Dementia Clinical Trial
Official title:
Exercise & Health Promotion for MCI: A Controlled Trial
Verified date | October 2012 |
Source | University of Washington |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
The purpose of this project is to evaluate an exercise and health promotion program for older adults with mild memory loss. The study will investigate the efficacy of a memory-enhanced exercise and health promotion program to determine whether it is more effective than a social walking program in delaying further memory decline, improving mood and physical function, and enhancing quality of life.
Status | Completed |
Enrollment | 181 |
Est. completion date | October 2012 |
Est. primary completion date | October 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 70 Years and older |
Eligibility |
Inclusion Criteria: - Mild Cognitive Impairment defined as - - Memory complaint - - Objective memory impairment for age and education - - Largely intact general cognitive function - - Essentially preserved activities of daily living - - Not already diagnosed with dementia - Insufficient physical activity defined as less than 150 minutes per week of moderate intensity physical activity - Not currently in an exercise program similar to the study program Exclusion Criteria: - Not ambulatory - Expected to move from the study geographic area during the study period - Have a known terminal illness - Actively suicidal, hallucinating, or delusional - Hospitalized for a psychiatric disorder in the 12 months before baseline - Uncontrolled chronic conditions, e.g. uncontrolled hypertension, unstable angina, uncontrolled blood glucose - Blind or deaf |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Northwest Research Group on Aging, Department of Psychosocial and Community Health, University of Washington School of Nursing | Seattle | Washington |
Lead Sponsor | Collaborator |
---|---|
University of Washington |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in cognitive status | baseline, 3, 6, 12, 18, 24, 30, and 36 months | No | |
Secondary | Changes in health, affective, and functional status | baseline, 3, 6, 12, 18, 24, 30, and 36 months | No |
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