- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01740661
Cryotherapy and Joint Biomechanics During Running
April 15, 2014 updated by: Claudiane Fukuchi, University of Calgary
Effects of Cryotherapy on Lower Extremity Joint Biomechanics During Running in Healthy Adults
The purpose of this study is to determine the immediate effects of cryotherapy on the lower extremity biomechanics during running.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Cryotherapy or cold therapy has widely been used as a treatment modality in both acute and chronic injuries.
It is believe that the application of cryotherapy can help to decrease pain, muscle soreness, soft tissue swelling, and cause vasoconstriction of blood vessels reducing heat loss.
The nerve conduction velocity and muscle-spindle firing rate also decreases with cryotherapy, which results in changes in proprioception acuity.
Cryotherapy has also been used prior to exercise (pre-cooling) to improve endurance activities.
However, given the possible detrimental effects of cryotherapy on proprioception acuity, the use of this treatment modality prior to exercise could pose an increased risk of musculoskeletal injury.
The effects of cryotherapy on lower extremity biomechanics during athletic movements is poorly understood despite the wide use among physiotherapists, athletic therapists and clinicians.
Therefore, the purpose of this investigation is to determine the effects of cold water immersion on lower extremity biomechanics during running.
The investigators hypothesize that cryotherapy as a form of treatment can increase the load in the lower extremity joint during gait biomechanics.
Study Type
Interventional
Enrollment (Actual)
26
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
-
-
Alberta
-
Calgary, Alberta, Canada, T2N 1N4
- Human Performance Laboratory, University of Calgary
-
-
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 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- males or females (18 - 40 yrs)
- no injuries of the lower extremity in the past 6 months prior to participation
- recreationally active
- in good health upon entry into the study
- willing to volunteer for the present project.
Exclusion Criteria:
- lower extremity injury within the last 6 months
- circulatory, vestibular or any contradiction to cryotherapy including Raynaud's disease
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: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Cryotherapy
The subjects will be exposed to a cold (~ 12° C) water immersion tub at the umbilical level for 20 minutes.
|
The subjects will be exposed to a cold (~ 12° C) water immersion tub at the umbilical level for 20 minutes.
|
|
Placebo Comparator: Control
The subjects will be exposed to a non-cold (~ 26° C) water immersion tub at the umbilical level for 20 minutes.
|
The subjects will be exposed to a non-cold (~ 26° C) water immersion tub at the umbilical level for 20 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee frontal plane moments
Time Frame: 20 minutes
|
Knee frontal plane loading will be calculated using inverse dynamics based on the ground reaction force data from a force plate and with kinematic data recorded by high speed cameras.
Kinematics and kinetics data will be taken during running at 4m/s from each participant prior and after the intervention.
|
20 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
November 1, 2012
Primary Completion (Actual)
December 1, 2012
Study Completion (Actual)
January 1, 2013
Study Registration Dates
First Submitted
November 20, 2012
First Submitted That Met QC Criteria
November 29, 2012
First Posted (Estimate)
December 4, 2012
Study Record Updates
Last Update Posted (Estimate)
April 16, 2014
Last Update Submitted That Met QC Criteria
April 15, 2014
Last Verified
January 1, 2013
More Information
Terms related to this study
Other Study ID Numbers
- IS-HPL-01
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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