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Research on the Effects and Mechanisms of Different Attentional Focus Strategies on Neuromuscular Dysfunction After Anterior Cruciate Ligament Reconstruction Surgery.

Research on the Effects and Mechanisms of Different Attentional Focus Strategies on Neuromuscular Dysfunction After Anterior Cruciate Ligament Reconstruction Surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100381
Enrollment
Unknown
Registered
2025-04-08
Start date
2025-04-08
Completion date
Unknown
Last updated
2025-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior cruciate ligament injury

Interventions

The ACLR group and :None

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: ACLR Patients: 1.Age: 18-50 years old; 2.Injury type: Isolated anterior cruciate ligament (ACL) injury; 3.Postoperative time: 6-12 months after anterior cruciate ligament reconstruction (ACLR) surgery; 4.Tegner score: Tegner score before injury greater than 5; 5.Dominant limb: Right side; 6.Visual acuity: Normal vision or corrected to normal. Healthy Subjects: 1.Matched with the ACLR group in terms of age, height, weight, gender, dominant leg, and preoperative Tegner score at the group level.

Exclusion criteria

Exclusion criteria: ACLR Patients: 1.Have undergone more than one anterior cruciate ligament reconstruction surgery; 1.Have bilateral ACL injuries; 3.Have concomitant injuries to other knee or ankle joints; 4.Have a history of other lower limb surgeries; 5.Have diseases affecting balance ability, such as visual or vestibular dysfunction; 6.Have a history of neurological or psychiatric disorders; 7.Are currently taking medications that may affect cognition (e.g., antidepressants, anxiolytics, opioids, etc.); 8.Are unwilling to sign the informed consent form. Healthy Subjects: 1.Have had lower limb injuries or surgeries within the past month; 2.Have diseases affecting balance ability, such as visual or vestibular dysfunction; 3.Are unwilling to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Postural Control (Center of Pressure Variation);Cerebral Blood Flow Changes;Electromyographic (EMG) Changes;

Secondary

MeasureTime frame
Clinical indicators such as muscle strength, proprioception, etc.;

Countries

China

Contacts

Public ContactWeidong Xu

Shanghai Changhai Hospital

xuwdshanghai@126.com+86 139 0181 4702

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026