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High-density electromyography study of muscle activation patterns with fascia compression band intervention

High-density electromyography study of muscle activation patterns with fascia compression band intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128002
Enrollment
Unknown
Registered
2026-07-13
Start date
2026-07-13
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Neuromuscular Function in Healthy Individuals

Interventions

The fascial compression band combined with active movement group:Under the condition of fascial compression band combined with active movement, the method of using the fascial compression band is the
Fascial compression band group:Under the condition of fascial compression band, the fascial compression band (Flossband Plum, length 3.5 meters, width 5 centimeters, produced by Sanctband Company in M
The active exercise group:Under the condition of act

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Healthy adults aged 18-35 years; 2. Have regular physical activity habits; 3. No known neurological, musculoskeletal, or upper extremity diseases; 4. Able to understand the research process and cooperate to complete the experimental tasks; 5. Voluntarily participated in this study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Had previous neurological disorders, musculoskeletal diseases or upper limb functional impairments; 2. Had upper limb-related musculoskeletal injuries within the past 6 months; 3. Was currently taking medications that might affect neuromuscular function; 4. Was allergic to latex or elastic band materials; 5. Had smoking, drinking or other behaviors during the study period that might affect neuromuscular function; 6. Was unable to complete the maximum voluntary contraction (MVC) and isometric contraction tasks; 7. Had other conditions that the researchers considered unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Motor unit discharge rate;Motor unit recruitment threshold;Motor unit derecruitment threshold;

Secondary

MeasureTime frame
Common synaptic input;Input–output gain of the motoneurons;

Countries

China

Contacts

Public ContactJiang Ning

West China Hospital of Sichuan University / Wearable Device Research Center of Sichuan University West China Hospital

ning.jiang@scu.edu.cn+86 28 8542 2654

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026