- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04977999
Effects of Combining Eccentric and Aquatic Based Exercise on Muscle Function
April 19, 2024 updated by: Brennan Thompson
Comparative Effects of Eccentric-driven Exercise on Measures of Muscle Function When Combined With Aquatic Plyometric Exercise
The study will compare the effects of eccentric resistance training versus eccentric training combined with aquatic plyometric training on muscle function outcomes.
Study Overview
Detailed 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.
Study Type
Interventional
Enrollment (Actual)
35
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Utah
-
Logan, Utah, United States, 84322
- Utah State University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 30 years (Adult)
Accepts Healthy Volunteers
Yes
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Eccentric training
Eccentron (BTE Technologies, Inc.) training
|
Both arms/conditions use varying forms of exercise as the intervention.
|
Experimental: Aquatic training
Hydroworks aquatic training
|
Both arms/conditions use varying forms of exercise as the intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Countermovement jump
Time Frame: 7 weeks
|
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
|
Depth jump
Time Frame: 7 weeks
|
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
|
Maximal isometric strength
Time Frame: 7 weeks
|
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
|
Maximal eccentric strength
Time Frame: 7 weeks
|
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
|
40-m sprint
Time Frame: 7 weeks
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle soreness
Time Frame: 7 weeks
|
local muscle soreness will be assessed throughout the duration of the intervention period using a Wagner force algometer.
|
7 weeks
|
Muscle soreness (visual analog scale)
Time Frame: 7 weeks
|
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
|
Inertial measurement unit
Time Frame: 7 weeks
|
3-axis microelectromechanical systems (MEMS) accelerometers (Blue Trident, Vicon Motion Systems) to assess center of mass during countermovement jumps
|
7 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Brennan J Thompson, PhD, Utah State Univeristy
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 21, 2021
Primary Completion (Actual)
May 1, 2022
Study Completion (Actual)
May 16, 2022
Study Registration Dates
First Submitted
July 21, 2021
First Submitted That Met QC Criteria
July 26, 2021
First Posted (Actual)
July 27, 2021
Study Record Updates
Last Update Posted (Actual)
April 23, 2024
Last Update Submitted That Met QC Criteria
April 19, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 11903 (DAIDS ES)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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