- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02928913
The Associations Between Sedentary Behaviour and Impact Characteristics on Bone Health
Study Overview
Detailed Description
Significant proportions of adults engage in sedentary behaviour for prolonged periods of time which is generally regarded as having deleterious effects on health. However, far less is known about its specific effects on bone health. Exercise has been proposed as a method of improving bone health, as impact forces generated as the foot contacts the ground during physical activity have the potential to aid bone maintenance and development.
The properties of bone are regulated through the amount mechanical loading, frequency of loading and duration of loading endured, which can create an osteogenic effect. These variables can be quantified via accelerometry which records the magnitude, rate and duration of accelerations experienced at the site on the body where the accelerometer is worn. Although there is a vast amount of literature where accelerometers have been used to monitor physical activity, there is a lack of studies that use accelerometers to determine the most effective exercise for bone, especially in relation to the lumbar spine. Exploring the bone health and loading characteristics of sedentary and low and highly active non-sedentary individuals will provide evidence upon which to base future interventions that are likely to be of benefit for bone health in sedentary populations.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
West Midlands
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Walsall, West Midlands, United Kingdom, WS1 3BD
- University of Wolverhampton
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Male or female aged 30 - 60 years Individuals who are sedentary and do not participate in physical activities Individuals who participate in some physical activities Individuals who are highly active Must be free from injury or illness that will affects following typical weekly routines.
Exclusion Criteria:
Any medical condition that affects bone health, e.g. osteoporosis. Currently takes medication that affects bone health, e.g. long term steroid use.
Inability to participate in typical daily activity, e.g. severe arthritis, injury. Women who are post menopause Women who are on hormone replacement therapy Unable to participate in DXA scan, e.g. due to recent exposure to radiation, pregnancy status.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Sedentary
Predominantly engage in sedentary behaviours
|
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Non-sedentary
Predominantly engage in non-sedentary behaviours
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Bone mineral density
Time Frame: One day
|
One day
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Mechanical loading dose during daily activity via accelerometry
Time Frame: 7 days
|
7 days
|
Mechanical loading intensity during daily activity via accelerometry
Time Frame: 7 days
|
7 days
|
Functional movement assessment: Grip Strength
Time Frame: One day
|
One day
|
Functional movement assessment: Timed up and go
Time Frame: One day
|
One day
|
Functional movement assessment: 10m walk test
Time Frame: One day
|
One day
|
Functional movement assessment: 5 times sit to stand
Time Frame: One day
|
One day
|
Functional movement assessment: gait analysis (acceleration at hip and lumbar spine)
Time Frame: One day
|
One day
|
Functional movement assessment: gait analysis (ground reaction force)
Time Frame: One day
|
One day
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 01/0416/TS/UOW
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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