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Resistance Training clinical trials

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NCT ID: NCT04241991 Completed - Aged Clinical Trials

Photobiomodulation (PBM) Therapy on Muscle Performance in Elderly Women

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

The present project aims to investigate the acute and chronic effects of laser photobiomodulation (PBM) at 808 nm on muscle performance in physically active elderly women. The hypothesis of this study is that laser PBM would improve muscle strength (i.e., MVIC and 1RM) and endurance (i.e., repetitions-to-failure, blood lactate levels), functional capacity (i.e., short physical performance battery score), and rating of perceived exertion when compared with placebo laser.

NCT ID: NCT04213586 Completed - Exercise Clinical Trials

Effects of Whey Protein and Collagen Supplementation

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

The present project aims to investigate the effects of high-quality protein (whey protein) vs. low-quality protein (collagen) on muscle mass and function (e.g., strength and power) during a 10-wk resistance training program in young adults. It will be tested the hypothesis that leucine-matched collagen should promote similar gains on muscle function and mass compared to whey protein supplementation.

NCT ID: NCT04207567 Completed - Resistance Training Clinical Trials

Minute Calisthenics: A Daily, Habit-Based, Bodyweight Resistance-Training Program

Start date: November 11, 2019
Phase: N/A
Study type: Interventional

As the primary objective, this study will evaluate the effectiveness, in terms of changes in physical strength, of a resistance training (RT) program consisting of brief bodyweight exercises (<5 min/day) performed unsupervised every weekday for 12 weeks. Blood pressure, lipid profile, hemoglobin A1ca, habit strength and satisfaction with the program will also be assessed. Office workers and osteopathic medical students will serve as participants.They will be randomized (1:1) to the intervention group or to a waitlist control group that will refrain from RT for the initial 12 weeks. After the 12-week follow-up assessment, the intervention group will continue the program and the waitlist control group will start the program for 12 weeks, followed by a 24-week follow-up assessment.

NCT ID: NCT04136821 Completed - Oxidative Stress Clinical Trials

The Long-term Effects of Oceanix™ on Resistance Training Adaptations

Start date: September 30, 2019
Phase: N/A
Study type: Interventional

This study will examine the effects of Oceanix™, an antioxidant supplement, on muscle performance, immune and endocrine function, recovery and safety in participants undergoing resistance training. Measures of muscle performance will include isometric testing in the bench-press and mid-thigh pull and ground reaction forces in the counter movement- and squat-jump. Markers of immune function will include salivary immunoglobulin A (IgA) as well as serum total antioxidant capacity (TAC) and superoxide dismutase (SOD) while endocrine function will be measured by salivary cortisol and testosterone. Recovery will be measure by plasma creatine kinase (CK) and perceptual measures will be assessed using a validated perceived recovery status (PRS) scale. Safety metrics will be indicated by a comprehensive metabolic panel (CMP), complete blood count (CBC), and urinalysis (UA). Additionally, the modified Borg Rating of Perceived Exertion (RPE) will be administered following each training session to grade physical exertion and monitor progression of the training protocol.

NCT ID: NCT04069351 Completed - Weight Gain Clinical Trials

Body Composition Changes During Overfeeding Plus Resistance Training

Start date: September 18, 2019
Phase: N/A
Study type: Interventional

This study will examine the relationship between the rate and composition of mass gain during overfeeding plus resistance training, investigate the validity of multiple assessment methods for quantifying body composition changes during this period, and evaluate the effects of subject presentation on the interpretation of body composition changes.

NCT ID: NCT04044638 Completed - Blood Pressure Clinical Trials

Eight Week Strength Training Reduces Blood Pressure of Middle Age Women

Start date: March 5, 2018
Phase: N/A
Study type: Interventional

Introduction: Strength training (ST) is an important non-pharmacological means to reduce blood pressure (BP). Objective: To verify the pressure response of women after 8 weeks of ST. Method: Fourteen women were divided into young group (YG) and middle age (MAG) and submitted to ST for 8 weeks, lasting 60 minutes in 11 alternating exercises per segment with intensity of 12 to 13 on the subjective perception scale of effort. BP was verified at weeks 1, 4 and 8.

NCT ID: NCT04022707 Completed - Resistance Training Clinical Trials

High Speed Circuit Training and Cognition

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

The purpose of this research study is to see if a weight training program can make a positive change in participant fitness as measured by the ability to use oxygen and help the participant remember things.

NCT ID: NCT03957746 Completed - Hypertension Clinical Trials

Set Volume of Optimal Resistance Exercise to Generate Hypotension

Start date: May 13, 2020
Phase: N/A
Study type: Interventional

This study evaluates the volume of optimal resistance exercise to generate postexercise hypotension after performing a single exercise in hypertensive elderly subjects. 20 subjects will perform 1 control session and 3 resistance training sessions with different volume: 3, 6 and 9 sets

NCT ID: NCT03889548 Completed - Resistance Training Clinical Trials

Influence of Resistance Training Experience and Mental Imagery on Corticospinal Excitability and Inhibition

Start date: February 7, 2019
Phase: N/A
Study type: Interventional

This study will utilize transcranial magnetic stimulation (TMS) to examine the effects of mental imagery in resistance-trained versus untrained men and women. In randomized order, each participant will perform a mental imagery task or a control condition as TMS is used to study corticospinal excitability.

NCT ID: NCT03862560 Completed - Resistance Training Clinical Trials

Evaluation of Physical Performance and Functional Asymmetries in Female Football

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

Worldwide, soccer has grown increasingly popular among female players. According to the Women´s Football Survey of the Fédération Internationale de Football Association (FIFA), there were more than 30 million registered women soccer players in 2014. Elite female soccer players cover approximately a total distance of 10 km with 1.7 km completed at high-speed (>18 km/h-1), between 1350 and 1650 changes of activity like passing, dribbling, tackling and trapping and 5.1 and 31.2 repeated sprinting and high intensity bouts, respectively. Thus, it seems that those strategies addressed to improve such high-intensity activities should be considered a priority for female soccer players. Different training methods to improve soccer specific variables have been developed such as, high-intensity interval training, resisted sprint training, strength training or plyometric training. Whilst individual training interventions have been shown to produce enhancements in measures of athletic performance for soccer players, there is a paucity of studies looking at the effectiveness of strength and power training specifically on performance measures in female soccer populations. Unilateral strength asymmetry can be a risk factor of musculoskeletal injuries. In recent years, inter-limb asymmetries have been included in battery tests performed by different soccer clubs due to their relation with lower-limb injuries. Few studies have analysed the change of an intervention on inter-limb asymmetry in female soccer players, hence, more studies for this population are warranted. The main aim of this research project is therefore, to evaluate the effect of a physical intervention on the performance and inter-limb asymmetries of female soccer players.