Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:48 PM
Ignite Modification Date:
2025-12-24 @ 11:48 PM
NCT ID:
NCT07268651
Eligibility Criteria:
Inclusion Criteria:
* Adults aged 18-40 years who have undergone primary unilateral anterior cruciate ligament reconstruction (ACLR) using an autograft.
* At least 3 weeks postoperatively and currently engaged in the early-stage rehabilitation phase following ACLR.
* Demonstrate near-full passive knee extension (≤ 5° loss) and at least 90° of passive knee flexion in the operated limb.
* Able to walk independently without assistive devices and perform basic functional tasks (e.g., normal walking, single-leg stance).
* No prior surgery or major injury to the contralateral knee or other lower limb joints.
* No neurological, vestibular, or systemic conditions affecting proprioception, motor control, or physical performance.
* Not currently participating in any structured proprioceptive or neuromuscular training programs.
* Willing and able to comply with the intervention protocol and follow-up, and able to provide written informed consent.
Exclusion Criteria:
* History of revision anterior cruciate ligament surgery, bilateral ACLR, or concurrent reconstruction of other knee ligaments (e.g., posterior cruciate ligament, medial collateral ligament, lateral collateral ligament) in the affected knee.
* Meniscal repair or other intra-articular procedures that restrict knee range of motion beyond 3 weeks postoperatively.
* Diagnosed osteoarthritis, rheumatoid arthritis, or other chronic joint diseases affecting the lower limbs.
* Significant injury, surgery, or persistent pain in the contralateral knee, hip, ankle, or spine that could interfere with training or gait.
* History or current diagnosis of neurological disorders (e.g., stroke, multiple sclerosis, Parkinson's disease) or vestibular dysfunction.
* Any cardiopulmonary or systemic condition that contraindicates structured physical exercise.
* Participation in other structured rehabilitation or proprioceptive training programs within the past 3 weeks.
* Cognitive impairment or psychiatric conditions that may interfere with understanding instructions or complying with the protocol.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT07268651
Study Brief:
Protocol Section:
NCT07268651