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OpenTrials
Completed

NCT Number: NCT00164515

Increasing Physical Activity Among Overweight Women With Mobility Disabilities.

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

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Illinois, Chicago

Chicago, Illinois, 60612, United States

About this study

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).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Personalized exercise programme (PEP)

Behavioral

Physician referred overweight and obese clients to 24 month personalized exercise programme at the U. of Illinois, Chicago

Other names: PEP

Primary outcomes

  1. 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).

  2. Body mass index (BMI)

    Time frame: 24 months

    Derived emperically

  3. Blood lipids

    Time frame: 24 months

    Derived emperically

  4. Weight

    Time frame: 24 months

    Derived emperically

  5. Blood Pressure

    Time frame: 24 months

    Dervied emperically

Secondary outcomes

  1. Psychosocial Health

    Time frame: 24 months

    Confirmed using the Quality of Wellbeing scale (Anderson et al 1989), and CARDIA-2 scale, an 11-item assessment (Allen et al 2001).

Sponsors and collaborators

Lead sponsor

Centers for Disease Control and Prevention

Fed

Collaborators

  • University of Illinois, Center on Health Promotion Research for Persons with Disabilities

Registry information

Official study title

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

Acronym: PEP

Important dates

Study start
2004
Primary completion
2007
Study completion
2007
First posted
Sep 14, 2005
Registry last updated
Jul 26, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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