ClinicalTrials.gg
CompletedNCT06861660Updated Apr 16, 2026

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

An interventional study of Digitally Prompted Parenting and Active Control in Underage Drinking, sponsored by Loyola Marymount University. Completed at 1 site in United States. Open to participants aged 17 Years to 20 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-16.

Sponsored by Loyola Marymount University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
276
Allocation
Randomized
Ages
17 Years to 20 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Underage Drinking

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03

In context

Underage Drinking

44 studies on the registry are indexed under Underage Drinking; 13 are open to participants now.

This study's enrollment of 276 is below the median of 360 across 43 interventional studies indexed under Underage Drinking.

Browse Underage Drinking studies →

Lead sponsor

Loyola Marymount University is the lead sponsor of 9 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
17 Years to 20 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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
  • (or assent, as applicable) is provided

Exclusion criteria

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
  • (or assent, as applicable) is not provided
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
276 participants (actual)

Study arms

  • 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.

    Behavioral: Digitally Prompted Parenting

  • 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.

    Behavioral: Active Control

Interventions

  • BehavioralDigitally Prompted Parenting

    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.

  • BehavioralActive Control

    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.

06

What researchers measure

Primary outcomes

  1. Change in Daily Drinking between Baseline and 3 Months

    Self-reported number of drinks consumed during an average week in the past 30 days.

    Time frame: baseline, 3 months

  2. Change in Daily Drinking between Baseline and 6 Months

    Self-reported number of drinks consumed during an average week in the past 30 days.

    Time frame: baseline, 6 months

  3. Change in Peak Drinking Occasion between Baseline and 3 Months

    Self-reported max number of drinks consumed on a single occasion in the past 30 days.

    Time frame: baseline, 3 months

  4. Change in Peak Drinking Occasion between Baseline and 6 Months

    Self-reported max number of drinks consumed on a single occasion in the past 30 days.

    Time frame: baseline, 6 months

  5. Change in Heavy Episodic Drinking Occasion between Baseline and 3 Months

    Self-reported number of times 4/5 drinks (female/male) were consumed in a 2-hour period in the past 30 days.

    Time frame: baseline, 3 months

  6. Change in Heavy Episodic Drinking Occasion between Baseline and 6 Months

    Self-reported number of times 4/5 drinks (female/male) were consumed in a 2-hour period in the past 30 days.

    Time frame: baseline, 6 months

  7. Change in Frequency of Intoxication Events between Baseline and 3 Months

    Self-reported number of times individuals reported drinking to intoxication in the past 30 days.

    Time frame: baseline, 3 months

  8. Change in Frequency of Intoxication Events between Baseline and 6 Months

    Self-reported number of times individuals reported drinking to intoxication in the past 30 days.

    Time frame: baseline, 6 months

  9. Change in Number of Alcohol-Related Consequences between Baseline and 3 Month

    Self-reported number of alcohol-related consequences in the past 30 days.

    Time frame: baseline, 3 months

  10. Change in Number of Alcohol-Related Consequences between Baseline and 6 Month

    Self-reported number of alcohol-related consequences in the past 30 days.

    Time frame: baseline, 6 months

07

Study locations

1 site
  • Loyola Marymount
    Los Angeles, California 90045, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06861660
Lead sponsor
Loyola Marymount University
Responsible party
Dr. Joseph LaBrie (Principal Investigator, Loyola Marymount University) — Principal investigator
First posted
Mar 6, 2025
Start date
Jun 27, 2025
Primary completion
Mar 16, 2026
Completion
Mar 16, 2026
Last update
Apr 16, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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