Steps Toward Adapting Physical Activity Guidelines for the Lower Mississippi Delta Population (STEPS)
This study has been completed.
Sponsor:
Pennington Biomedical Research Center
Collaborator:
USDA Beltsville Human Nutrition Research Center
Information provided by:
Pennington Biomedical Research Center
ClinicalTrials.gov Identifier:
NCT01264757
First received: December 3, 2010
Last updated: December 20, 2010
Last verified: December 2010
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
This feasibility study specifically addresses the issue of adapting US dietary guidelines physical activity recommendations to the population of the Lower Mississippi Delta. The hypothesis is that including a pedometer as a self-monitoring tool as part of adapted physical activity guidelines will result in greater immediate increases in physical activity (as monitored by an accelerometer) than an education program alone.
| Condition | Intervention | Phase |
|---|---|---|
|
Physical Inactivity |
Behavioral: Physical Activity Educational Materials Behavioral: Pedometer |
Phase 0 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Steps Toward Adapting Physical Activity Guidelines for the Lower Mississippi Delta Population |
Resource links provided by NLM:
Further study details as provided by Pennington Biomedical Research Center:
Primary Outcome Measures:
- Minutes spent in moderate-to-vigorous physical activity (MVPA) [ Time Frame: The primary outcome is measured at baseline and after a 7-day intervention period (1 week) ] [ Designated as safety issue: No ]A GT3X accelerometer is used to monitor each participants physical activity levels for seven consecutive days at baseline and again following a 7-day intervention period. The amount of time per day spent above a threshold of 2200 accelerometer counts/min is averaged over at least three days as the measure of MVPA.
| Enrollment: | 43 |
| Study Start Date: | February 2010 |
| Study Completion Date: | June 2010 |
| Primary Completion Date: | June 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Education
Educational brochure about physical activity provided.
|
Behavioral: Physical Activity Educational Materials
A brochure was provided to participants about the health benefits of physical activity and physical activity recommendations
|
|
Experimental: Pedometer
A pedometer was provided in addition to educational materials.
|
Behavioral: Pedometer
A pedometer was provided to participants in addition to educational materials about the health benefits of physical activity.
|
Detailed Description:
The purpose of this study was to determine if a short-term pedometer-based intervention results in immediate increases in time spent in moderate-to-vigorous physical activity (MVPA) compared to a minimal educational intervention.A sample of 43 overweight adults 35 to 64 years of age participated in a one week pedometer-based feasibility trial monitored by accelerometry. Participants were randomized into a one-week education-only group or a group that also wore a pedometer. Accelerometer-measured MVPA was measured over 7 days at baseline and post-intervention.
Eligibility| Ages Eligible for Study: | 35 Years to 64 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- 35 to 64 years of age
- body mass index (BMI) between 25 and 34.9 kg/m2
- being able to walk without limitation
Exclusion Criteria:
- cardiovascular, respiratory, gastrointestinal, neuromuscular, neurological, or psychiatric problems; musculoskeletal problems interfering with exercise
- immunodeficiency problems
- malignancies in the last 5 years
- any other medical condition or life threatening disease that could be aggravated by exercise
Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study.
To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01264757
Please refer to this study by its ClinicalTrials.gov identifier: NCT01264757
Locations
| United States, Louisiana | |
| Pennington Biomedical Research Center | |
| Baton Rouge, Louisiana, United States, 70808 | |
Sponsors and Collaborators
Pennington Biomedical Research Center
USDA Beltsville Human Nutrition Research Center
Investigators
| Principal Investigator: | Peter T Katzmarzyk, PhD | Pennington Biomedical Research Center |
More Information
No publications provided by Pennington Biomedical Research Center
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Peter T. Katzmarzyk, Pennington Biomedical Research Center |
| ClinicalTrials.gov Identifier: | NCT01264757 History of Changes |
| Other Study ID Numbers: | PBRC29034 |
| Study First Received: | December 3, 2010 |
| Last Updated: | December 20, 2010 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Pennington Biomedical Research Center:
|
pedometer accelerometer moderate-to-vigorous physical activity adult randomized trial |
ClinicalTrials.gov processed this record on March 01, 2015