- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05925244
The Anabolic and Catabolic Effect of Loaded and Unloaded Exercise on Articular Cartilage Health
June 28, 2023 updated by: University of Manitoba
A Preliminary Study on the Effect of Loaded and Unloaded Exercise on Anabolic and Turnover Activity of Articular Cartilage in Healthy Young Adults
The serum concentration of cartilage oligomeric matrix protein (sCOMP) has been considered a mechano-sensitive biomarker of articular cartilage turnover, and N-propeptide of type II collagen (PIIANP) is a proposed biomarker of type II collagen synthesis.
Few studies have investigated both the anabolic and turnover response of articular cartilage as a result of acute changes in body weight mass during exercise.
Using a repeated measures cross-over design, fifteen healthy adults (age 18-30 years) performed three, 30-minute bouts of treadmill walking exercise under 3 loading conditions: (1) control (no alteration to body mass); (2) loaded (12% increase in body mass using a weighted vest); and (3) unloaded (12% decrease in body mass using lower body positive pressure).
Venous blood was collected before, immediately after, and 15 and 30 minutes after exercise to investigate cartilage turnover (sCOMP) and anabolism (PIIANP).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
15
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
-
-
Manitoba
-
Winnipeg, Manitoba, Canada, R3T 2N2
- University of Manitoba
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Healthy
- 18-30 years old
Exclusion Criteria:
- Traumatic injury to the lower extremity in the past year
- Hip, knee, or ankle surgery
- Radiographic evidence of joint degeneration
- Cardiovascular disease
- Ankylosing spondylitis
- Psoriatic arthritis
- Chronic reactive arthritis
- Renal problems requiring peritoneal dialysis or hemodialysis
- Not currently using any prescription or non-prescription medications and/or nutritional supplements
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: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Control
The control condition did 30 minutes of walking exercise with their own body mass.
|
Control (no alteration to body mass).
|
|
Experimental: +12% Body Mass
The +12% body mass condition did 30 minutes of walking exercise wearing a weighted vest with +12% of their body mass applied.
|
Loaded walking exercise (12% increase in body mass using a weighted vest).
|
|
Experimental: -12% Body Mass
The -12% body mass condition did 30 minutes of walking exercise using a lower body positive pressure treadmill with -12% of their body mass applied.
|
Unloaded walking exercise (12% decrease in body mass using lower body positive pressure).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Serum cartilage oligomeric matrix protein (sCOMP)
Time Frame: sCOMP was measured at baseline, immediately post, and 15- and 30-minutes post exercise.
|
The systemic blood serum concentration of sCOMP was evaluated in all participants under the 3 conditions in a crossover trial.
|
sCOMP was measured at baseline, immediately post, and 15- and 30-minutes post exercise.
|
|
N-propeptide of type II collagen (PIIANP)
Time Frame: PIIANP was measured at baseline, immediately post, and 15- and 30-minutes post exercise.
|
The systemic blood serum concentration of PIIANP was evaluated in all participants under the 3 conditions in a crossover trial.
|
PIIANP was measured at baseline, immediately post, and 15- and 30-minutes post exercise.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Stephen M Cornish, PhD, University of Manitoba
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)
September 27, 2019
Primary Completion (Actual)
March 1, 2020
Study Completion (Actual)
March 1, 2020
Study Registration Dates
First Submitted
June 21, 2023
First Submitted That Met QC Criteria
June 21, 2023
First Posted (Actual)
June 29, 2023
Study Record Updates
Last Update Posted (Actual)
July 3, 2023
Last Update Submitted That Met QC Criteria
June 28, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- HS22322
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The data will not be available to other researchers as we do not have ethical approval to do so.
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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