- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07507695
Acute Effects of Patellar Tendon Ultrasound on Countermovement Jump Performance
Acute Effects of Therapeutic Ultrasound Applied to the Patellar Tendon on Countermovement Jump Performance: A Randomized Controlled Trial
This randomized, double-blind, controlled trial aims to investigate the acute effects of therapeutic ultrasound applied to the patellar tendon on vertical jump performance in healthy university students. Therapeutic ultrasound is widely used in physiotherapy to influence soft tissue properties through thermal and mechanical effects; however, its immediate impact on explosive lower-extremity performance and neuromuscular function remains unclear.
Participants will be randomly assigned to either a therapeutic ultrasound group or a sham ultrasound (placebo) group. In the intervention group, therapeutic ultrasound will be applied to the patellar tendon using a frequency of 1 MHz and an intensity of 1.5 W/cm² in continuous mode for 5 minutes. In the control group, a sham ultrasound procedure will be performed using the same device and duration without delivering therapeutic energy. Both the participants and the outcome assessor will be blinded to group allocation.
Vertical jump performance will be evaluated using the countermovement jump (CMJ) test recorded with the My Jump 2 smartphone application. In addition, quadriceps muscle strength will be measured using a hand-held dynamometer, and knee joint position sense will be assessed using a joint position reproduction test. All measurements will be conducted before and immediately after the intervention.
This study will provide evidence regarding whether therapeutic ultrasound applied to the patellar tendon can acutely influence explosive performance, muscle strength, and proprioception in healthy individuals.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This randomized, double-blind, controlled trial aims to investigate the acute effects of therapeutic ultrasound applied to the patellar tendon on vertical jump performance, quadriceps muscle strength, and knee joint proprioception in healthy university students. Therapeutic ultrasound is a commonly used physiotherapy intervention that can induce thermal and mechanical effects on soft tissues; however, its immediate impact on explosive lower-extremity performance and neuromuscular function has not been fully established.
A total of healthy participants aged 18-35 years will be recruited and screened according to predefined inclusion and exclusion criteria. Eligible participants will be randomly assigned to either a therapeutic ultrasound group or a sham (placebo) ultrasound group. The intervention group will receive therapeutic ultrasound applied to the patellar tendon at a frequency of 1 MHz, intensity of 1.5 W/cm², in continuous mode for 5 minutes. The sham group will undergo the same procedure without delivery of therapeutic energy. Both participants and the outcome assessor will be blinded to group allocation, ensuring a double-blind design.
Outcome measures will be recorded immediately before and within one minute after the intervention. Vertical jump performance will be assessed using the countermovement jump (CMJ) recorded with the My Jump 2 smartphone application. Quadriceps muscle strength will be measured using a hand-held dynamometer, and knee joint position sense will be evaluated using a joint position reproduction test. Participants will perform three trials for each measure, with 60-second rest intervals between trials, and the best value will be used for analysis. Familiarization trials will be conducted prior to testing to minimize learning effects.
This study will provide evidence on whether therapeutic ultrasound applied to the patellar tendon can acutely influence explosive performance, quadriceps strength, and proprioception in healthy individuals, which may inform clinical and sports performance applications.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Cengiz TAŞKAYA
- Phone Number: 05364811882
- Email: c.taskaya@alparslan.edu.tr
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy university students aged 18-35 years
- No history of lower extremity injury or surgery in the past 12 months
- No current musculoskeletal or neurological disorders affecting the lower limbs
Exclusion Criteria:
- History of patellar tendon injury or knee pain
- Contraindications to therapeutic ultrasound (e.g., skin lesions, open wounds at the knee, or implanted electronic devices)
- Any cardiovascular, neurological, or musculoskeletal condition that may affect jump performance
- Use of medications that could affect neuromuscular function (e.g., muscle relaxants)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Ultrasound Group
The use of therapeutic ultrasound in healthy individuals
|
The use of therapeutic ultrasound on the patellar tendon in healthy individuals.
|
|
Sham Comparator: sham Group
Use of sham ultrasound in healthy individuals
|
The use of therapeutic ultrasound on the patellar tendon in healthy individuals.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Countermovement Jump Height
Time Frame: Immediately before and immediately after the intervention (within 1 minute following the ultrasound or sham ultrasound application)
|
Vertical jump performance will be assessed using the countermovement jump (CMJ) test recorded with the My Jump 2 smartphone application.
Participants will perform three maximal jumps with their hands placed on their hips to eliminate arm swing, and the highest jump height (cm) will be used for analysis.
|
Immediately before and immediately after the intervention (within 1 minute following the ultrasound or sham ultrasound application)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee Joint Position Sense
Time Frame: Immediately before and immediately after the intervention
|
Knee joint position sense will be assessed using a joint position reproduction test to evaluate proprioception.
Participants will actively reproduce a predetermined knee flexion angle without visual feedback, and the absolute angular error (degrees) between the target and reproduced position will be recorded.
|
Immediately before and immediately after the intervention
|
|
Quadriceps Muscle Strength
Time Frame: Immediately before and immediately after the intervention
|
Quadriceps muscle strength will be measured using a hand-held dynamometer.
Participants will perform maximal voluntary isometric knee extension while seated with the knee flexed at 90 degrees.
The highest value obtained from three trials will be recorded in kilograms (kg) for analysis.
|
Immediately before and immediately after the intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Burhan TAŞKAYA, Muş Alparslan University
- Principal Investigator: Cengiz TAŞKAYA, Muş Alparslan University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- Therapeutic Ultrasound
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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