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Clinical Trials/NCT05757518
NCT05757518
Completed
Not Applicable

Cryosauna for Post-exercise Recovery of Delayed Onset Muscle Soreness (DOMS) in Recreational Athletes: a Randomized Control Trial

Wroclaw University of Health and Sport Sciences1 site in 1 country36 target enrollmentStarted: January 16, 2023Last updated:
ConditionsInjury;Sports

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Wroclaw University of Health and Sport Sciences
Enrollment
36
Locations
1
Primary Endpoint
Measurement of blood markers.

Overview

Brief Summary

The main goal of this study was to investigate the effectiveness of cryo-sauna in preventing the development of DOMS in the lower extremity. The second goal is to analyze the rate of regenerative changes in the right muscles after acute fatigue-induced exercises.

Detailed Description

The main goal of this study was to investigate the effectiveness of cryo-sauna in preventing the development of DOMS in the lower extremity. The second goal is to analyze the rate of regenerative changes in the right muscles after acute fatigue-induced exercises.

This study design was a randomized, controlled single-blind trial with repeated measures. Moreover, the design was prepared according to the Consolidated Standards of Reporting Trials (CONSORT) for pragmatic trials. Participants were assigned into two groups: (1) experimental group (CRYO, n =16) - cryostimulation using a cryo sauna; and (2) control group (CONT, n = 15) - without any intervention. This study was conducted in the Physical Exercise Laboratory. Both groups, CRYO and CON performed a fatigue-induced protocol consisting of counter-movement jumps (CMJ) (10 set for 10 repetitions). After the fatigue exercises, only CRYO underwent cryo sauna intervention including entry immediately after, 24, 48, and 72 hours post-exercise. The order of measurements at baseline included: blood sample testing (creatine kinase, myoglobin, leukocytes) and muscle stiffness of the lower extremity. All measurements we collected at baseline, immediately post, 24, 48, 72, and 96 hours post-exercise.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Screening
Masking
Double (Investigator, Outcomes Assessor)

Masking Description

Participants will be allocated to intervention (cryostimulation using cryosauna) or a control group (without any intervention) using a randomized list of allocated numbers generated by a computer program. The investigator and Outcomes Assessor will be blinded to the allocation process.

Eligibility Criteria

Ages
20 Years to 26 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • no previous experience with cryostimulation using a cryo-sauna,
  • recreational lifestyle.

Exclusion Criteria

  • Current or prior pain or injury in the lower extremity.
  • Previous history of surgery in the lower extremity.
  • Cardiovascular disabilities.

Outcomes

Primary Outcomes

Measurement of blood markers.

Time Frame: Change from baseline myoglobin concentration at 96 hours after fatigue-induced exercise.

Myoglobin \[ng/mL\] concentration.

Measurement of muscle stiffness in the lower extremity.

Time Frame: Change from baseline muscle stiffness at 96 hours after fatigue-induced exercise.

Stiffness \[N/m\] was measured on: the anterior thigh, posterior thigh, shin, and calf muscles in 23 reference points.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Wroclaw University of Health and Sport Sciences
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sebastian Klich

Study Director

Wroclaw University of Health and Sport Sciences

Study Sites (1)

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