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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00596089
Other study ID # 2007-0274
Secondary ID
Status Completed
Phase N/A
First received January 7, 2008
Last updated October 1, 2015
Start date October 2007
Est. completion date March 2008

Study information

Verified date January 2008
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Decline in muscle function may increase risk of hip fracture and decrease quality of life. Different tests are currently used to measure muscle function but they do not work for all individuals. A test called "jumping mechanography," which measures jumping power, may be useful in more people and obtain better information. This study will help us determine whether this test is able to detect differences between muscle function in younger and older adults, as well as whether it is a safe method to use in all ages.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date March 2008
Est. primary completion date March 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

1. Women and men aged 20 to 30 or = 60 years

2. Able and willing to sign informed consent.

3. Ability to stand without assistance.

Exclusion Criteria:

1. Acute pain different and/or worse than the individuals chronic baseline pain

2. History of recent trauma to musculoskeletal system

3. Neuromuscular disease impairing balance to the degree of not being able to stand without assistance.

4. History of fragility fracture within the last year

5. Patients with a BMD T-score of less than -3.5 at any measured site and a vertebral fracture.

6. History of severe end-organ disease, e.g., cardiovascular, hepatic, hematologic, pulmonary, etc., which might limit the ability to complete this study.

7. Recent history of malignancy with metastasis to the musculoskeletal system.

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Wisconsin Osteoporosis Clinical and Research Program Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The primary outcome is the instantaneous weight corrected peak power taken from the maximal countermovement jump single session No
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