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Efficacy of Tecar Therapy Combined with Visual Feedback Balance Training in Postoperative Rehabilitation of Lateral Ankle Ligament Injuries

Efficacy of Tecar Therapy Combined with Visual Feedback Balance Training in Postoperative Rehabilitation of Lateral Ankle Ligament Injuries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110449
Enrollment
Unknown
Registered
2025-10-14
Start date
2025-10-20
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Ankle Ligament Injuries

Interventions

Control Group:Visual Feedback Balance Training Training was conducted using a balance function assessment and training system (Model: SY-PH710B), with the specific protocol as follows: Static Balance
coronal plane: -0° (inversion) ~ +15° (eversion)). Patients adjusted their body posture based on visual feedback to complete trajectory training. Each training session lasted 20 minutes, once a day, 5
Experimental group:Visual Feedback Balance Training: Same as the control group
TECAR Therapy: A radiofrequency physical therapy instrument (Model: XSSP-3SE, Tianjin Shunbo Medical Equipment) was used, with specific operations as follows: ? Electrode Selection: Two circular non-i
? Treatment Mode: Resistive mode (for ligament and tendon ti

Sponsors

Hubei Provincial Hospital of Integrated Traditional Chinese and Western Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1 .Meeting the diagnostic criteria for lateral ankle ligament injury, and having undergone lateral ligament repair/reconstruction surgery via arthroscopy or open surgery (2-4 weeks postoperatively, after wound healing and suture removal); 2.Aged 18-50 years; 3.Having obvious postoperative balance dysfunction (Berg Balance Scale [BBS] score = 3); 4.Having not received other physical factor therapy or balance training within the past month; 5. All patients receiving routine postoperative rehabilitation care for lateral ankle ligament injury (e.g., wound care, elevation of the affected limb, passive range-of-motion training for the ankle joint); 6. Having normal cognitive function (Mini-Mental State Examination [MMSE] score >= 27) and being able to cooperate with training and assessment; 7.Having signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Complicated with ankle fracture, cartilage injury (Outerbridge classification >= Grade III) or other ligament complex injuries; 2.Having severe cardiovascular diseases, coagulation disorders, or abnormal skin sensation (e.g., diabetic peripheral neuropathy); 3.Allergic to high-frequency current or having implanted metal foreign bodies in the body (e.g., cardiac pacemakers); 4. A history of previous ankle surgery or chronic instability; 5.Being pregnant or lactating women; 6.Severe internal diseases and related complications; 7.Having cognitive impairment, mental illness, or the like.

Design outcomes

Primary

MeasureTime frame
Ankle Proprioception;

Secondary

MeasureTime frame
Visual Analog Scale (VAS);Static Balance Function;Ankle Active Range of Motion (AROM);American Orthopaedic Foot and Ankle Society (AOFAS) Ankle-Hindfoot Scale;Assessment of Lower Limb Explosive Strength via Countermovement Jump (CMJ);Assessment of Lower Limb Motor Coordination via 5-Hop Test;

Countries

China

Contacts

Public ContactLi Kui

Hubei Provincial Hospital of Integrated Traditional Chinese and Western Medicine

529197140@qq.com+86 186 2780 8862

Outcome results

None listed

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