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OverweightNCT02149147

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

An observational study of Overweight, run by The University of Tennessee, Knoxville at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Overweight
How many people
50 participants
Where
1 siteUnited States
Study dates
May 2014to 31 Dec 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

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

Who may be able to join

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

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Tennessee-Knoxville: Jesse Harris Building

    Knoxville, Tennessee, 37996

Other trials in United States

About this study

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.

Read the 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.

Conditions
Overweight
Keywords
physical activity, environmental factors, variety, MVPA
Medical subject headings
Overweight, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT02149147
Study groupRoleWhat they receive
Physical Activity Varietyparticipants 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 being measured

The primary outcome is the main question the study is designed to answer.

  1. Physical Activity

    Measured: Baseline, 3 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 May 2014 (estimated)
  2. Study startMay 2014
  3. Primary completion31 Dec 2018
  4. Study completion31 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02149147
Sponsor's protocol ID
9492 B
Status last verified
Jun 2026
First submitted
20 May 2014
Last updated
9 Jun 2026
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Overweight, run by The University of Tennessee, Knoxville at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 9 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Physical Activity (time frame: Baseline, 3 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jun 2026.

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