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The efficacy of feedback training combined with respiratory training in the treatment of peripheral nerve injury

The efficacy of feedback training combined with respiratory training in the treatment of peripheral nerve injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101829
Enrollment
Unknown
Registered
2025-04-30
Start date
2025-05-20
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

Peripheral nerve injury

Interventions

Respiratory training group:The ichoiceRelax intelligent decompression system produced by Beijing Chaosi Electronic Technology Co., Ltd. was used for respiratory training based on heart rate variabilit
Mirror-based myoelectric feedback set:Utilizing the Hobo HB120B myoelectric feedback electrical stimulator, myoelectric feedback intervention was performed with electrode pads placed at the muscles to

Sponsors

Tianjin Hospital, Tianjin City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Included based on symptoms, examination, by neurophysiological examination after referring to the diagnostic criteria of peripheral nerve injury in Practical Neurology 2. Age: 30-65 years old 3.Sunderland nerve grading: Grade II (nerve axon dissection, intact nerve lining and nerve bundle membrane) 4.Sensory hypersensitivity, peripheral numbness, pins and needles, and other sensory abnormalities. 5.Restriction of motor function and nerve reaction. 6. Voluntary participation in this experiment and ability to complete relevant experimental examinations. 7. Unilateral limb nerve injury 8. Pain intensity of 4-6 on a numerical rating scale

Exclusion criteria

Exclusion criteria: 1. Fracture did not heal 2. Any psychological or medical condition that may affect the patient's ability to adhere to the study protocol 3. The presence of massive venous thrombosis 4. Patients with visual perception disorders such as unilateral neglect or hemianopia 5. Severe hypertension (>= grade 2) 6. Patients with apraxia 7. Bed Angle <=45° 8. Cognitive and speech dysfunction 9. Patients and their families do not cooperate and cannot cooperate to complete the experiment 10. Patients with severe lung diseases (such as emphysema, severe asthma), epilepsy, tuberculosis or other infectious diseases, or prone to respiratory acidosis;

Design outcomes

Primary

MeasureTime frame
Root mean square amplitude of surface electromyography;Peripheral nerve conduction function (EMG);Pressure-pain threshold;Electroencephalography;Heart rate variability;

Secondary

MeasureTime frame
Muscle thickness and pinnation angle (musculoskeletal ultrasound);Range of motion;Two-point discrimination;Skin moisture;

Countries

China

Contacts

Public ContactQi Li

Tianjin Hospital, Tianjin City

Liqi_82@126.com+86 150 2209 5665

Outcome results

None listed

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