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Muscle Strength clinical trials

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NCT ID: NCT06460883 Not yet recruiting - Muscle Strength Clinical Trials

Effects of Eccentric Banded Leg Curls Versus Eccentric Cable Leg Curls Exercises in Cricket Players

Start date: June 2024
Phase: N/A
Study type: Interventional

Hamstring injuries are highly prevalent among cricket players, comprising 10% of all injuries in field-based team sports. Eccentric strength deficits and imbalances in muscle strength are linked to a higher risk of such injuries. Our randomized clinical trial aims to assess eccentric hamstring strength using eccentric banded leg curls and eccentric cable leg curl exercises, measured by the Nordbord device. This tool provides accurate measurements of eccentric hamstring strength, power, and endurance, crucial for injury prevention in athletes. Thirty-two male professional cricketers will participate, divided into two groups receiving different exercise plans. Each group will perform 15 reps in 3 sets with rest intervals, four times a week for four months. The Nordbord device will assess hamstring strength before and after the exercise plan. Statistical analysis will be done using SPSS V25, employing descriptive statistics for frequency distribution and inferential statistics such as t-tests to compare outcomes between treatment groups.

NCT ID: NCT06430879 Not yet recruiting - Muscle Weakness Clinical Trials

Performance Output With Haptics - Evaluating Athlete Response and Unrealized Potential

POWER-UP
Start date: July 10, 2024
Phase: N/A
Study type: Interventional

This minimal risk, randomized, double-blind, placebo controlled Institutional Review Board (IRB)-approved observational study with functional measurements, will evaluate athletic performance after use of a drug- free, non-invasive patch (VICTORY Patch; The Super Patch Company Inc.); using KangaTech, Catapult and Force Plates along with crossover control of trials within the same subject group not receiving an 'active' patch.

NCT ID: NCT06363409 Not yet recruiting - Muscle Strength Clinical Trials

The Acute and Accumulative Effects of Snack Foods on Exercise Recovery

Start date: June 1, 2024
Phase: N/A
Study type: Interventional

The purpose of the research is two-fold. One goal is to determine if post-exercise almond or cereal bar consumption can promote muscle gain as well as increasing muscular strength throughout an eight-week weight training program. The other goal is to assess the short-term effects of almonds or cereal bar on recovery that may explain the overall long-term adaptations.

NCT ID: NCT06321263 Not yet recruiting - Muscle Strength Clinical Trials

Comparison of the Effects of Peripheral Muscle Training and Inspiratory Muscle Training in Geriatric Individuals

Start date: March 25, 2024
Phase: N/A
Study type: Interventional

In geriatric individuals, there is a decrease in muscle strength, muscle mass and physical performance with ageing. These physiological changes occurring in geriatric individuals make maintaining the physical activity necessary for a healthy life difficult. Weakness of respiratory muscles in geriatric individuals can increase the prevalence of diseases and disability. It has been shown in the literature that peripheral muscle training and inspiratory muscle training increase exercise capacity similarly. The effectiveness of moderate-intensity peripheral muscle training and inspiratory muscle training in sarcopenic geriatric individuals was compared and found to have similar effects on muscle strength. Our study aims to compare the effects of inspiratory and peripheral muscle training in addition to aerobic exercise on muscle strength, physical performance, respiratory muscle strength, functional capacity, sarcopenia, and quality of life.

NCT ID: NCT06075901 Not yet recruiting - Muscle Strength Clinical Trials

Reliability and Performance Analysis of the Use of Tissue Flossing for Blood Flow Restriction.

Start date: May 1, 2024
Phase: N/A
Study type: Interventional

Blood flow restriction (RFS) is a widely studied technique that combines low-intensity exercise with vascular occlusion, resulting in muscular benefits. However, its application is challenging due to methodological variations and equipment costs. Tissue Flossing (TF) appears as an affordable alternative, but lacks solid scientific evidence.

NCT ID: NCT05510648 Not yet recruiting - Knee Osteoarthritis Clinical Trials

Evaluation of the Effect of High-intensity Laser Therapy in Knee Osteoarthritis

Start date: September 25, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effects of high intensity laser therapy (HILT) on range of motion, pain, quality of life, muscle strength and femoral cartilage thickness in patients with knee osteoarthritis.

NCT ID: NCT04888520 Not yet recruiting - Muscle Strength Clinical Trials

Strength and Muscle Activation of Runners Quadriceps After 8 Weeks of Intervention With Elastic Bandage

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

It is a controlled and randomized clinical trial with the objective of verifying the acute and chronic effects (8 weeks) of elastic banding in runners. Thus, we have as hypotheses of this research: The elastic bandage indirectly influences the muscular strength to the extent that it supposedly can alter the muscular activation verified through the surface electromyography in individuals submitted to the training as the running training. The elastic bandage has clinical significance, however, it does not present statistical significance on muscle strength and activation in individuals submitted to training as running training. To confirm these hypotheses, the muscle strength of the flexors and extensors of the right knee will be checked by means of the isokinetic dynamometer and the muscular activation of the extensors of the right knee (rectus femoris muscle) will be assessed by means of surface electromyography. The elastic bandage will be applied according to a specific protocol in "I" over the muscular belly of the right femoral rectus muscle (which will be submitted to evaluations). All participants will be evaluated without applying adhesive tape and will receive the first application of the tape without tension. Then, after 20 minutes of rest, they will be reassessed with the tape. Participants will be randomized into two groups and both will receive the adhesive tape (with or without tension according to randomization). Then the evaluations will be repeated (all will be reevaluated without the tape and with the tape (with or without tension according to the protocol).

NCT ID: NCT03853863 Not yet recruiting - Ultrasonography Clinical Trials

Minimalist Shoes Walking for Children

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

This is a single-blind randomized control study that will investigate the effects of a 12-week in-school walking training with minimalist shoes for local preschool children on intrinsic foot muscle size, muscle strength, and foot arch stiffness. The children in the control group will wear traditional footwear with arch support. It is hypothesized that walking with minimalist shoes may impose a positive impact to strengthen the IFM and promote foot arch stiffness for preschool children.

NCT ID: NCT03763513 Not yet recruiting - Pain Clinical Trials

Investigation of Acute Effect of ESWT and ESWT+KT on Pain and Grip Strength

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study was to investigate the acute effect of CT application in combination with ESWT and ESWT on pain and grip strength in athletes/patients with lateral epicondylitis.It is planned that at least 30 athletes aged 18-40 who are at the Ministry of Youth and Sports, Ministry of Health, Ministry of Health Affairs and who have been diagnosed with LE by specialist doctor. After taking the information about birth dates, height, weight and dominant sides of the athletes who are willing to participate in the study, pain intensities and hand grip strengths will be evaluated. Then the athletes will be randomly divided into 2 groups according to closed envelope method. First group ESWT application; 4 sessions will be held for 4 weeks. The second group included ESWT + CT; 4 sessions will be held for 4 weeks. Pain severity and hand grip strength will be evaluated again after treatment.

NCT ID: NCT03437239 Not yet recruiting - Shoulder Pain Clinical Trials

BFR After Bicep Tenodesis

Start date: February 2018
Phase: N/A
Study type: Interventional

A randomized controlled pilot study evaluating the effect of occlusion training on bone density and function of the upper extremity following a biceps tenodesis.