- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02149147
Variety of Physical Activity in Normal to Overweight Adults Who Are Regularly Active
Study Overview
Status
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
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
Tennessee
-
Knoxville, Tennessee, United States, 37996
- University of Tennessee-Knoxville: Jesse Harris Building
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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
Investigators
- Principal Investigator: Hollie Raynor, PhD, University of Tennessee-Knoxville
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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.
Clinical Trials on Overweight
-
University Hospital, LilleNational Research Agency, France; European Union; University of Lille Nord de... and other collaboratorsNot yet recruitingOverweight and Obesity | Overweight, Childhood | Overweight, Infant
-
Children's Hospital Los AngelesUniversity of Southern California; Tufts Medical CenterRecruitingOverweight and Obesity | Overweight AdolescentsUnited States
-
University of AarhusThe Danish Dairy Research Foundation, Denmark; Sygekassernes HelsefondCompletedOverweight and Obesity | Overweight Adolescents | Metabolic DiseaseDenmark
-
Memorial Sloan Kettering Cancer CenterRecruitingObesity | Overweight | Overweight and Obesity | Obese | Overweight or ObesityUnited States
-
University Hospital Bispebjerg and FrederiksbergUniversity of CopenhagenCompleted
-
Holbaek SygehusUniversity of Copenhagen; University of Florida; University of Minnesota; Hebrew... and other collaboratorsRecruitingChildhood Overweight and ObesityDenmark
-
Khyber Medical University PeshawarRecruitingObesity, OverweightPakistan
-
National Taiwan University HospitalCompleted
-
Institut Investigacio Sanitaria Pere VirgiliCompletedObesity, Childhood | Overweight and Obesity | Overweight, ChildhoodSpain
-
Children's Hospital SrebrnjakBelupo; Podravka d.d.RecruitingBody Weight | Overweight and ObesityCroatia