Elderly, Frail Clinical Trial
Official title:
Evaluation of the Effect of a 4-Month Intervention of Exercise and/or Vitamin D on Mobility Function and Strength in Frail Elderly Subjects
Verified date | January 2009 |
Source | Pfizer |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The study will explore multiple mobility function tests as well as functional and neuropsychological tests in elderly subjects at risk for falls and disability, before and after 4-month exercise and/or Vitamin D intervention.
Status | Terminated |
Enrollment | 64 |
Est. completion date | January 2008 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 75 Years and older |
Eligibility |
Inclusion Criteria: - Elderly subjects with moderate frailty residing in assisted living facilities. Exclusion Criteria: - Presence of progressive, unstable chronic disease; hyperparathyroidism, hypercalcemia. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Pfizer Investigational Site | Farmington | Connecticut |
United States | Pfizer Investigational Site | Hyattsville | Maryland |
United States | Pfizer Investigational Site | New York | New York |
United States | Pfizer Investigational Site | Roslindale | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Pfizer |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Characterization of effect of 4-month exercise and/or Vitamin D intervention on mobility function and strength in frail elderly subjects. | Throughout trial | No | |
Secondary | Evaluation of utility and variability of mobility function tests and biomarkers, as well as explore the predictors for the exercise and/or Vitamin D intervention response in frail elderly subjects. | throughout trial | No |
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