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Research History
| Title: |
Exercise and Recreation
for Individuals with a Disability: Assessment and Intervention
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| Funding Source:
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U.S. Department
of Education
National Institute on Disability and Rehabilitation Research (NIDRR)
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| Start Date:
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October 1, 1996
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| Length: |
36 months |
| Funding:
|
$525,000 |
| Description: |
This project demonstrates that participation in
exercise and physical activities improves function, facilitates
community reintegration, and enhances the quality of life of people
with disabilities. It:
- investigates the long-term effects of an exercise
fitness program on the physiology, metabolic performance, and
quality of life of people with spinal cord injury, stroke, and
cerebral palsy;
- examines the role of self-efficacy in maintaining
participation in an exercise fitness program;
- describes the types and frequency of recreation
and fitness activities among people who have had a stroke, people
with spinal cord injury, and people with cerebral palsy;
- examines the relationships between participation
in recreation and exercise programs and the health status, life
satisfaction, and depression in the above populations; and
- delineates barriers and deterrents to participation
in recreation and exercise programs that
exist for a variety of disability groups.
|
| Title:
|
Rehabilitation
Research and Training Center on Enhancing the Quality of Life of Stroke
Survivors: The Impact of Exercise and Education on the Quality of
Life of Stroke Survivors |
| Funding Source:
|
U.S. Department
of Education
National Institute on Disability and Rehabilitation Research (NIDRR)
|
| Start Date:
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October 1, 1998
|
| Length: |
5 years |
| Funding:
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$4,000,000
(Center for Health and Fitness: $403,000) |
| Description: |
This study will examine the effects of a sixteen week fitness training
program of aerobic training combined with and without resistance
training on a variety of physiological and psychological parameters.
The sixteen week intervention will consist of cardiovascular, strength,
and flexibility training. Pre- and post evaluations will be performed
for this time period for both psychologic and physiologic parameters.
A six month and a one year re-evaluation will also be performed.
Participation will be randomly assigned to one of the two groups.
The intention of this exercise intervention is to evaluate the different
modes of exercise on the physiologic parameters such as aerobic
capacity, blood lipid profile, body composition, range of motion
and muscular strength. Changes in functional capacity will also
be assessed through measures of ambulatory ability and changes in
energy expenditure. Specific exercise protocols will be designed
for participants with various levels of impairment. The duration
and intensity of each session will be incrementally increased throughout
the 16 weeks.
|
| Title: |
National
Center on Physical Activity and Disability |
| Funding Source: |
Centers for Disease Control and Prevention
|
| Start Date: |
April 1, 1999
|
| Length: |
48 months
|
| Funding: |
$3,000,000 (RIC Component: $600,000)
|
| Description: |
RIC's Center for Health and Fitness is collaborating with the University
of Illinois - Chicago for the development and operation of a national
information and resource center on physical activity for individuals
with disabilities.
|
| Title: |
Phase II Trial of Progressive Resistance
Training with Megesterol Acetate for the Treatment of Cancer-related
Weight Loss |
| Funding Source: |
Bristol-Meyers Squibb |
| Start Date: |
January 1, 1999
|
| Length: |
15 months; 3 Month Set-Up, 12 Months
Full Trial
|
| Funding: |
$175,000 (RIC Component: $46,000)
|
| Description: |
Currently, a joint effort between the RIC's Center for Health and
Fitness and the Northwestern Medical Oncology Department is conducting
a study related to the effects of the strength training on the fatigue
levels of terminal cancer patients in conjunction with taking an
appetite stimulant drug, Megesterol Acetate (MA). The strength training
program requires a 3 hour commitment per week for 12 weeks. This
trial will include 15 subjects over a one year period. In addition
to measuring fatigue levels of cancer patients, other evaluations
included in the study are body composition, maximal oxygen consumption
(VO2 max), one repetition maximum, and timed stair climbing.
|
| Title:
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Phase III Trial of Progressive
Resistance Training Versus Progressive Resistance Training Plus Procrit
for the Treatment of Cancer-related Fatigue |
| Funding Source: |
Ortho Biotech |
| Start Date:
|
January 1, 1999 |
| Length: |
15 Months; 3 Month Set-Up,
12 Months Full Trial |
| Funding:
|
$215,000 (RIC Component:
$43,000) |
| Description: |
RIC's Center for Health and Fitness and the Northwestern
Medical Oncology Department is conducting a second study to test
the effectiveness of the drug, Procrit. This study will investigate
the effects of a 12 week strength and cardiovascular training program
on fatigue levels of cancer patients taking Procrit. Procrit increases
erythropoietin and hemoglobin levels in patients suffering from
anemia exacerbated by chemotherapy and other cancer treatments.
In addition to measuring fatigue levels of 30 cancer subjects, body
composition, maximal oxygen consumption (VO2 max), one repetition
maximum, and timed stair climbing will be considered.
|
| Title: |
Home-Based Aerobic Conditioning for
Management of Symptoms of Fibromyalgia |
| Funding Source:
|
Pending |
| Start Date: |
|
| Length: |
8 Months; 2 Months Set-Up,
6 Months Full Trial |
| Funding:
|
|
| Description: |
The proposed study will examine the efficacy of a self-paced,
home-based aerobic conditioning program, with limited supervision,
for managing Fibromyalgia (FM). The study will further examine whether
symptom improvements are the result of objective changes in aerobic
conditioning as reflected in exercise testing. Patients will undergo
quantitative pressure algometry (to assess muscle tender points),
and will complete pain ratings and functional / psychological measures.
Data analysis will determine whether decreases in pain and other
symptoms of FM are associated with changes in conditioning as documented
by MET. Psychological measures will be tested as predictors of treatment
failure.
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