NCT07201597 Correlation Between Psychological Readiness, Knee Function, and Isokinetic Performance After Anterior Cruciate Ligament Reconstruction (ACLR) Using Peroneus Longus Tendon Graft (PL-ACL-2025)
| NCT ID | NCT07201597 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Cairo University |
| Condition | Anterior Cruciate Ligament (ACL) Injury |
| Study Type | OBSERVATIONAL |
| Enrollment | 52 participants |
| Start Date | 2025-10-08 |
| Primary Completion | 2025-11-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 52 participants in total. It began in 2025-10-08 with a primary completion date of 2025-11-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This clinical trial aims to investigate the correlation between psychological readiness, knee function, and isokinetic performance after anterior cruciate ligament reconstruction (ACLR) using the Peroneus Longus tendon graft (PLT). ACL injuries are common among athletes, and the standard treatment is ACL reconstruction surgery (ACLR). However, the success of the surgery does not solely depend on physical recovery but also on the psychological readiness of athletes to return to their sport. This study focuses on athletes who have undergone ACLR using the Peroneus Longus tendon (PLT). The primary objective is to compare psychological readiness, self-reported knee function (IKDC score), isokinetic performance (quadriceps and hamstring strength), and muscle strength ratios between athletes who meet return-to-sport (RTS) criteria and those who do not. Psychological readiness will be assessed using the ACL-Return to Sport after Injury (ACL-RSI) scale, while knee function will be evaluated using the IKDC subjective score. Isokinetic testing will assess quadriceps and hamstring strength at various angular velocities. This study aims to provide a more comprehensive understanding of the factors influencing an athlete's ability to return to sport after ACLR, combining both physical and psychological aspects. The results will help optimize rehabilitation strategies by offering a multidimensional approach, considering both physical and psychological factors, to improve recovery protocols for ACL-injured athletes.
Eligibility Criteria
Inclusion Criteria: * Male recreational athletes aged 18-35 years. * Participation in sports that involve deceleration, jumping, cutting, or turning (e.g., basketball, soccer, volleyball). * Primary unilateral ACL injury treated with ACL reconstruction using a Peroneus Longus autograft. * Single evaluation 6-12 months after ACL reconstruction. * Completed a standardized postoperative rehabilitation program for ≥6 months, with near-complete rehabilitation and some level of sport participation. * Sufficient knee confidence, no effusion/edema, full knee range of motion, and able to perform all functional tests safely. * Able to provide written informed consent. Exclusion Criteria: * Revision ACL reconstruction. * Prior ACL reconstruction on the ipsilateral or contralateral knee. * Multi-ligament knee injury. * Concomitant meniscal repair or bilateral ACL reconstruction. * Knee pain \> 3/10 at evaluation that prevents or impairs testing. * Incomplete knee extension or knee flexion \< 110°. * Lower-limb fracture or surgery within the past 6 months.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07201597 clinical trial?
This trial is open to male participants only, aged 18 Years or older, up to 35 Years, studying Anterior Cruciate Ligament (ACL) Injury. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07201597 currently recruiting?
Yes, NCT07201597 is actively recruiting participants. Contact the research team at hamdymostafa655@gmail.com for enrollment information.
Where is the NCT07201597 trial being conducted?
This trial is being conducted at Cairo, Egypt.
Who is sponsoring the NCT07201597 clinical trial?
NCT07201597 is sponsored by Cairo University. The trial plans to enroll 52 participants.