Variety of Physical Activity in Normal to Overweight Adults Who Are Regularly Active
1 other identifier
observational
50
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started May 2014
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2014
CompletedFirst Submitted
Initial submission to the registry
May 20, 2014
CompletedFirst Posted
Study publicly available on registry
May 29, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedApril 3, 2025
April 1, 2025
4.7 years
May 20, 2014
April 1, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Physical Activity
Baseline, 3 weeks
Study Arms (1)
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.
Eligibility Criteria
Participants will be 50 men and women, recruited from flyers posted on the University of Tennessee-Knoxville campus and in local gyms.
You may qualify if:
- Body mass index (BMI) between 18.5 and 29.9 kg/m2.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Tennessee-Knoxville: Jesse Harris Building
Knoxville, Tennessee, 37996, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Hollie Raynor, PhD
University of Tennessee-Knoxville
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
May 20, 2014
First Posted
May 29, 2014
Study Start
May 1, 2014
Primary Completion
December 31, 2018
Study Completion
December 31, 2025
Last Updated
April 3, 2025
Record last verified: 2025-04