Exercise Behavior Among Young Adults Study (EBYA)

April 9, 2019 updated by: Phuong Vo, Wayne State University

The rate of adult obesity in the United States has increased more than two times since 1970, and the rate of child-teen obesity has increased by four times. One of the antecedents of obesity is an inactive lifestyle. Exercise has been known to be associated with increases in both physical and mental health by increasing longevity, preventing risk of obesity, coronary heart disease, and hypertension, and increasing self-esteem and overall quality of life. The broad aim of the current study is to investigate the effectiveness of psychoeducational training to increase exercise activity initiation and maintenance in young adults.

The goal of this study is to compare three training approaches for college students to increase exercise behavior. One approach provides general information on the different types of exercises and benefits of engaging in exercise behavior after an initial questionnaire assessment session. A second approach includes the general exercise information and questionnaire assessment as well as training on how to create specific goal intentions (i.e., implementation intentions) to aid in exercise initiation. A third approach uses all the components of the second approach but also tests the utility of a personality-informed module by incorporating concepts from the theory of learned industriousness. It is expected that the third approach will be the most effective in helping participants initiate and maintain their exercise activities during the course of the study duration.

Study Overview

Detailed Description

The aims of the study (mentioned in the Brief Summary) will be addressed using a 6-month multi-wave assessment of approximately 200 college students. Participants will be randomly assigned to one of the three approaches once it is determined they meet study criteria. Random assignment will occur when the participants are scheduled for the first session.

All participants will partake in three group sessions. The first session will take approximately 2 hours to complete. The second and third sessions will be scheduled 2 and 6 months after the first session and will take approximately 45 minutes each to complete.

In the initial session for the first approach, the group session will include discussion of what constitutes regular physical activity and benefits of exercise and basic tips on the activity itself. Guidelines for prescribing suggested exercises will be based on recommendations from the U.S. Department of Health and Human Services as well as risks associated with exercise and how they can be reduced.

In the initial session for the second approach, the group session will include discussion of all the components from the first approach, but with more emphasis on how to create implementation intentions. Discussions will revolve around possible barriers to exercise plans and how to overcome those barriers by making specific plans of when and where to exercise, along with designating which types of exercises they will perform and for how long (or how many repetitions).

In the initial session for the third approach, the group session will include discussion of all the components from the second approach as well as include findings on industriousness. Participants will be directed to think about and generate solutions to how they can become more industrious despite the difficulties they may face and relate these solutions to help them engage in more exercise behavior.

For all approaches, participants will complete questionnaires regarding aspects of their personality, attitudes regarding exercise, beliefs about the positive and negative effects of exercise, confidence in engaging in exercise despite barriers, and current levels of exercise. Participants' body mass index will also be measured. All participants will be given an exercise booklet tailored to their respective approaches to record their exercise behavior during the three weeks following the initial session. They will also be loaned a pedometer that will be used to track their overall daily activities for the same three-week period. Participants in the third approach will also receive booster contacts (to encourage them to think about their efforts and monitoring of physical activity) every two weeks starting after the three-week tracking period until their six-month follow up (total of 11 booster contacts).

The first session will be video and audio recorded to check on and ensure presentation consistency. At the end of the first session, participants will be given a post-session survey to gauge how well materials were presented and to determine how much information participants felt they gained from the session. When participants return their daily exercise diaries and pedometers, they will also complete a condensed set of measures (similar to those in the first session) to track any changes experienced during the three-week tracking period.

For the 2- and 6-month follow-up sessions, participants in all approaches will complete the same questionnaires as in the initial session and have their body mass index measured.

Power analyses conducted via G*Power, 3.1.6 indicated that 159 participants will be needed to detect an effect size of F of 0.25 with alpha error probability at 0.05 and power at 1-Β =.80. Oversampling by 25% will occur to account for possible attrition from the study, thereby making the target N = 200.

Study Type

Interventional

Enrollment (Actual)

221

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

    • Michigan
      • Detroit, Michigan, United States, 48202
        • Wayne State University

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

18 years to 24 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • be currently enrolled in full-time university coursework
  • be between 18 and 24 years old
  • understand and respond to screening questions in English
  • be able to read at a Grade 6 level
  • have adequate health, as assessed by having a body mass index between 18.5 and 29.9 (anyone with a BMI of 30+ is considered obese; National Heart, Lung, & Blood Institute, 2012) to ensure that regular, moderate to intense exercise activity will not negatively affect health
  • identify as individuals who have tried to initiate and continue an exercise regimen sometime in the past but have been unable to maintain the activity
  • indicate the desire to initiate physical activity at the current time
  • be willing to attempt to maintain an exercise schedule during the three-week intervention period to which they will be randomly assigned
  • be willing to participate in the 2-month and 6-month follow up periods

Exclusion Criteria:

  • not already be meeting current USDHHS physical activity recommendations (i.e., at least 150 minutes of moderate-intensity exercise per week)
  • not have major cognitive impairments (i.e., assessed by whether they can understand and respond adequately to all screening questions)
  • not report consuming more than three (women) or four (men) alcoholic drinks per day (as this may interfere with their ability to engage in physical activity and confound study results)
  • not be pregnant
  • not have children
  • not have preexisting physical limitations or recent injuries
  • not have major cognitive impairments (i.e., assessed by whether they can understand and respond adequately to all screening questions)

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Sham Comparator: Exercise info only
Participants in the "exercise information only" group will engage in a group discussion with the principal investigator to discuss what constitutes regular physical activity and benefits of exercise and basic tips on the activity itself. Guidelines for prescribing suggested exercises will be based on recommendations from the U.S. Department of Health and Human Services (USDHHS, 2008) as well as risks associated with exercise and how they can be reduced.

Discussion:

  • benefits of exercise
  • types of exercise
  • exercise guidelines
  • components of an exercise session
  • how to reduce risk of injuries
Experimental: Exercise info + implementation intentions
Participants in the "exercise information plus implementation intentions" group will engage in a group discussion with the principal investigator to discuss all of the components from the exercise information only approach, but with more emphasis on how to create implementation intentions. Discussions will revolve around possible barriers to exercise plans and how to overcome/address those barriers by making specific plans of when and where to exercise, along with designating which types of exercises they will perform and for how long (or how many repetitions).

Discussion:

  • benefits of exercise
  • types of exercise
  • exercise guidelines
  • components of an exercise session
  • how to reduce risk of injuries

Discussion of:

  • barriers to exercise and how to address/overcome barriers
  • how to create detailed exercise plans
Experimental: Exercise info + implementation intentions + industriousness
Participants in the "exercise information plus implementation intentions plus industriousness training" group will engage in a group discussion with the principal investigator to discuss all of the components from the second approach as well as include findings linking industriousness and exercise behavior. Participants will be directed to think about and generate solutions to how they can become more industrious and monitor their efforts despite the difficulties they may face and relate these solutions to help them engage in more exercise behavior.

Discussion:

  • benefits of exercise
  • types of exercise
  • exercise guidelines
  • components of an exercise session
  • how to reduce risk of injuries

Discussion of:

  • barriers to exercise and how to address/overcome barriers
  • how to create detailed exercise plans

Discussion of:

  • realistic monitoring of efforts related to exercise
  • reaching and pushing past thresholds for sustained effort for exercise

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total Physical Activity
Time Frame: 2-3 months after initial intervention session

The Godin Leisure-Time Exercise Questionnaire (GLTEQ; Godin & Shephard, 1985) was used to assess the frequency of typical weekly strenuous, moderate, and mild exercise (open-ended format). Total exercise scores were also computed by multiplying each reported exercise frequency by its metabolic equivalent (MET) and then summing the totals: (strenuous x 9) + (moderate x 5) + (mild x 2) (Godin, Jobin, & Boullon, 1986). Higher scores on this scale indicates more exercise engagement.

Also, participants were loaned a pedometer to obtain objective measures of exercise activity. The pedometers allow participants to enter their weight and height and measure steps taken throughout the day based on this information. The devices automatically reset at midnight and store the information for 30 days.

2-3 months after initial intervention session
Total Physical Activity
Time Frame: 6 months after initial intervention session

The Godin Leisure-Time Exercise Questionnaire (GLTEQ; Godin & Shephard, 1985) was used to assess the frequency of typical weekly strenuous, moderate, and mild exercise (open-ended format). Total exercise scores were also computed by multiplying each reported exercise frequency by its metabolic equivalent (MET) and then summing the totals: (strenuous x 9) + (moderate x 5) + (mild x 2) (Godin, Jobin, & Boullon, 1986). Higher scores indicate more exercise engagement.

Also, participants were loaned a pedometer to obtain objective measures of exercise activity. The pedometers allow participants to enter their weight and height and measure steps taken throughout the day based on this information. The devices automatically reset at midnight and store the information for 30 days.

6 months after initial intervention session

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Exercise Self-efficacy
Time Frame: 2-3 months after initial intervention session
The 18-item multidimensional exercise self-efficacy scale (Benisovich, Rossi, Norman, & Nigg, 1998) assessed participants' confidence in being able to exercise despite bad weather, inconvenience, negative affect, exercising alone, excuse making, and resistance from others. Participants were asked to rate "how confident [they] are to exercise when other things get in the way" on a 5-point Likert scale (1 = Not at all confident, 5 = Extremely confident). Example items include, "I don't have access to exercise equipment," "I don't feel like it," and "I am spending time with friends or family who do not exercise." All items on the scale were averaged for each participant. Higher scores indicate greater self-efficacy for exercise.
2-3 months after initial intervention session
Exercise Self-efficacy
Time Frame: 6 months after initial intervention session
The 18-item multidimensional exercise self-efficacy scale (Benisovich, Rossi, Norman, & Nigg, 1998) assessed participants' confidence in being able to exercise despite bad weather, inconvenience, negative affect, exercising alone, excuse making, and resistance from others. Participants were asked to rate "how confident [they] are to exercise when other things get in the way" on a 5-point Likert scale (1 = Not at all confident, 5 = Extremely confident; αs = .89-.91 across assessments). Example items include, "I don't have access to exercise equipment," "I don't feel like it," and "I am spending time with friends or family who do not exercise." All items on the scale were averaged for each participant. Higher scores indicate greater self-efficacy.
6 months after initial intervention session

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Industriousness Level
Time Frame: 2-3 months after initial intervention session
Industriousness was assessed using a 10-item Industriousness scale (Chernyshenko, 2003). Participants rated themselves on a 5-point Likert scale (1 = Disagree strongly, 5 = Agree strongly) indicating the extent to which, for example, they are someone who "has high standards and works toward them; setting goals and achieving them is not very important to me [reversed], [or] invests little effort into my work [reversed] ". Higher scores indicate greater industriousness level.
2-3 months after initial intervention session
Industriousness Level
Time Frame: 6 months after initial intervention session
Industriousness was assessed using a 10-item Industriousness scale (Chernyshenko, 2003). Participants rated themselves on a 5-point Likert scale (1 = Disagree strongly, 5 = Agree strongly) indicating the extent to which, for example, they are someone who "has high standards and works toward them; setting goals and achieving them is not very important to me [reversed], [or] invests little effort into my work [reversed] ". Higher scores indicate greater industriousness level.
6 months after initial intervention session

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Phuong T Vo, BA, Wayne State University
  • Study Director: Tim D Bogg, PhD, Wayne State 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.

General Publications

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

August 1, 2013

Primary Completion (Actual)

May 1, 2016

Study Completion (Actual)

May 1, 2016

Study Registration Dates

First Submitted

July 25, 2014

First Submitted That Met QC Criteria

July 29, 2014

First Posted (Estimate)

July 30, 2014

Study Record Updates

Last Update Posted (Actual)

May 3, 2019

Last Update Submitted That Met QC Criteria

April 9, 2019

Last Verified

April 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 072613B3F

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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