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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02485197
Other study ID # 12-1029-F6A
Secondary ID
Status Completed
Phase N/A
First received April 25, 2013
Last updated March 15, 2017
Start date March 2013
Est. completion date June 2015

Study information

Verified date March 2017
Source University of Kentucky
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a small pilot aerobic training trial designed to examine differences between normal-high and low vitamin D levels and 7-days of aerobic training on local VO2 measured by non-invasive Hybrid Diffuse Optical Spectroscopy.


Recruitment information / eligibility

Status Completed
Enrollment 7
Est. completion date June 2015
Est. primary completion date October 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years to 75 Years
Eligibility Inclusion Criteria:

- 65-75 years of age

Exclusion Criteria:

- Currently have or have a history of cardiovascular or pulmonary disease that would preclude the involvement in the performance of exercise.

- Uncontrolled diabetes or hypertension.

- History of neurological conditions related to spinal derangement, disk disease, peripheral neuropathies, tremor and rigidity

- History of leg/hip trauma, inflammation, infection rhabdomyolysis, or leg surgery in the past 3 months

- Have a diagnosis of osteoporosis (as determined by DXA)

- Participated in a resistance or aerobic training program in the last 3 months

- Engage in more than 1 hr/week of vigorous activity

- Body mass index >29

- On hormone replacement therapy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
7 continuous days of aerobic training
For 7 consecutive days, subjects will perform up to 45 minutes of exercise consisting of treadmill walking at a progressive intensity of about 60-65% of their maximum heart rate. This heart rate range is estimated to be below 60% VO2 max.

Locations

Country Name City State
United States University of Kentucky Lexington Kentucky

Sponsors (1)

Lead Sponsor Collaborator
David Travis Thomas

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle VO2 consumption The objective is to examine the difference in gastrocnemius VO2 consumption in individuals that either have normal-high or low 25(OH)D and are undergoing 7-days of a treadmill training program. Up to 3 months
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