- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07532980
Quadriceps and Hamstring Activation Timing
April 9, 2026 updated by: KTO Karatay University
Quadriceps and Hamstring Activation Timing During Functional Tasks Following ACL Reconstruction
The anterior cruciate ligament (ACL) plays a crucial role in maintaining knee stability and enabling dynamic movement.
ACL injuries are common, especially among athletes, and reconstruction surgery is frequently performed to restore knee function.
Despite rehabilitation, neuromuscular deficits-particularly in muscle activation timing-may persist.
This study will aim to evaluate the activation timing of quadriceps and hamstring muscles during a functional task in individuals who have undergone ACL reconstruction.
Study Overview
Status
Enrolling by invitation
Intervention / Treatment
Detailed Description
This study will be conducted as a cross-sectional, quantitative investigation involving male participants who have undergone ACL reconstruction using semitendinosus and gracilis tendon grafts.
Electromyographic (EMG) signals will be collected using the Noraxon Ultium EMG system and analyzed with Noraxon MyoResearch XP software.
Muscle activation onset timing will be assessed for the vastus medialis oblique (VMO), vastus lateralis (VL), semimembranosus (SM), semitendinosus (ST), and biceps femoris (BF).
Participants will perform a standardized single-leg squat task, during which EMG-based activation timing will be recorded.
The findings are expected to provide insight into neuromuscular control strategies and inform rehabilitation approaches following ACL reconstruction.
Study Type
Observational
Enrollment (Estimated)
25
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
-
-
Karatay
-
Konya, Karatay, Turkey (Türkiye), 42030
- KTO Karatay 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
- Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
The study population will consist of male individuals aged 18-45 years who have undergone anterior cruciate ligament (ACL) reconstruction using semitendinosus and gracilis tendon grafts.
Description
Inclusion Criteria:
- participants must be males between 18 and 45 years old
- must have undergone ACL repair surgery and be within 6 months to 2 years post-surgery
- should have completed a standard rehabilitation program post-surgery
- must provide written informed consent to participate in the study
- should be in generally good health, without any other significant medical conditions that could affect the study outcomes;
- must have returned to a moderate level of physical activity post-surgery
Exclusion Criteria:
- participants with any neurological disorders affecting lower limb function or any other musculoskeletal disorders or injuries that could affect the lower limb, apart from the ACL injury
- those with cardiovascular conditions that contraindicate participation in physical activity
- those with contraindications to kinesiological electromyography, such as skin conditions or allergies to electrodes
- those who are unable or unwilling to comply with study procedures and follow-ups
- those who have had multiple ACL surgeries on the same knee
- participants involved in ongoing litigation related to their ACL injury
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Electromyography
Time Frame: Single session (approximately 15-20 minutes per participant)
|
Muscle Activation Timing (%MVIC)
|
Single session (approximately 15-20 minutes per participant)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
April 20, 2026
Primary Completion (Estimated)
May 2, 2026
Study Completion (Estimated)
May 15, 2026
Study Registration Dates
First Submitted
April 9, 2026
First Submitted That Met QC Criteria
April 9, 2026
First Posted (Actual)
April 16, 2026
Study Record Updates
Last Update Posted (Actual)
April 16, 2026
Last Update Submitted That Met QC Criteria
April 9, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025/029
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data will not be shared to protect participant privacy and confidentiality.
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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