Skip to main content
Clinical Trials/NCT06861660
NCT06861660CompletedNot Applicable

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

Loyola Marymount University1 site in 1 country276 target enrollmentStarted: June 27, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
276
Locations
1
Primary Endpoint
Change in Daily Drinking between Baseline and 3 Months

Study Overview

Brief 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Participant)

Masking Description

Study conditions are randomly assigned and the intervention delivery is automated. Senior members of the research team will have a record of the participants randomized to each condition, but the delivery of intervention content is automated. Junior members of the research team responsible for sending follow-up survey reminders will not be aware of participant condition assignment.

Eligibility Criteria

Ages
17 Years to 20 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Arms & Interventions

Digitally Prompted Parenting

Experimental

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.

Intervention: Digitally Prompted Parenting (Behavioral)

Active Control

Active Comparator

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.

Intervention: Active Control (Behavioral)

Outcomes

Primary Outcomes

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr. Joseph LaBrie

Principal Investigator

Loyola Marymount University

Study Sites (1)

Loading locations...

Similar Trials