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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04977999
Other study ID # 11903
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date September 21, 2021
Est. completion date May 16, 2022

Study information

Verified date April 2024
Source Utah State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study will compare the effects of eccentric resistance training versus eccentric training combined with aquatic plyometric training on muscle function outcomes.


Description:

This study will use a parallel, randomized group design. Two groups will be randomly formed with one group comprising an eccentric only resistance training condition (experimental control) and the other comprising an eccentric combined with aquatic-based plyometrics condition (experimental). All subjects, regardless of group, will train on a multiple-joint eccentric machine one time per week for 7 weeks. The combined group will also perform an aquatic-based exercise session one time (on a separate day from the eccentric training) per week. Muscle function will be assessed via a battery of tests including jumps, sprints, and isometric and eccentric maximal strength.


Recruitment information / eligibility

Status Terminated
Enrollment 35
Est. completion date May 16, 2022
Est. primary completion date May 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - 18 - 30 years Exclusion Criteria: - Currently doing resistance exercise > 3 times per month or aerobic exercise at or more than 30 min, 5 days per week. - Any lower limb injuries or surgery within a year of the study - If any of the subject's are too tall for the Eccentron machine (>76 inches tall) - If any of the subject's eccentric strength is measured to be greater than 725 pounds during the first test of eccentric strength.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise
Both arms/conditions use varying forms of exercise as the intervention.

Locations

Country Name City State
United States Utah State University Logan Utah

Sponsors (1)

Lead Sponsor Collaborator
Brennan Thompson

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Countermovement jump Participants will perform three maximal counter movement vertical jumps on a force platform. Participants will be instructed to stand on the platform with their feet shoulder width apart with their hands on their hips. Participants will be instructed to quickly lower themselves to a comfortable depth then immediately jump as high as possible while landing with their legs relatively straight (Crane et al., 2020). A successful countermovement jump attempt will be counted if the participant lands on the platform with both feet and does not take a step before jumping (Palmer et al., 2014). A 1-minute rest period will be provided between each jump attempt. Participants will be asked to perform three practice jumps with their hands placed on hips. Following the completion of practice jumps, participants will perform 3 trials of countermovement jumping on land and 3 trials while immersed in water at waist-depth. 7 weeks
Primary Depth jump Participants will perform three maximal-effort depth jumps from a height of 0.4 meters onto a force plate. Participants will be instructed to step straight off of the box without lowering themselves prior to falling, then to land and quickly jump as high as they can with minimal ground contact time. A successful jump attempt requires landing on the force plate with both feet both from the drop as well as from the rebound jump. A 1-minute rest period will be provided between each jump attempt. 7 weeks
Primary Maximal isometric strength Participants will be tested on a custom-made isometric mid-thigh pull (IMTP) device. This device consists of a force plate set onto an aluminum plate to which a bar is attached via chains, which are adjustable for height. The subject will be fitted with an over-the-shoulder vest which will be secured to straps fixed to the force plate. The straps will be adjusted so that the participant's knee angle is set within a range of 125-145°, and the hip angle in a range of 140-150°, as has been suggested to be optimal (Comfort et al., 2019). Participants will be instructed to stand on the plate with feet shoulder width apart, and then to move to a point where the slack is all out of the straps. To initiate the pull, participants will be instructed to drive their feet through the floor as hard and as fast as they can, while keeping their feet and upper body in position, starting on the signal, and not performing a countermovement prior to the pull. 7 weeks
Primary Maximal eccentric strength Eccentric muscle strength will be assessed via Eccentron (BTE Technologies, Inc., USA), a seated isokinetic dynamometer. . The pedals will move toward the participant in an alternating motion, so that each leg will work isolaterally in a repetitive manner. There will be a total of 12 maximal effort repetitions, six for each leg. For testing purposes, the speed of this motion will be set at 23 cycles per minute, which is defined as a moderate speed (Gordon et al., 2019). 7 weeks
Primary 40-m sprint Participants will perform three maximal-effort 40-m sprints on a hard track surface in accordance with procedures outlined by (Gordon et al., 2019). Sprint time will be measured by timing gates (Dashr Motion Performance Systems, Dashr LLC, Lincoln, Nebr., USA) positioned at the start and end points of the run distance. Participants will be instructed to start in a 3-point stance with their feet staggered and one hand on the ground. For the three point stance, participants will be instructed to place the front of their lead foot on a line 30 cm behind the start line, and to place the opposite hand of the lead foot on the starting line (Rimmer & Sleivert, 2000). The sprint will be started with the use of a verbal command and participants will be instructed to run through a line 10 meters past the second timing gate to ensure they give full effort throughout the entire measured distance. Three trials of sprints will be performed, with a rest period of two minutes between each trial. 7 weeks
Secondary Muscle soreness local muscle soreness will be assessed throughout the duration of the intervention period using a Wagner force algometer. 7 weeks
Secondary Muscle soreness (visual analog scale) During the course of the training period, soreness levels will be assessed using a visual analog scale (VAS), in accordance with our previous procedures (Crane et al., 2020). The VAS will be administered at baseline (prior to the first training session) and for five consecutive days following the first training session of the first experimental week and then on three nonconsecutive, non-training days per week for the remaining six weeks (Crane et al., 2020). 7 weeks
Secondary Inertial measurement unit 3-axis microelectromechanical systems (MEMS) accelerometers (Blue Trident, Vicon Motion Systems) to assess center of mass during countermovement jumps 7 weeks
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