- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06565325
The Immediate Effect of Combined Terminal Knee Extension Exercise With Audible Cues
The Immediate Effect of Combined Terminal Knee Extension Exercise With Audible Cues on Vastus Medialis Muscle Motor Unit Behavior in Healthy Individuals
Typically, patients perform TKE by themselves after exercise prescription. The investigators thought that a lack of attention and preferred speed of patients might not provide the best outcome. Therefore, an increased effectiveness of TKE is interesting for physical therapy implication. Besides, adding sensory input which is audible cues or rhythm during exercise may enhance the efficacy of the exercise by increasing neuromuscular control and function.
Therefore, the study aimed to investigate the immediate effects of combined TKE with audible cues on motor unit behavior. The researchers expect that adding rhythm from the metronome will enhance neuromuscular control which may change motor unit behavior of VM muscle. The findings of the study may have helped explain the mechanism behind the acute effects of combined TKE with audible cues on VM function and their potential application in the field of physical therapy.
This study aims to investigate the immediate effect of combined TKE with audible cues on motor unit behavior in healthy participants and to investigate reliability of decomposition electromyography procedure during single leg squat.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Salaya
-
Nakhon Pathom, Salaya, Thailand, 73170
- Faculty of Physical Therapy, Mahidol University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged range between 18 and 30 years
- BMI of 18.5-25 kg/m2
- Male or female
- Lightly active or sedentary {Physical activity level (PAL= 1.4-1.69)}
Exclusion Criteria:
- History of serious injury or operation of lower back and lower extremities such as fracture
- Musculoskeletal problems of lower back and lower extremities in 6 months before the study
- Single-leg stance test < 43 seconds (26). and range of weight-bearing lunge test < 9.1 cm
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
Terminal Knee Extension Exercise with Audible Cues
|
Combined Terminal Knee Extension Exercise with Audible Cues
Other Names:
|
|
Active Comparator: Control group
Terminal Knee Extension Exercise without Audible Cues
|
Terminal Knee Extension Exercise
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Motor unit firing rate
Time Frame: At the end of Cycle 1 (each cycle is 1 day)
|
one parameter to explain the motor unit behavior of vastus medialis muscle
|
At the end of Cycle 1 (each cycle is 1 day)
|
|
Peak motor action potential
Time Frame: At the end of Cycle 1 (each cycle is 1 day)
|
one parameter to explain the motor unit behavior of vastus medialis muscle
|
At the end of Cycle 1 (each cycle is 1 day)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MU-CIRB 2024/021.0802
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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