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Steps Toward Adapting Physical Activity Guidelines for the Lower Mississippi Delta Population

Steps Toward Adapting Physical Activity Guidelines for the Lower Mississippi Delta Population

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01264757
Acronym
STEPS
Enrollment
43
Registered
2010-12-22
Start date
2010-02-28
Completion date
2010-06-30
Last updated
2016-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Inactivity

Keywords

pedometer, accelerometer, moderate-to-vigorous physical activity, adult, randomized trial

Brief summary

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.

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.

Interventions

BEHAVIORALPhysical Activity Educational Materials

A brochure was provided to participants about the health benefits of physical activity and physical activity recommendations

BEHAVIORALPedometer

A pedometer was provided to participants in addition to educational materials about the health benefits of physical activity.

Sponsors

United States Department of Agriculture (USDA)
CollaboratorFED
Pennington Biomedical Research Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
35 Years to 64 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Minutes spent in moderate-to-vigorous physical activity (MVPA)The primary outcome is measured at baseline and after a 7-day intervention period (1 week)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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026