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Clinical Application Study of Central Stimulation Technology Combined with Non-conscious Proprioceptive Training in Chronic Ankle Instability

Clinical Application Study of Central Stimulation Technology Combined with Non-conscious Proprioceptive Training in Chronic Ankle Instability

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116801
Enrollment
Unknown
Registered
2026-01-15
Start date
2026-01-22
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Chronic Ankle Instability

Interventions

Non-conscious proprioceptive group:Non-conscious proprioceptive training
Central Stimulation Group:Central stimulation technology
Combined group:Central stimulation technology+Non-conscious proprioceptive training

Sponsors

Xuzhou Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. According to the screening criteria for chronic ankle instability proposed by the International Ankle Consortium, the patient was diagnosed with CAI. 2. Aged 18-60 years old, regardless of gender, with no sprain of ankle in the past month; no other treatments received in the past 3 months. 3. Unilateral injury of ankle; 4. The unaffected lower limb has no other diseases. 5. Good compliance, able to complete the training plan on schedule; 6. Irregular exercise habits; 7. Informed consent forms were signed prior to the experiments.

Exclusion criteria

Exclusion criteria: 1. Presence of other diseases causing abnormal walking function in Parazacco spilurus subsp. spilurus; 2. Severe combined pathological changes in vital organs such as heart, liver, lungs, and kidneys; 3. Pathological fracture, postoperative infection, combined with nerve injury; 4. Anterior drawer test, talar tilt test positive; 5. Having central nervous system or vestibular system disorders, as well as other conditions that may affect balance ability such as severe visual impairment (myopia exceeding 800 diopters in one eye). 6. Pregnant or lactating women; History of cardiac pacemakers, other metal implants, or contraindications to rTMS therapy; 7. Unable to cooperate with examination and treatment.

Design outcomes

Primary

MeasureTime frame
AOFAS Ankle-Hindfoot Scale;Near-infrared brain functional imaging;Three-dimensional gait analysis system;

Secondary

MeasureTime frame
Somatosensory evoked potential;

Countries

China

Contacts

Public ContactZhai Hongwei

Xuzhou Rehabilitation Hospital

zhw2625329@163.com+86 516 83726369

Outcome results

None listed

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