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Clinical Trials/NCT00164515
NCT00164515CompletedPhase 2

Personalized Exercise Programme (PEP) I: Physician Referral Approach to Increasing Awareness and Sustainability of Physical Activity for Overweight Adults With Mobility Limitations.

Centers for Disease Control and Prevention1 site in 1 country96 target enrollmentStarted: October 1, 2004Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
96
Locations
1
Primary Endpoint
Body mass index (BMI)

Study Overview

Brief Summary

This study aims to increase physical activity among overweight African-American women with mobility limitations.

Detailed Description

Regular, sustainable physical activity can have a dramatic effect on reducing obesity and other secondary conditions and increasing quality of life. People with mobility limitations have a higher level of physical inactivity resulting from numerous personal and environmental barriers to physical activity participation. This project will evaluate the feasibility of increasing physical activity among overweight individuals with mobility limitations through physician-referrals to a personalized exercise programme at the Chicago-based National Center on Physical Activity and Disability (NCPAD).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •18 years or older
  • •English speaking
  • •Self-reported mobility limitation
  • •BMI greater than or equal to 27
  • •Receiving care at the University of Illinois, Chicago (UIC) Medical Center
  • •Sedentary

Exclusion Criteria

  • •did not receive physician approval to participate

Arms & Interventions

Arm 1: Physical activity awareness

No Intervention

The awareness group received a physician-recommendation to exercise an informational brochure, and pedometer.

Arm 2: Lower Support

Experimental

The lower support group received arm 1 plus monthly newsletter, weekly personalized exercise support via telephone.

Intervention: Personalized exercise programme (PEP) (Behavioral)

Arm 3: Higher support

Experimental

The higher support group received arm 1 plus arm 2 plus a face-to-face monthly exercise support group.

Intervention: Personalized exercise programme (PEP) (Behavioral)

Outcomes

Primary Outcomes

Body mass index (BMI)

Time Frame: 24 months

Derived emperically

Physical activity

Time Frame: 24 months

Physical activity was assessed using the Physical Activity and Disability Scale (PADS), the Barriers to Physical Activity and Disbility Scale (B-PADS), (Rimmer et al 2000) and the Mobility Limitation score (Velozo et al 1999).

Blood Pressure

Time Frame: 24 months

Dervied emperically

Weight

Time Frame: 24 months

Derived emperically

Blood lipids

Time Frame: 24 months

Derived emperically

Secondary Outcomes

  • Psychosocial Health(24 months)

Investigators

Sponsor
Centers for Disease Control and Prevention
Sponsor Class
Fed
Responsible Party
Sponsor

Study Sites (1)

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