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Feasibility of Assessing Muscle Displacement and Muscle Excursion on Muscle Fatigue, With and Without Preventive Strategies

Not Applicable
Active, not recruiting
Conditions
Muscle Fatigue
Registration Number
NCT07102602
Lead Sponsor
National Taiwan University Hospital
Brief Summary

Study Subjects: This study will recruit healthy males aged 18 to 35 who regularly exercise for at least 2.5 hours per week.

Expected Number of Participants: 20.

Methods and Procedures: This trial will be randomized into two groups, Groups A and B, who will undergo two isokinetic concentric exercise sessions (fatiguing exercise) separated by 15 days. Group A will first receive a fatigue prevention strategy (high-energy laser) followed by a placebo-controlled no-fatigue strategy 15 days later. Group B will first receive a placebo-controlled no-fatigue strategy followed by a fatigue prevention strategy (high-energy laser) 15 days later. The fatigue prevention strategy involves irradiating the quadriceps femoris with a 900-joule high-intensity laser therapy (3-watt output power for 5 minutes) before the isokinetic concentric exercise. The no-fatigue strategy (sham-controlled) involves irradiating the quadriceps femoris with a 0-joule high-energy laser (0-watt output power for 5 minutes) before the isokinetic concentric exercise. Muscle displacement, muscle excursion, as well as muscle electrophysiological changes, force output, and microcirculation parameters were measured before and after exercise to verify the feasibility of muscle displacement and migration for muscle fatigue assessment, and to further establish their impact and application value in muscle fatigue prevention strategies (high-intensity laser therapy).

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
Male
Target Recruitment
20
Inclusion Criteria
  • healthy male aged between 18 and 35 years who engage in regular physical activity for at least 2.5 hours per week
Exclusion Criteria
  • history of musculoskeletal injuries or lower limb muscle strains involving the dominant lower limb within the past six months
  • history of surgical interventions on the dominant lower limb

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
Muscle displacementpre-fatigue (baseline), immediately post-fatigue, 5, 10, 20 minutes post-fatigue
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

National Taiwan University College of Medicine

🇨🇳

Taipei, Taipei city, Taiwan

National Taiwan University College of Medicine
🇨🇳Taipei, Taipei city, Taiwan

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