Variety of Physical Activity in Normal to Overweight Adults Who Are Regularly Active

June 17, 2023 updated by: Hollie Raynor, The University of Tennessee, Knoxville
The purpose of this study is to investigate the variety of physical activity, a cross-sectional design will be used. The data collected will provide descriptive details about how people are engaging in physical activity, as well details about the environment they are in while engaging in physical activity.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

Many individuals, particularly those who are obese, are inactive and increasing physical activity continues to be a challenge, thus, developing strategies that assist individuals in engaging and sustaining high levels of physical activity is imperative.1,2 Incorporating a variety of activities into a physical activity program is a strategy that may be promising for increasing physical activity levels.3 Data from the National Health and Nutrition Examination Survey (NHANES) showed that individuals who reported engaging in a variety of activities (i.e., walking + other leisure-time activities) were more likely to meet national physical activity recommendations compared to those who reported no variety (i.e., only walking).4 In another study, the investigators found that overweight participants in an 18-month behavioral lifestyle intervention who reported physical activity variety (i.e., ≥ 2 activities) at 6 months had higher self-reported physical activity-related energy expenditure and a lower body mass index (BMI) at 18 months than those who reported no physical activity variety (i.e., only 1 activity).5 Additionally, the investigators have also found that performing a variety of activities is related to greater engagement in objectively measured moderate- to vigorous-intensity physical activity in both successful weight loss maintainers and normal weight individuals.6 Based on the literature available, it appears that increasing the number of activities in a physical activity regimen can assist with increasing engagement of physical activity. However, physical activity variety has primarily been examined by summing the number of different activities a person engages in (i.e., walking + other leisure-time activities). Other environmental factors, including location, visual and auditory stimuli, and the number and types of people engaging in physical activity in close proximity, may impact on the degree of variety of differing physical activities that people engage in. Thus, the purpose of this study is to collect more information about physical activity variety.

Specific Aims:

Specific Aim 1. To determine the average minutes of moderate- to vigorous-intensity physical activity participants engage in.

Specific Aim 2. To determine if environmental factors influence the degree of variety of physical activities that participants engage in.

Specific Aim 3. To determine if the average number of minutes of moderate- to vigorous-intensity physical activity increases as the variety of physical activities increases.

Study Type

Observational

Enrollment (Estimated)

50

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

    • Tennessee
      • Knoxville, Tennessee, United States, 37996
        • University of Tennessee-Knoxville: Jesse Harris Building

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 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Participants will be 50 men and women, recruited from flyers posted on the University of Tennessee-Knoxville campus and in local gyms.

Description

Inclusion Criteria:

  • Body mass index (BMI) between 18.5 and 29.9 kg/m2.

Exclusion Criteria:

  • Have a metal allergy (which would prevent the ability of a participant to wear the SenseWear® armband from BodyMedia® used in the proposed study).
  • Self-report engaging in less than 30 minutes/week of moderate- to vigorous-intensity physical activity over the previous week.

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

Cohorts and Interventions

Group / Cohort
Physical Activity Variety
participants will complete the Self-Efficacy questionnaire, the Physical Activity Enjoyment Scale, the Behavioral Regulation in Exercise-2 questionnaire, and an Outcome Expectations questionnaire. Participants will be instructed to wear the SenseWear® armband which will measure physical activity-related energy expenditure for the course of the study. The armband will be worn every day for at least 10 hours per day. In addition, participants will be asked to complete a physical activity diary to record their physical activity as well as additional information about the environment in which the physical activity was conducted. Participants will be instructed to engage in their normal physical activity regimen, wear the armband, and complete the physical activity diary for 3 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Physical Activity
Time Frame: Baseline, 3 weeks
Baseline, 3 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Hollie Raynor, PhD, University of Tennessee-Knoxville

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

May 1, 2014

Primary Completion (Actual)

December 31, 2018

Study Completion (Estimated)

December 31, 2024

Study Registration Dates

First Submitted

May 20, 2014

First Submitted That Met QC Criteria

May 28, 2014

First Posted (Estimated)

May 29, 2014

Study Record Updates

Last Update Posted (Actual)

June 22, 2023

Last Update Submitted That Met QC Criteria

June 17, 2023

Last Verified

June 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 9492 B

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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