days.
baseline, 3 months
Change in Daily Drinking between Baseline and 6 Months
Time Frame: baseline, 6 months
Self-reported number of drinks consumed during an average week in the past 30 days.
baseline, 6 months
Change in Peak Drinking Occasion between Baseline and 3 Months
Time Frame: baseline, 3 months
Self-reported max number of drinks consumed on a single occasion in the past 30 days.
baseline, 3 months
Change in Peak Drinking Occasion between Baseline and 6 Months
Time Frame: baseline, 6 months
Self-reported max number of drinks consumed on a single occasion in the past 30 days.
baseline, 6 months
Change in Heavy Episodic Drinking Occasion between Baseline and 3 Months
Time Frame: baseline, 3 months
Self-reported number of times 4/5 drinks (female/male) were consumed in a 2-hour period in the past 30 days.
baseline, 3 months
Change in Heavy Episodic Drinking Occasion between Baseline and 6 Months
Time Frame: baseline, 6 months
Self-reported number of times 4/5 drinks (female/male) were consumed in a 2-hour period in the past 30 days.
baseline, 6 months
Change in Frequency of Intoxication Events between Baseline and 3 Months
Time Frame: baseline, 3 months
Self-reported number of times individuals reported drinking to intoxication in the past 30 days.
baseline, 3 months
Change in Frequency of Intoxication Events between Baseline and 6 Months
Time Frame: baseline, 6 months
Self-reported number of times individuals reported drinking to intoxication in the past 30 days.
baseline, 6 months
Change in Number of Alcohol-Related Consequences between Baseline and 3 Month
Time Frame: baseline, 3 months
Self-reported number of alcohol-related consequences in the past 30 days.
baseline, 3 months
Change in Number of Alcohol-Related Consequences between Baseline and 6 Month
Time Frame: baseline, 6 months
Self-reported number of alcohol-related consequences in the past 30 days.
baseline, 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 Major Dates

Study Start (Actual)

June 27, 2025

Primary Completion (Actual)

March 16, 2026

Study Completion (Actual)

March 16, 2026

Study Registration Dates

First Submitted

March 1, 2025

First Submitted That Met QC Criteria

March 1, 2025

First Posted (Actual)

March 6, 2025

Study Record Updates

Last Update Posted (Actual)

April 16, 2026

Last Update Submitted That Met QC Criteria

April 15, 2026

Last Verified

July 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 1R34AA031358-01A1 (U.S. NIH Grant/Contract)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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