Physical Activity Variety's Impact on Physical Activity Participation

January 6, 2025 updated by: University of Minnesota
The primary purpose of the proposed study is to examine the effect of a home-based physical activity variety intervention on objectively measured physical activity in an eight-week randomized intervention trial.

Study Overview

Detailed Description

The primary purpose of the proposed study is to examine the effect of a home-based physical activity variety intervention on objectively measured physical activity in an eight-week randomized intervention trial. Early research on physical activity variety has observed increased physical activity participation, motivation, and enjoyment as a result of physical activity variety. However, previous studies examining variety have not included home-based interventions, objective measures of physical activity, or cardiovascular fitness classes.

Forty low-active college students will be randomly assigned to either an eight-week physical activity variety intervention (n=20) or a physical activity consistency comparison condition (n=20). Physical activity will be assessed via an accelerometer (e.g., Actigraph) at baseline and eight weeks, and psychosocial variables at baseline, four weeks, and eight weeks (i.e., post-intervention). Affect will be assessed at one, four, and eight weeks. Participants will receive counseling sessions and access to a website containing workouts appropriate to their condition.

Study Type

Interventional

Enrollment (Actual)

47

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

    • Minnesota
      • Minneapolis, Minnesota, United States, 55414
        • University of Minnesota

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Engaged in no or low levels of physical activity (less than 90 minutes of moderate to vigorous intensity physical activity per week)
  • Capable of completing a 30-minute session of physical activity
  • 18-25 years of age old

Exclusion Criteria:

  • Pregnant individuals
  • Cannot read in English
  • No access to the internet
  • Healthcare providers have instructed them not to be active
  • Any medical condition that would make physical activity unsafe or unwise

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Physical activity variety intervention
Participants in the variety condition will be sent the link to their condition's website via email. The variety website will contain nine distinct high intensity interval training (HIIT) videos. The videos will be 30-minutes containing a five-minute warm-up, 20-minute workout, and a five-minute cool down. The website will emphasize the importance of having variety in one's physical activity routine. This will include reminders to have variety in selected workouts and the benefits associated with doing so. This emphasis will be supported through the counseling sessions provided to participants in the variety condition.
The counseling in the variety condition will serve many purposes. The first session will concentrate on informing participants on the importance of having variety in their physical activity routine and how to access the variety of physical activities available to them. The variety condition will be instructed to complete at least three different HIIT workouts per week. They will be encouraged to complete more than three workouts. The following counseling sessions will be provided to not only continue supporting variety in physical activity but also to support participants' basic psychological needs.
Active Comparator: Physical activity consistency comparison condition
Upon the completion of randomization, participants in the consistency condition will be sent the link to their condition's website via email. The consistency website will contain one HIIT video. The video will be 30-minutes and include a five-minute warm-up, 20-minute workout, and a five-minute cool down. The website will emphasize the importance of having consistency in one's physical activity routine. This will include reminders to be consistent in workouts and the benefits associated with doing so (Guiney & Machado, 2013). This emphasis will be supported through the counseling sessions provided to participants in the consistency condition.
The counseling in the consistency condition will serve many purposes. The first session will concentrate on informing participants the importance of having consistency in their physical activity routine and how to access the HIIT workout available to them. The consistency condition will be instructed to complete the provided HIIT workout three times per week. They will be encouraged to complete more than three workouts. The following counseling sessions will be provided to not only continue supporting consistency in physical activity but also to support participants' basic psychological needs.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Actigraph
Time Frame: Measuring the change from baseline to week 8.
An electronic device worn on the right hip to identify motion.
Measuring the change from baseline to week 8.
Actigraph
Time Frame: Measuring the change from baseline to week 8.
An electronic device worn on the right hip to identify steps taken.
Measuring the change from baseline to week 8.
Actigraph
Time Frame: Measuring the change from baseline to week 8.
An electronic device worn on the right hip to identify energy expenditure.
Measuring the change from baseline to week 8.
Actigraph
Time Frame: Measuring the change from baseline to week 8.
An electronic device worn on the right hip to identify time spent in different intensities of activity.
Measuring the change from baseline to week 8.
7-Day Physical Activity Recall Interview
Time Frame: Measuring change weekly from baseline until the eighth week of the intervention.
Allows for tracking all bouts of MVPA that are at least 10 minutes in duration over the previous week. Physical activity is reported as minutes spent in moderate, hard, and very hard activities.
Measuring change weekly from baseline until the eighth week of the intervention.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Behavioral Regulation in Exercise Questionnaire (BREQ-2)
Time Frame: At baseline, weeks 4, and 8.
Questionnaire: The BREQ-2 will assess participants' motivation regarding physical activity including amotivation, external regulation, introjected regulation, identified regulation, intrinsic regulation, and intrinsic motivation towards physical activity. The BREQ-2 is 19 items that includes a five-point Likert scale ranging from 0-4 with zero indicating "is not true" and four "very true." The BREQ-2 is a validated and commonly used measure examining SDT constructs.
At baseline, weeks 4, and 8.
Motives for Physical Activity Measure-Revised (MPAM-R)
Time Frame: At baseline, weeks 4, and 8.
Questionnaire: The MPAM-R will be administered to assess participants' motives for physical activity. The five areas of motivation that are assessed include the following: Interest/enjoyment, competence, appearance, fitness, and social. Participants indicate how true an item is regarding why they engage in physical activity. Examples of the 30 items include, "It is fun," "I want to maintain physical strength for a healthy life," and "I like to be with others interested in this activity." The MPAM-R includes a Likert scale ranging from 1-7, with one indicating "not at all true" and a seven "very true." This measure has been validated for measuring motives for physical activity.
At baseline, weeks 4, and 8.
Psychological Need Satisfaction in Exercise (PNSE)
Time Frame: At baseline, weeks 4, and 8.
Questionnaire: The PNSE will assess participants' satisfaction of their psychological needs, competence, autonomy, and relatedness. This measure is 18-items with six items examining each psychological need. An example of one item included for perceived competence is, "I feel that I am able to complete exercises that are personally challenging." An example of one item for perceived autonomy is, "I feel free to exercise in my own way." Lastly, one example of an item included for perceived relatedness is, "I feel attached to my exercise companions because they accept me for who I am." The items are scored using a Likert scale ranging from 1-6 with a one indicating "false" and a six representing "true." Higher values signify greater satisfaction of psychological needs. The PNSE has high reliability and is a commonly used measure for basic psychological needs.
At baseline, weeks 4, and 8.
Physical Activity Enjoyment Scale (PACES)
Time Frame: At baseline, weeks 4, and 8.
Questionnaire: The PACES will assess participants' physical activity enjoyment. The PACES is an 18-item measure instructing participants to, "Measure how they feel about physical activity at this moment in time...." Participants rate each item using a Likert scale ranging from 1-7 with one and seven reflecting opposite ends of the spectrum. For example, the two anchors for the first item are, "I enjoy it" and "I hate it." In this example, a one aligns with "I enjoy it" and a seven aligns with "I hate it." Eleven of the items are reverse scored. Higher scores indicate higher levels of physical activity enjoyment. This measure has been found to be reliable and valid.
At baseline, weeks 4, and 8.
Bored of Sports Scale (BOSS)
Time Frame: At baseline, weeks 4, and 8.
Questionnaire: The BOSS is a newly developed scale to assess boredom in physical activity. The BOSS is 11 items and includes a five-point Likert scale ranging from 0-4, with one representing "strongly disagree" and four representing "strongly agree." An example of an item is, "Exercising is dull and monotonous." Participants respond to prompts regarding their boredom in a specific bout of physical activity. This measure has been found to be reliable.
At baseline, weeks 4, and 8.
Exercise-Induced Feeling Inventory (EFI)
Time Frame: At baseline, weeks 4, and 8.
Questionnaire: The EFI will assess exercise feeling. The 12-item questionnaire instructs participants to, "Indicate how each word describes how they feel at this moment in time...." Participants rate how they feel on a Likert scale of 0-4 with a zero indicating an item is "not felt;" whereas, a four indicates an item is "felt very strongly." Examples of the items are "refreshed," "worn out," and "energetic." The EFI is scored by summing the four subscales, which include revitalization, physical exhaustion, positive engagement, and tranquility. The four subscales each consist of three items. The EFI has demonstrated good internal consistency and reliability.
At baseline, weeks 4, and 8.
Feeling Scale (FS)
Time Frame: At weeks 1, 4, and 8.
Questionnaire: The FS will assess affective valence experienced during physical activity. The FS is a two-item questionnaire that measures how participants are feeling and how much they are enjoying or enjoyed exercise. Participants rate their current feeling before, during, and after physical activity as part of the FS-current using a scale of -5 to +5, with a higher score indicating higher levels of positive affect. They rate their enjoyment as part of the FS-enjoyment on a scale of 1-7, with higher scores reflecting higher enjoyment. The FS is reliable for assessing in-exercise affect.
At weeks 1, 4, and 8.

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceived Exercise Variety (PVE)
Time Frame: At baseline, weeks 4, and 8.
Questionnaire: The PVE questionnaire will assess perceived variety of physical activity. Participants are asked to, "Please answer the following questions by considering how you typically feel while you are exercising." The questionnaire includes five items such as, "I feel like my exercise program is varied" and includes a 1-6 Likert scale with one indicating an item to be false and six indicating an item to be true. The PVE has been found to be valid and reliable.
At baseline, weeks 4, and 8.

Collaborators and Investigators

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

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 1, 2023

Primary Completion (Actual)

June 3, 2024

Study Completion (Actual)

June 3, 2024

Study Registration Dates

First Submitted

May 12, 2023

First Submitted That Met QC Criteria

June 25, 2023

First Posted (Actual)

July 5, 2023

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 6, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The Principal Investigator will be the only person with the authority to release the collected data. Confidential information will not be released under any circumstance. The original data file will stay in its original slate.

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.

Clinical Trials on Physical Inactivity

Clinical Trials on Physical activity variety intervention

Subscribe