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Muscle Strength clinical trials

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NCT ID: NCT06037798 Recruiting - Muscle Strength Clinical Trials

The Cranio-cervical Flexion Test Using the NOD Device

CCFT-NOD
Start date: November 8, 2023
Phase:
Study type: Observational

to measure strength of the deep anterior neck muscles with a new measurement protocol and by using the NOD device, a dynamometer, in subjects with and without bruxism, and compared to EMG on the superficial muscles of the anterior neck and the masseter muscle.

NCT ID: NCT05985967 Recruiting - Muscle Strength Clinical Trials

Therapeutic Modalities on Exercise Performance and Post-exercise Recovery of CrossFit® Athletes

Start date: August 9, 2023
Phase: N/A
Study type: Interventional

Crossfit® is a training modality that consists in functional movements, constantly varied and executed at high intensity. Both training sessions and competitions involve physically demanding activities, which in addition to being performed at very high intensity also involves the aerobic metabolism pathway. These characteristics led to very high metabolic and muscular stress, as well as decrease in physical performance immediately after competitions and training sessions. The cumulative effects of the metabolic and muscular stress can be a precursor of injuries. Studies using different therapeutic modalities aiming to improve post-exercise recovery are needed in order to tackle this issue. However, to the date there are no studies investigating the effects of different therapeutic modalities in an exercise modality such as Crossfit®. Therefore, the aim of this project is to assess the effects of different therapeutic modalities on performance and muscle recovery of Crossfit® athletes.

NCT ID: NCT05945641 Recruiting - Muscle Strength Clinical Trials

Effect of Low-load Resistance Training vs. High-intensity Interval Training on Local Muscle Endurance

LLSIT
Start date: September 27, 2023
Phase: N/A
Study type: Interventional

Local muscle endurance (LME) is the ability of a muscle(s) to resist fatigue and is needed for daily activities of life such as climbing stairs, lifting/moving objects, and in sport contexts like rock climbing, mixed martial arts, cross-fit, kayaking and canoeing. Therefore, the investigators want learn how to improve LME and understand what in human bodies changes during exercise training to cause these changes. The investigators know that lifting weights improves muscle strength which is believed to improve LME. Specifically lifting less heavy weights (LLRET) for more repetitions leads to greater gains in LME opposed to heavier weights for fewer repetitions. Therefore, lifting less heavy weights likely causes greater changes in our muscles than lifting heavier weights that cause improvements in LME. Aerobic exercise preformed at high intensities in an interval format (HIIT) may also help improve LME by increasing our muscle's ability to produce energy during exercise. Therefore, the investigators want to see which of LLRET or HIIT leads to greater improvements in LME.

NCT ID: NCT05932875 Recruiting - Body Composition Clinical Trials

Peanut Consumption to Augment Adaptations to Concurrent Resistance and Aerobic Exercise Training

Start date: May 30, 2023
Phase: N/A
Study type: Interventional

The primary objective of this proposal is to determine the effects of post-exercise peanut consumption on long-term aerobic and resistance exercise training adaptations in middle-aged men and women. We will determine the impact of peanuts on exercise training-induced improvements in muscle strength, gains in muscle mass, and improvements in cardiorespiratory fitness and metabolic capacity.

NCT ID: NCT05710614 Recruiting - Diet Habit Clinical Trials

Distinct Sources of Supplementary Protein in the Resistance Exercise Training-induced Adaptations

Start date: August 1, 2023
Phase: N/A
Study type: Interventional

This is a randomized controlled trial aimed to investigate the effects of different supplementary protein sources on muscle adaptations to resistance exercise. Young, healthy, recreationally active participants consuming an omnivorous diet with protein intake within recommended dietary allowance (RDA) (i.e.; 0.8-1.0 g.kg-1. d-1) will be recruited to undergo a 12-wk supervised resistance training program in combination with the intake of three 15-g daily doses (45g. d-1 total) of either a mixed plant- (i.e.; soy and pea protein) or animal-based (i.e.; whey protein) protein in drink form as a supplementary source of protein to their main meals of the day (i.e.; breakfast, lunch, and dinner). Before (PRE) and after (POST) the 12-wk intervention, participants will be assessed for body composition by dual-energy X-ray absorptiometry (DXA), muscle cross-sectional area (ultrasound) and fiber cross-sectional area (muscle biopsy), and maximal isotonic strength (1RM). Training consists of a resistance training (RT) program individually supervised by a researcher blinded to treatment in a laboratorial setting. Assessments will also be conducted in a blinded fashion.

NCT ID: NCT04849624 Recruiting - Covid19 Clinical Trials

Body Composition Study in Critically Ill Patients-Extended to COVID-19

COVID-MUSCLE
Start date: March 5, 2021
Phase:
Study type: Observational

Muscle loss (ultrasound quadricep muscle) and muscle strength (handgrip and knee extension strength) will be compared between COVID-19 and non COVID-19 critically ill patients.

NCT ID: NCT04741373 Recruiting - Body Composition Clinical Trials

Study on Pulmonary Rehabilitation for Stable Chronic Obstructive Pulmonary Disease(COPD) Patients

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

To compare the difference of effectiveness for stable COPD patients with poor nutritional status among three groups named health education, upper and lower limb exercises, and oral nutritional supplements. Then formulate the best pulmonary rehabilitation guidance strategy according to the result of this trial.

NCT ID: NCT04503486 Recruiting - Quality of Life Clinical Trials

Relationship Between Muscle Strength and Quality of Life in ICU Survivors

Start date: August 1, 2020
Phase:
Study type: Observational

The aim is to study the impact of muscle strength measured in ICU and after ICU discharge on health-related quality of life measured after hospital discharge.

NCT ID: NCT04312529 Recruiting - Muscle Strength Clinical Trials

Analysis of Shoulder Muscle Activity During Isokinetic Evaluation of Rotators

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

The objective of this study is to assess the impact of different positions of the glenohumeral joint on the maximum muscle contraction of different shoulder muscles. The muscles do not contract with the same intensity depending on the position of the arm in relation to the trunk. With the determination of this optimal position to activate the shoulder muscles as much as possible, we will be able to strengthen the patients during their revalidation.

NCT ID: NCT04277364 Recruiting - Muscle Strength Clinical Trials

Effects of Phosphatidic Acid on Strength and Hypertrophy

Start date: August 17, 2020
Phase: N/A
Study type: Interventional

There are indications that phosphatidic acid (PA) supplementation is capable of enhancing gains in strength and muscle mass in response to strength training, although the literature is still incipient and controversial. Given the possible benefits in terms of maintenance and increased skeletal muscle mass, which still need confirmation, this study aims to examine the effectiveness of PA supplementation in two different doses in increasing skeletal muscle mass and strength in adult men undergoing to 8 weeks of strength training. For this, about 45 men will be randomly allocated to one of three treatments at a ratio of 1:1:1: PA 750mg per day, PA 375mg per day, or placebo (cornstarch, 750mg per day). All participants will undergo a 8-week strength training program, 3 times a week, totaling 24 sessions, which will begin with the start of supplementation. Individuals will be assessed for maximum dynamic strength of upper and lower limbs, resistance to dynamic strength of upper and lower limbs, body composition, muscle cross-sectional area and food consumption. Samples of venous blood will also be collected to determine the concentration of creatine kinase (CK), lactate dehydrogenase (LDH), testosterone, insulin-like growth factor type 1 (IGF-1), growth hormone (GH) and cortisol. These evaluations will be carried out before (PRE) and after (POST) the period of supplementation and training. Additional blood samples will be taken 48 hours after the first and last training sessions, for specific determination of blood muscle damage markers: CK and LDH.