Muscle Damage

6

Review clinical trials related to Muscle Damage. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Photobiomodulation Effects on Fatigue and Muscle Damage Induced by NMES

Neuromuscular electrical stimulation (NMES) is widely used to improve muscle strength and mitigate atrophy. However, its clinical efficacy is often limited by early neuromuscular fatigue, muscle damage, and discomfort, which reduce patient tolerance and contraction time. Photobiomodulation (PBM) has emerged as a potential therapy to enhance muscle performance and accelerate recovery by minimizing fatigue and damage. Despite its potential, few studies have investigated the effects of PBM applied specifically before an NMES-evoked fatigue protocol. This randomized, double-blind, placebo-controlled trial aims to evaluate the acute effects of PBM on neuromuscular fatigue, muscle damage, and functional outcomes in healthy young subjects. Participants will receive either active PBM (cluster probe: 5 lasers 810nm/200mW; 4 LEDs 660nm/10mW; Total Energy: 249.6 J per limb) or sham treatment 5 minutes before a fatiguing NMES protocol (80 contractions at 20% MVIC, 80 Hz, 1ms pulse width) applied to the quadriceps muscle. Assessments will be performed at baseline, immediately post-intervention, and at 24h, 48h, and 72h post-intervention. Primary outcomes include maximum and evoked isometric strength, mechanical work, and electrical muscle activity. Secondary outcomes include muscle damage (ultrasound echo-intensity), delayed onset muscle soreness (DOMS), functional performance (unilateral vertical jump), and clinical discomfort. The study seeks to determine if PBM can effectively modulate NMES-induced fatigue and muscle damage, potentially optimizing its clinical application.

Participants needed: 36
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Federal University of Rio Grande do SulUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Healthy male and female volunteers. [+4]

Have sensory intolerable changes due to NMES [+4]

Status: Recruiting

Saskatoon Berry Juice for Muscle Recovery

This study will evaluated the effect of Saskatoon berry juice on recovery from muscle-damaging exercise.

Participants needed: 30
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: University of SaskatchewanUpdated: Apr 28, 2026Locations: 1
Eligibility criteria

Male or female [+1]

Conditions that might be affects by exercise as determined by the "Get Active Qu...

Status: Not yet recruiting

The Effects of Liquid IV's Multi-Ingredient Recovery Supplement on Muscle Recovery Following Exercise

The purpose of this study is to evaluate the efficacy of a multi-ingredient recovery supplement . The research will focus on strength recovery and performance maintenance assessing reductions in soreness and inflammation, as well as muscle repair and damage mitigation. By investigating these key recovery metrics, this study aims to investigate the efficacy of this supplement as a solution for active individuals seeking to optimize post-exercise recovery.

Participants needed: 30
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Applied Science & Performance InstituteUpdated: Apr 9, 2026Locations: 1
Eligibility criteria

Healthy males or females aged 18-55 years old. [+6]

Sedentary [+16]

Status: Not yet recruiting

Protein Distribution and Leucine Supplementation Effects on Body Composition and Performance in Tactical Athletes

This randomized controlled trial will examine the effects of within-day protein distribution and leucine supplementation on body composition, physical performance, and biomarkers of muscle damage in tactical athletes during an 8-week intensive training program. Sixty-nine healthy male participants (18-35 years) enrolled in a Ministry of Defense training course will be randomly assigned to one of three iso-caloric dietary groups providing 1.6 g/kg/day of protein: (1) evenly distributed protein across three meals (EVEN), (2) a 16-hour daily protein fasting pattern with protein concentrated at lunch and dinner (FAST), or (3) the same fasting pattern with 5 g leucine supplementation at breakfast (FAST-RESCUE). Primary outcomes include changes in lean body mass. Secondary outcomes include strength, anaerobic performance, and biochemical markers of muscle damage, including urinary titin N-terminal fragment (UTF). Assessments will be conducted at baseline, Week 5, and Week 8.

Participants needed: 69
Trial details
Age: 18-35Biological sex: MaleType: InterventionalSponsor: Tel Aviv UniversityUpdated: Mar 2, 2026
Eligibility criteria

Male participants aged 18-35 years [+4]

Musculoskeletal or neuromuscular injury or impairment limiting participation in... [+6]

Status: Recruiting

Comparing Two Eccentric Protocols on Muscle Damage

The purpose of this study will be to test whether a new way of weight training is more effective than typical weight training. The investigators expect that this new way will cause more exercise-induced muscle damage, which helps people build bigger muscles. Another purpose of this study will be to explore perceptions of how muscle soreness impacts participant activities of daily living.

Participants needed: 16
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: New York Institute of TechnologyUpdated: May 28, 2025Locations: 1
Eligibility criteria

Sixteen young adults (ages 18-35) will be enrolled in this study. [+1]

Since regular resistance training reduces the primary outcomes, muscle damage an... [+2]

Status: Recruiting

The Effect of Vicia Faba Hydrolysate Supplementation on Muscle Strength Recovery

To investigate the effect of Vicia faba protein concentrate, a protein derived from Fava bean extract, on delayed onset muscle soreness (DOMS). Participants receive either 2.4g/day of PeptiStrong® supplement capsules or placebo capsules for 14 days until a strenuous exercise session. For the last 3 days, 2/3 of them stay on the same treatment and 1/3 of them switch from placebo to PeptiStrong®.

Participants needed: 76
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: PepsiCo Global R&DUpdated: Feb 20, 2025Locations: 1
Eligibility criteria

Males and females 18 - 45 years of age. [+11]

Individuals that are glucose-6-phosphate-dehydrogenase deficient. The test produ... [+16]