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Clinical Trials/NCT00714506
NCT00714506
Completed
Not Applicable

Effects of a Weight Reduction and Lifestyle Program in Older Adults

University of Pittsburgh1 site in 1 country36 target enrollmentMarch 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Functional Disability
Sponsor
University of Pittsburgh
Enrollment
36
Locations
1
Primary Endpoint
time to walk 400 m
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

This research study will assess the effects of two different programs on weight, body composition, mobility and improved health. Measures of health will include functional abilities, and physical performance. The 2 programs being tested will be provided the same physical activity program which will include aerobic activity and resistance (weight) training. The intervention study will last up to 1 year with follow-up at 6 months and yearly phone calls thereafter.

Registry
clinicaltrials.gov
Start Date
March 2008
End Date
December 2009
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Anne B. Newman

Professor of Epidemiology

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • Age 65 and older
  • BMI 28 to 39.9
  • Sedentary lifestyle defined by formal exercise less than 3 times per week for a total of less than 90 minutes.
  • Self report of ability to walk ¼ mile (2-3 blocks)
  • Ability to complete the 400 meter walk without a cane or walker in less than 15 minutes
  • Successful completion of the behavioral run-in phase which includes an activity log and a food diary
  • Willingness to be randomized to either intervention group
  • Willingness to attend meetings and physical activity sessions in McKeesport

Exclusion Criteria

  • Diabetes requiring insulin, history of diabetic coma, or diabetes out of control defined as fasting blood sugar greater than 300
  • Severe hypertension, e.g. SBP\> 180, DBP \> 100
  • Failure to provide informed consent
  • Nursing home resident or resident in a facility where they have no control over food choices
  • Significant cognitive impairment, defined as a known diagnosis of dementia or a 3MSE Cognitive Function score \< 80
  • Major psychiatric disorder
  • Unable to communicate because of severe hearing loss or speech disorder
  • Severe visual impairment
  • Celiac sprue or other malabsorption syndromes
  • Consume more than 5 alcoholic drinks per day, or more than 15 drinks per week

Outcomes

Primary Outcomes

time to walk 400 m

Time Frame: at 6 mo intervals

Secondary Outcomes

  • weight loss(6 month intervals)

Study Sites (1)

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