The Effect of Whole Body Cryotherapy on Recovery and Performance: a Randomized Controlled Trial (Cryotherapy)

This study investigates the effects of whole-body cryotherapy vs. cold-water immersion after a muscle damage protocol.

Study Overview

Status

Completed

Conditions

Detailed Description

In this study the effects of a single- or multiple whole body cryotherapy (-135°C for max. 2 minutes) vs. cold water immersion (10°C for 15 min) and a passive control group (20 min supine position) are compared. These effects are examined after a muscle damage protocol of the frontal thighs (3 x 30 jumps). The objective recovery parameters are vertical jump, maximum voluntary contraction of the anterior thigh muscle, heart rate, blood pressure, skin-core body temperature and the oxygen saturation of the thigh muscles. Subjective recovery parameters are the local muscle soreness details and the general exhaustion details. The parameters are directly and 24, 48 and measured 72 hours after exposure. The aim is to elicit the effects of whole body cooling to make recommendations to. The current scientific knowledge situation calls for further studies to whole body cooling.

Study Type

Interventional

Enrollment (Actual)

30

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

      • Landquart, Switzerland, 7302
        • Fachhochschule Südschweiz

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 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Only healthy young subjects 18-35 years no musculoskeletal surgery in trunk and lower extremities injury history in trunk and lower extremity for more than one year subjects taking anticonceptive medication are allowed to participate

Exclusion Criteria:

Actual injuries or injuries for less than one year in trunk and /or lower extremities injury history in trunk and lower extremity for more than one year with complaints anxiety of cooling subjects on medication pace maker cardiovascular disease pregnancy skeletal problems appendectomy for less than two years Morbus Raynaud syndrome

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Whole-body cryotherapy
The effects of whole-body cryotherapy (-135°C for 2 minutes) are investigated after a muscle damage protocol.
The whole body cryotherapy device is able to generatue temperatures up to -195°C for 3 minutes. In this study, we generate temperatures of -135°C for 2 minutes as proposed in the manual. The participant will enter the cabin in cold-resistant shoes and will remain in standing position during the whole procedure. The cold temperature is generated by vaporization of liquid nitrogen.
Other Names:
  • Cryomed s.r.o.
Other: Cold-water immersion
The effects of cold-water immersion (10°C for 15 minutes) are investigated after a muscle damage protocol.
The tub will be filled with cold water up to the sternal level of the participants. Adding ice will ensure a constant temperature. The participant will sit inside the tub during the whole procedure.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vertical Jump
Time Frame: 72 hours
Vertical Jump will be assessed in cm with the Just Jump Plate
72 hours
Maximum voluntary contraction
Time Frame: 72 hours
Maximum voluntary contraction will be assessed in kg on a custom made ergometer chair (COR 1)
72 hours
Delayed onset of muscle soreness
Time Frame: 72 hours
DOMS will be assessed using a visual analog scale (0-10 cm)
72 hours
Ratings of perceived exertion
Time Frame: 72 hours
RPE will be assessed using a BORG scale (6-20)
72 hours
Skin temperature
Time Frame: 60 minutes
Skin temperature of the neck, right scapula, right dorsal hand, right frontal thigh, right shin are assessed in °C using thermocouples (iButtons)
60 minutes
Core temperature
Time Frame: 60 minutes
Core temperature will be assessed in °C via the ear
60 minutes
Cardiovascular measurements
Time Frame: 60 min
Heart rate will be measured in beats per minute and bloop pressure will be measured in mm/Hg using an blood pressure monitor
60 min
Oxygenation of the right thigh muscle
Time Frame: 60 min
Oxygenation of the right thigh muscle will be assessed in % using a near infrared spectometer.
60 min

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ronaldus Clijsen, PhD, Fachhochschule Südschweiz

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

April 1, 2016

Primary Completion (Actual)

March 1, 2018

Study Completion (Actual)

June 1, 2018

Study Registration Dates

First Submitted

June 15, 2016

First Submitted That Met QC Criteria

July 25, 2016

First Posted (Estimate)

July 28, 2016

Study Record Updates

Last Update Posted (Actual)

August 8, 2019

Last Update Submitted That Met QC Criteria

August 7, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • PB_2016-01125

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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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