Use of Jumping Mechanography as a Method to Assess Musculoskeletal Status in Older Adults

October 1, 2015 updated by: University of Wisconsin, Madison

Use of Jumping Mechanography as a Method to Assess Musculoskeletal Status in Older Adults: A Pilot Study

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.

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Anticipated)

80

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Wisconsin
      • Madison, Wisconsin, United States, 53705
        • University of Wisconsin Osteoporosis Clinical and Research Program

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Men and women 60 years and older and men and women 20-30 years of age

Description

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
1
Men and women 60 years and older
2
Men and women 20-30 years of age

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
The primary outcome is the instantaneous weight corrected peak power taken from the maximal countermovement jump
Time Frame: single session
single session

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Neil C Binkley, MD, University of Wisconsin - Institute on Aging

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2007

Primary Completion (Actual)

March 1, 2008

Study Completion (Actual)

March 1, 2008

Study Registration Dates

First Submitted

January 7, 2008

First Submitted That Met QC Criteria

January 15, 2008

First Posted (Estimate)

January 16, 2008

Study Record Updates

Last Update Posted (Estimate)

October 5, 2015

Last Update Submitted That Met QC Criteria

October 1, 2015

Last Verified

January 1, 2008

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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