Status:
COMPLETED
Seniors Health and Activity Research Program-Pilot
Lead Sponsor:
Wake Forest University Health Sciences
Collaborating Sponsors:
National Institute on Aging (NIA)
Conditions:
Cognitive Function
Eligibility:
All Genders
70-85 years
Phase:
NA
Brief Summary
The purpose of this pilot study is to develop and conduct well-designed trial to assess whether a multi-factorial intervention involving physical activity and cognitive training reduces the risk of si...
Detailed Description
Evidence from small or uncontrolled studies indicates that physical exercise and cognitive training have considerable promise as prevention strategies, to the extent that they are often recommended; h...
Eligibility Criteria
Inclusion
- Age 70 to 85 years
- Summary score between 88 (80 for less than 8 years of education) and 95 on the Modified Mini-Mental Exam
- Sedentary lifestyle, i.e., not actively participating in a formal exercise program within the past 3 months (defined as 30 minutes or more of formal exercise at least once a week; brisk walks will be considered formal exercise, leisurely walks will not)
- Fluency in standard American English (to limit staffing and translation costs in this pilot)
- Willingness to be randomized to any of the four intervention conditions
Exclusion
- Failure to provide the name of a personal physician
- Living in a nursing home; persons living in assisted or independent housing will not be excluded
- Unable to communicate because of severe hearing loss or speech disorder
- Severe visual impairment, which would preclude completion of the assessments and/or intervention
- Neurologic disease, e.g. Alzheimer's (or other types of dementia), stroke that required hospitalization, Parkinson's, multiple sclerosis, amyotrophic lateral sclerosis, or prior diagnosis of mild cognitive impairment (MCI)
- Abnormal functioning based on the modified Telephone Interview for Cognitive Status (less than 30)
- Positive screen for MCI or dementia
- Scores greater than or equal to 1.5 standard deviations below normal on memory and non-memory domain tests (speed of processing, and verbal fluency)
- Severe rheumatologic or orthopedic diseases, e.g., awaiting joint replacement, active inflammatory disease
- Terminal illness with life expectancy less than 8 months, as determined by a physician
- Severe pulmonary disease, e.g., on home oxygen or chronic steroids
- Severe cardiac disease, including New York Health Association Class III or IV congestive heart failure, clinically significant aortic stenosis, history of cardiac arrest which required resuscitation, use of a cardiac defibrillator, or uncontrolled angina
- Other significant co-morbid disease that would impair ability to participate in the exercise-based intervention, e.g. renal failure on hemodialysis, severe or acute psychiatric disorder (e.g. bipolar disorder or major depression, schizophrenia), excessive alcohol use (more than 14 drinks per wk); persons with managed depression (on stable dosage for at least 3 months) will not be excluded
- Baseline Geriatric Depression Scale score greater than 6
- Other significant factors that may affect the ability for cognitive training, including a history of head trauma resulting in a loss of consciousness, current use of benzodiazepines, hypnotic or anticholinergic agents, and current use of cognitive enhancing prescription or investigational medications (e.g., donepezil, selegiline, tacrine)
- Member of household is already enrolled
- Lives distant from the study site or is planning to move out of the area in next 3 years or leave the area for more than 3 months during the next year
- History of participation in a cognitive program in the last 2 years (includes research studies involving memory training)
- Myocardial infarction, coronary artery bypass graft, or valve replacement within past 6 months
- Serious conduction disorder (e.g., 3rd degree heart block), uncontrolled arrhythmia
- Pulmonary embolism or deep venous thrombosis within past 6 months
- Stroke, hip fracture, hip or knee replacement, or spinal surgery within past 4 months
- Receiving physical therapy for gait, balance, or other lower extremity training
- Severe hypertension, e.g., systolic blood pressure over 160 mmHg, diastolic blood pressure over 110 mmHg
- Other temporary intervening events, such as sick spouse, bereavement, or recent move
- Participation in another intervention trial; participation in an observational study may be permitted
- Inability to commit to intervention schedule requirements
Key Trial Info
Start Date :
May 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 30 2010
Estimated Enrollment :
73 Patients enrolled
Trial Details
Trial ID
NCT00688155
Start Date
May 1 2008
End Date
June 30 2010
Last Update
January 4 2018
Active Locations (1)
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1
Wake Forest University Health Sciences
Winston-Salem, North Carolina, United States, 27157