Text Message and Competition-Based Interventions Among University Students

February 7, 2024 updated by: Chenyu Zou, Auburn University

Examining the Effects of Text Message and Competition-Based Interventions on Physical Activity, Self-Efficacy, Self-Regulation, Social Support, Incentive Motivation, and Mental Well-being Among University Students

The goal of this quasi-experimental study is to assess and compare the effectiveness of text message interventions and a competition-based intervention and evaluate participants' acceptability and experiences in university students. The main questions it aims to answer are:

  1. What are the effects of text message interventions and competition-based interventions on university students' physical activity levels, self-efficacy, self-regulation, social support, incentive motivation, and mental well-being?
  2. What are participants' perceptions regarding their experience with and acceptability of text message interventions and competition-based interventions?

Participants will

  1. participate in a fitness competition
  2. participate in a fitness competition and receive text messages
  3. enroll in control group

Study Overview

Detailed Description

Physical activity promotes health and wellness, yet many U.S. university students are physically inactive. Text messaging and competition-based interventions have been shown to increase physical activity. The primary objectives of this study are to 1) assess and compare the effectiveness of a competition-based intervention with and without a Social Cognitive Theory-based text-messaging campaign in improving physical activity among university students, and 2) evaluate participants' acceptability and experiences of the text messaging and the competition-based interventions. In coordination with the Deans' Fit Family Challenge (DFFC; an annual physical activity and weight loss competition between Edward Via College of Osteopathic Medicine - Auburn Campus (VCOM-Auburn), Auburn University College of Nursing (AUCON), and Auburn University Harrison College of Pharmacy(HCOP), a 3-group quasi-experimental design will be employed to accomplish the study objectives. A total of 300 students will be enrolled. Students across all 3 institutions who sign up for the DFFC and enroll in this study will be randomly assigned to a competition-only group or a competition + text messaging group. The 3rd group will include students across all 3 institutions who enroll in the study but are not participating in the DFFC.

Participants will submit physical activity minutes via the "Challenge Runner" app, after initially connecting the app to their fitness tracker. All participants will be asked to complete the first anonymous survey at the beginning of the study, as well as the second anonymous survey at the conclusion of the study. Variables of interest include weekly activity minutes, self-efficacy, self-regulation, social support, incentive motivation, mental well-being, participants' acceptability and experiences, and maintenance of moderate and vigorous activity 4 weeks after DFFC. Data will be analyzed using descriptive statistics to characterize the sample and inferential statistics to analyze associations.

Study Type

Interventional

Enrollment (Actual)

58

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

    • Alabama
      • Auburn, Alabama, United States, 36830
        • Auburn University
      • Auburn, Alabama, United States, 36832
        • Edward Via College of Osteopathic Medicine - Auburn Campus

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Auburn University Harrison College of Pharmacy (HCOP), Auburn University College of Nursing (AUCON), and Edward Via College of Osteopathic Medicine - Auburn Campus (VCOM - Auburn) students
  • Possess a smartphone and a fitness tracker or smartwatch
  • Willingness to receive text messages

Exclusion Criteria:

  • Pregnant women
  • Disabilities or chronic diseases that prevent them from being physically active

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: DFFC Group
Students who participated in the 2022 DFFC
An annual 8-week physical activity and weight loss competition between VCOM-Auburn, AU College of Nursing, and AU Harrison School of Pharmacy
Experimental: DFFC + Text Group
Students who participated in the 2022 DFFC and received text messages
An annual 8-week physical activity and weight loss competition between VCOM-Auburn, AU College of Nursing, and AU Harrison School of Pharmacy
Three text messages per week to promote and motive physical activity
No Intervention: Control Group
Students who did not participate in the 2022 DFFC

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Minutes of weekly moderate to vigorous physical activity
Time Frame: week 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Self-reported via the ChallengeRunner online platform
week 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self Efficacy assessed by 9-item Exercise Self Efficacy Scale
Time Frame: week 0 and 8
The Self Efficacy for Exercise scale consists of nine situations (weather, boredom, pain, exercising alone, not pleasurable, too busy, feel tired, stress, depressed) that might effect participation in exercise.
week 0 and 8
Self Regulation assessed by 10-item Self-Regulation Scale
Time Frame: week 0 and 8
A self-report questionnaire to assess attention control in goal pursuit.
week 0 and 8
Social Support assessed by 5-item Friend Support for Exercise Habits Scale
Time Frame: week 0 and 8
Part of the Social Support for Exercise Scale developed by Sallis and colleagues.
week 0 and 8
Incentive Motivation assessed by 23-item Physical Activity Motivation Scale
Time Frame: week 0 and 8
The 23-item Physical Activity Motivation Scale consists of six groups of factors: intrinsic, integrated, identified, introjected, external, and amotivation.
week 0 and 8
Mental Well-Being assessed by The World Health Organization Five Well-Being Index
Time Frame: week 0 and 8
A short self-reported measure of current mental wellbeing.
week 0 and 8
Participants' Experience assessed by questionnaires
Time Frame: week 8
Two multiple choice questions and two open-ended questions
week 8
Participants' Acceptability assessed by questionnaires
Time Frame: week 8
Two 5-point Likert scale questions
week 8

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Race
Time Frame: week 0
week 0
Ethnicity
Time Frame: week 0
week 0
Gender
Time Frame: week 0
week 0
Age
Time Frame: week 0
week 0
Health Literacy assessed by Brief Health Literacy Screening Tool
Time Frame: week 0
The BRIEF consists of the following questions: (1) How often do you have someone help you read hospital materials?"; (2) How confident are you filling out medical forms by yourself?"; (3) "How often do you have problems learning about your medical condition because of difficulty understanding written information?"; and (4) "How often do you have a problem understanding what is told to you about your medical condition?"
week 0

Collaborators and Investigators

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

Investigators

  • Study Director: Brent I Fox, Auburn University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

September 19, 2022

Primary Completion (Actual)

November 11, 2022

Study Completion (Actual)

December 11, 2022

Study Registration Dates

First Submitted

October 21, 2023

First Submitted That Met QC Criteria

January 29, 2024

First Posted (Actual)

February 7, 2024

Study Record Updates

Last Update Posted (Actual)

February 8, 2024

Last Update Submitted That Met QC Criteria

February 7, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 22-380 EX 2209

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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