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Completed

NCT Number: NCT05757518

Post-exercise Recovery of DOMS in Recreational Athletes

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.

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Key information

Age range

20 year–26 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Physical Exercise Laboratory

Gdansk, 80-336, Poland

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Cryosauna

Other

The intervention was Cryosauna - cryostimulation at -110°C for 1.5 minutes, for four consecutive days.

Primary outcomes

  1. 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.

  2. Measurement of blood markers.

    Time frame: Change from baseline leukocytes concentration at 96 hours after fatigue-induced exercise.

    Leukocytes [10^9 /L] concentration.

  3. Measurement of blood markers.

    Time frame: Change from baseline creatine kinase concentration at 96 hours after fatigue-induced exercise.

    Creatine kinase [ng/mL] concentration.

  4. Measurement of blood markers.

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

    Myoglobin [ng/mL] concentration.

Sponsors and collaborators

Lead sponsor

Wroclaw University of Health and Sport Sciences

Other

Collaborators

  • Gdansk University of Physical Education and Sport

Registry information

Official study title

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

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Mar 7, 2023
Registry last updated
Mar 7, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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