- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03218605
Which Physical Activity Influences Achilles Tendon Blood Flow the Most?
November 30, 2021 updated by: University Ghent
Effect of Warming-up Activities on the Vascularisation of the Achilles Tendon: a Cohort Study
Previous studies have shown that a decreased blood flow is a risk factor in the occurrence of Achilles tendon (AT) injuries.
Based on the current literature, no consensus was reached as to the most solid warming-up of the AT.
Therefore, knowledge about activities which increase blood flow in the AT could be useful in the development of a solid warming-up programme for the AT.
The aim of this investigation was to define the influence of different kinds of physical activity on the vascularisation of the AT in a healthy asymptomatic population.
Subjects performed five activities in randomized order: running, static stretch, dynamic stretch, cycling and rope skipping.
The vascularisation of the AT of the dominant limb was measured with the non-invasive oxygen-to-see (O2C) device.
Blood flow was measured before, immediately after, five and ten minutes after activity to investigate the duration of the vascular response to activity.
Study Overview
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
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
-
-
-
Ghent, Belgium
- Ghent University
-
-
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
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- no history of Achilles tendon complaints
- healthy and active adolescents
Exclusion Criteria:
- history of Achilles tendon pain or current complaints
- not healthy or not active population
- children
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
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: healthy active participants
|
Subjects performed five activities: running, static stretch, dynamic stretch, cycling and rope skipping
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Achilles tendon blood flow
Time Frame: 3 minutes before and immediately (0 minutes) after the physical activity to assess the change in blood flow due to the physical activity
|
measured with the non-invasive O2C device
|
3 minutes before and immediately (0 minutes) after the physical activity to assess the change in blood flow due to the physical activity
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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 (Actual)
March 1, 2014
Primary Completion (Actual)
January 1, 2018
Study Completion (Actual)
January 1, 2018
Study Registration Dates
First Submitted
July 5, 2017
First Submitted That Met QC Criteria
July 13, 2017
First Posted (Actual)
July 14, 2017
Study Record Updates
Last Update Posted (Actual)
December 1, 2021
Last Update Submitted That Met QC Criteria
November 30, 2021
Last Verified
November 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 2013/401
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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