The Vitality, Independence, and Vigor in Elders Study I Clinical Trial
NCT ID: NCT01198886
Last Updated: 2015-05-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
121 participants
INTERVENTIONAL
2010-09-30
2014-05-31
Brief Summary
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\- The primary hypothesis is that over the 6-month intervention period subjects in the intervention group will realize significant improvements in lower extremity function compared to a control group.
Secondary objectives
To evaluate changes in nutritional status that result from the ENP.
\- The secondary hypothesis is that subjects in the intervention group will realize significant increases in circulating insulin-like growth factor-1 (IGF-1) and 25-hydroxy vitamin D (25(OH)D) and demonstrate improvements in nutritional status compared to a control group.
To evaluate changes in inflammatory status that result from the ENP.
\- Subjects in the ENP group will exhibit reduced concentrations of circulating interleukin-6 (IL-6) compared with the control group.
To evaluate changes in psychosocial factors that result from the ENP
* The related hypothesis is that over the 6-month intervention period subjects in the intervention group will increase exercise self-efficacy, intrinsic motivation to exercise, and satisfaction of psychological needs compared to a control group.
* Additionally it is hypothesized that subjects in the intervention group will realize improvements in mood and quality of life compared to a control group.
To assess the feasibility of conducting the Exercise-Nutrition Program in a senior housing facility setting.
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Detailed Description
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Main objective
* The primary objective of this study is to evaluate changes in functional status that result from the Exercise-Nutrition Program (ENP).
* The primary hypothesis is that over the 6-month intervention period subjects in the intervention group will realize significant improvements in lower extremity function compared to a control group.
Secondary objectives
The secondary objectives of the research project are:
* To evaluate changes in nutritional status that result from the ENP.
* The secondary hypothesis is that subjects in the intervention group will realize significant increases in circulating IGF-1 and 25-hydroxy vitamin D (25(OH)D) and demonstrate improvements in nutritional status compared to the control group.
* Subjects in the ENP will exhibit reductions in circulating plasma IL-6 concentrations, which are indicative of systemic inflammatory status.
* To evaluate changes in psychosocial factors that result from the ENP.
* The related hypothesis is that over the 6-month intervention period subjects in the intervention group will increase exercise self-efficacy, intrinsic motivation to exercise, and satisfaction of psychological needs compared to a control group.
* Additionally it is hypothesized that subjects in the intervention group will realize improvements in mood and quality of life compared to a control group.
Another major objective is to assess the feasibility of conducting the Exercise-Nutrition Program in a senior housing center facility setting.
TRIAL DESIGN
Type of trial The study objectives will be achieved in the context of a controlled, randomized field trial. Randomization will be by site (senior housing center). Intervention group subjects will participate in the Exercise-Nutrition Program (ENP). Control group subjects will participate in the Successful Aging Program (SAP), which will provide them with useful skills and an adequate attention control, but will not affect the primary outcome of this study.
Subjects, groups and centers:
In each study group the number of subjects to complete the study protocol will be 40 (see also 9.3 statistical section). Assuming a conservative dropout rate of 10% after the 3 month intervention and 15% at the end of the 6 month study, a sample of 53 subjects per group, or 106 total, will be required to be enrolled in the study. 16-20- senior housing centers will be recruited and each will run one class with an average size of at least 5 subjects (maximum 25 subjects).
Sites will be assigned to one of 2 groups:
Group 1: Exercise-Nutrition Program (ENP) Group 2: Successful Aging Program (SAP)
Duration of subject participation:
Subjects will undergo the proposed intervention for 6 months. The target population for this study will be elderly people (65 yrs+) living in senior housing centers.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SINGLE
Study Groups
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Successful Aging Program
Successful Aging Program
Once per week discussion on lifestyle topics important to older adults. Classes conclude with a gentle upper body stretching routine.
Exercise-Nutrition Program
Exercise-Nutrition Program
Targeted exercise program offered 3-days per week at the study participants place of residence (senior housing facility). Other means to encourage physical activity outside of these exercise classes will be available. A nutrient-rich protein carbohydrate experimental beverage will be taken following the exercise sessions.
Interventions
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Successful Aging Program
Once per week discussion on lifestyle topics important to older adults. Classes conclude with a gentle upper body stretching routine.
Exercise-Nutrition Program
Targeted exercise program offered 3-days per week at the study participants place of residence (senior housing facility). Other means to encourage physical activity outside of these exercise classes will be available. A nutrient-rich protein carbohydrate experimental beverage will be taken following the exercise sessions.
Eligibility Criteria
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Inclusion Criteria
* Living at a senior housing facility
* SPPB score of 3-9
* BMI \<35
* 6CIT \< or = 14
* Permission of primary care provider
* Willingness to be randomized to either treatment group
Exclusion Criteria
* Participate in \>125 minutes per week of moderate to vigorous physical activity
* Moderate to severe cognitive impairment (6CIT \>15)
* Inability to communicate due to severe, uncorrectable hearing loss or speech disorder
* Severe visual impairment (if it precludes completion of assessments and/or intervention)
* Wheelchair bound
* Late-stage, progressive, degenerative neurologic disease, e.g., Parkinson's Disease, multiple sclerosis, acute lateral sclerosis.
* Severe rheumatologic or orthopedic diseases, e.g., awaiting joint replacement, active inflammatory disease
* Terminal illness with life expectancy less than 12 months, as determined by a physician
* Severe pulmonary disease, requiring either steroid pills or injections or the use of supplemental oxygen
* Severe cardiac disease, including NYHA Class III or IV congestive heart failure, clinically significant aortic stenosis, history of cardiac arrest, 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 psychiatric disorder (e.g. bipolar, schizophrenia), excessive alcohol use (\>14 drinks per wk); persons with depression will not be excluded
* Surgery in the previous 6 months
* Patient who cannot be expected to comply with treatment
* Inability to obtain signed authorization from participant's primary care health care provider.
65 Years
ALL
Yes
Sponsors
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Tufts University
OTHER
Responsible Party
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Principal Investigators
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Miriam E Nelson, PhD
Role: STUDY_DIRECTOR
Tufts University
Sara C. Folta, PhD
Role: PRINCIPAL_INVESTIGATOR
Tufts University
Roger F. Fielding, PhD
Role: PRINCIPAL_INVESTIGATOR
Tufts University
Locations
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Drake Village
Arlington, Massachusetts, United States
Nashoba Park
Ayer, Massachusetts, United States
Compass on the Bay
Boston, Massachusetts, United States
Chestnut Park at Cleveland Circle
Brighton, Massachusetts, United States
Neville Place at Fresh Pond
Cambridge, Massachusetts, United States
Youville House
Cambridge, Massachusetts, United States
Chelmsford Crossings
Chelmsford, Massachusetts, United States
Putnam Farms at Danvers
Danvers, Massachusetts, United States
Standish Village at Lower Mills
Dorchester, Massachusetts, United States
Youville Place
Lexington, Massachusetts, United States
Methuen Village
Methuen, Massachusetts, United States
Evans Park at Newton Center
Newton, Massachusetts, United States
Coleman House
Newton, Massachusetts, United States
The Falls at Cordingly Dam
Newton, Massachusetts, United States
Golda Meir House
Newton, Massachusetts, United States
Holland Street Center
Somerville, Massachusetts, United States
Waltham Crossings
Waltham, Massachusetts, United States
Countries
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References
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Corcoran MP, Chui KK, White DK, Reid KF, Kirn D, Nelson ME, Sacheck JM, Folta SC, Fielding RA. Accelerometer Assessment of Physical Activity and Its Association with Physical Function in Older Adults Residing at Assisted Care Facilities. J Nutr Health Aging. 2016;20(7):752-8. doi: 10.1007/s12603-015-0640-7.
Other Identifiers
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09.37.CLI
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
1006010
Identifier Type: -
Identifier Source: org_study_id
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