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Motivating Campus Change Study

NCT ID: NCT04030325

Last Updated: 2024-12-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

1012 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-11-06

Study Completion Date

2025-06-30

Brief Summary

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The study evaluates the relative merit of a multi-component PFI presented in the traditional simultaneous delivery (i.e., all components at once) versus a sequential format, wherein individual PFI components are delivered one at a time over several weeks to minimize time and attention demands for each component.

Detailed Description

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This study builds upon the latest alcohol intervention literature to develop and test the next wave of personalized feedback interventions (PFIs) to address harmful alcohol use among college students. The purpose of this research is to determine optimal configuration of PFIs to take advantage of the clarity and initial impact of single-component PFIs and greater effect size and duration of personalized multi-component PFIs. The Investigators seek to increase and evaluate engagement with the PFI and text-message materials and boost innovation of both content and process of the intervention. In addition to PFI content and delivery, the investigators will use qualitative and quantitative methods to determine personal relevance of the chosen high-risk events among a sample of students who engage in heavy episodic drinking to better understand duration of PFI effects impacted by fluctuations in drinking associated with high-risk events. Prior interventions have targeted drinking in general or a single high-risk drinking event (e.g., Spring Break), but have not targeted both general and event-specific drinking together. These enhanced intervention effects, could have a significant impact on risks associated with college student drinking, and can be rapidly disseminated and implemented on campuses nationwide to address the public health problem posed by heavy episodic drinking among college students.

Conditions

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Drinking Behavior

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Sequential Post Feedback Information Delivery

Participants receive the first component of their PFI immediately following Baseline and subsequently receive 1 component each week until they receive all 4 components. Participants will complete a Post Feedback Survey and a 3 week follow back and Knowledge assessment.

Group Type EXPERIMENTAL

Sequential Personalized Feedback Intervention Delivery

Intervention Type BEHAVIORAL

Sequential PFI delivery over 3 weeks after baseline survey

Sequential Post Feedback Information Delivery +Text Messages

Participants receive the first component of their PFI immediately following Baseline and subsequently receive 1 component each week until they receive all 4 components. Participants will complete a Post Feedback Survey and a 3 week follow back and Knowledge assessment. Additionally, participants receive the Text Message Booster Component in the days before and during the high risk drinking event celebration(s).

Group Type EXPERIMENTAL

Sequential Personalized Feedback Intervention Delivery

Intervention Type BEHAVIORAL

Sequential PFI delivery over 3 weeks after baseline survey

Text Message Boosters

Intervention Type BEHAVIORAL

Text message boosters on PFI content during week of high risk drinking events

Simultaneous Post Feedback Information Delivery

Participants receive all 4 feedback components immediately after providing consent to the Pilot Feasibility Study following the Screening/Baseline Survey. Participants complete a brief 10 minute Post-Feedback Survey and a 3 Week Followup Survey to assess knowledge of the intervention feedback content.

Group Type EXPERIMENTAL

Simultaneous Personalized Feedback Intervention Delivery

Intervention Type BEHAVIORAL

Simultaneous PFI delivery after baseline survey

Simultaneous Post Feedback Information Delivery +Text Messages

Participants receive all 4 feedback components immediately after providing consent to the Pilot Feasibility Study following the Screening/Baseline Survey. Participants complete a brief 10 minute Post-Feedback Survey and a 3 Week Followup Survey to assess knowledge of the intervention feedback content. Additionally, participants receive the Text Message Booster Component in the days before and during the high risk drinking event celebration(s).

Group Type EXPERIMENTAL

Simultaneous Personalized Feedback Intervention Delivery

Intervention Type BEHAVIORAL

Simultaneous PFI delivery after baseline survey

Text Message Boosters

Intervention Type BEHAVIORAL

Text message boosters on PFI content during week of high risk drinking events

Assessment Only Control

Participants complete baseline survey, longitudinal follow up assessments, and pre- and post- event surveys.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Sequential Personalized Feedback Intervention Delivery

Sequential PFI delivery over 3 weeks after baseline survey

Intervention Type BEHAVIORAL

Simultaneous Personalized Feedback Intervention Delivery

Simultaneous PFI delivery after baseline survey

Intervention Type BEHAVIORAL

Text Message Boosters

Text message boosters on PFI content during week of high risk drinking events

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* at least 1 heavy episodic drinking episode in the past month
* at least 3 negative alcohol related consequences on Rutgers Alcohol Problem Index/ Young Adult Alcohol Problems Screening Test in the past 3 months for cohort 1
* at least 2 negative alcohol related consequences on Rutgers Alcohol Problem Index/ Young Adult Alcohol Problems Screening Test in the past month for cohort 2 - 5
* Indicate they own a cell phone with text message capabilities and consent to receiving text messages

* Unwillingness to participate
* Failure to provide consent
* Plan to travel internationally in the next 12 months (for intervention text purposes)
Minimum Eligible Age

18 Years

Maximum Eligible Age

24 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute on Alcohol Abuse and Alcoholism (NIAAA)

NIH

Sponsor Role collaborator

University of Washington

OTHER

Sponsor Role lead

Responsible Party

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Mary Larimer

Professor, School of Medicine: Psychiatry And Behavioral Sciences

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mary E Larimer, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Washington

Locations

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The Center for the Study of Health and Risk Behaviors

Seattle, Washington, United States

Site Status

Countries

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United States

Other Identifiers

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R37AA012547-11A1

Identifier Type: NIH

Identifier Source: secondary_id

View Link

STUDY00007499

Identifier Type: -

Identifier Source: org_study_id