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Not yet recruiting NCT06608836

Acute Effects of Cryotherapy on Muscle Properties

No phase Interventional Cryotherapy Effect

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An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: an ice massage, the cold spray.
Who it may be relevant to
Registry conditions: Cryotherapy Effect. Basic parameters: 18 years — 35 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Acute Effects of Cryotherapy on Muscle Mechanical Properties and Muscle Activation Changes

Overview

The main aim of this study is to investigate the acute effects of cryotherapy on muscle mechanical properties, muscle strength, and activation changes in healthy subjects.

Detailed description

What changes occur in muscle stiffness following cryotherapy application? How does cryotherapy affect muscle strength? How does cryotherapy impact muscle activation? Are there differences in muscle mechanical properties, muscle strength, and muscle activation between different cryotherapy methods (ice massage and cold spray)? How do the effects of cryotherapy on muscle mechanical properties, muscle strength, and muscle activation change over time?

Interventions

  • Other an ice massage
    an ice massage
  • Other the cold spray
    the cold spray

Primary outcome measures

  • myoton pro device [Time frame: 3 months]
  • muscle strength [Time frame: 3 months]
  • electromyography device [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • Being willing to participate in the study
  • Being between the ages of 18 and 35

Exclusion criteria

  • Having undergone orthopedic surgery involving the lower extremity

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06608836 · IstanbulOkanUni

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗