Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01740661
Other study ID # IS-HPL-01
Secondary ID
Status Completed
Phase N/A
First received November 20, 2012
Last updated April 15, 2014
Start date November 2012
Est. completion date January 2013

Study information

Verified date January 2013
Source University of Calgary
Contact n/a
Is FDA regulated No
Health authority Canada: Canadian Institutes of Health Research
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the immediate effects of cryotherapy on the lower extremity biomechanics during running.


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.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date January 2013
Est. primary completion date December 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 40 Years
Eligibility 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 Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
Cryotherapy
The subjects will be exposed to a cold (~ 12° C) water immersion tub at the umbilical level for 20 minutes.
Control
The subjects will be exposed to a non-cold (~ 26° C) water immersion tub at the umbilical level for 20 minutes.

Locations

Country Name City State
Canada Human Performance Laboratory, University of Calgary Calgary Alberta

Sponsors (1)

Lead Sponsor Collaborator
University of Calgary

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Knee frontal plane moments 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 No
See also
  Status Clinical Trial Phase
Completed NCT05071469 - Comparison of Two Different Treatment Methods N/A
Completed NCT02597959 - Reducing Musculoskeletal Stresses and Work-related Injuries Among Allied Health Professionals in Surgical Care N/A
Completed NCT04009369 - Impacts of Physiotherapy Services in a Quebec Emergency Department N/A
Not yet recruiting NCT05356598 - Help-seeking Intentions of ROTC Trainees N/A
Recruiting NCT04850222 - Fluoxetine Mitigation Mental Health Study for Patients With Musculoskeletal Trauma Early Phase 1
Completed NCT05254470 - Real-World Experience of Patients Treated for Musculoskeletal Injuries With SAM in Routine Care
Completed NCT03063814 - Effects of App-based Versus Personal On-site Instruction on Neuromuscular Activity in Injury Prevention Exercises N/A
Recruiting NCT06074783 - A Study of Human Allogeneic Bone-marrow Derived Mesenchymal Stromal Cell Product (StromaForte) in Patients With Musculoskeletal Injuries and/or Degeneration Phase 1/Phase 2
Recruiting NCT05122728 - Post-Concussion Musculoskeletal Injury Risks
Recruiting NCT05596162 - The Effect of Low-Intensity Blood Flow Restriction Therapy on the Management of Acute Ankle Sprains N/A
Completed NCT04199572 - Synergistic Effect Of Parenteral Diclofenac And Paracetamol In The Pain Management Of Acute Limb Injuries Phase 4
Completed NCT05550610 - Evaluation of Mindfulness and Yoga in Basic Combat Training N/A
Recruiting NCT05473208 - Lumbar Assistive Exoskeletons in Caregiving N/A
Completed NCT04796753 - Detection of Neuromuscular Deficits in Uninjured Youth Basketball Players
Recruiting NCT04800484 - The Effects of AFO Heel Height and Stiffness on Gait N/A
Not yet recruiting NCT04632563 - Prevalence of Musculoskeletal Symptoms in the Cambridge NIHR BioResource
Terminated NCT03850470 - The Diagnostic Accuracy of the Clinical Examination
Recruiting NCT05110729 - Quality of Life and Life Satisfaction in Pediatric and Adolescent Gymnasts Through Injury
Completed NCT05370872 - Efficacy of a Remotely Administered Functional Capacity Test on Return-to-work Outcomes N/A
Recruiting NCT05780502 - Use of an Integrated Orthotic and Rehabilitation Initiative for Treatment of Lower Extremity Musculoskeletal Disorders