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Clinical research on plastering acupoint with Daoyin in treatment of Chronic Fatigue Syndrome

Clinical research on plastering the acupoint with Daoyin in treatment of Chronic Fatigue Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001382
Enrollment
Unknown
Registered
2011-06-10
Start date
2010-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Chronic Fatigue Syndrome

Interventions

Group A:plaster the acupoint with Daoyin
Group B:plaster the acupoint
Group C:plaster the acupoint

Sponsors

Yueyang Hospital of Integrated Chinese Medicine and Western Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male and female aged 18 to 70 years old; 2. Meet diagnostic criteria of CFS; 3. Pathogenesis with "liver depression and spleen deficiency" in TCM; 4. Able and willing to provide signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Presence serious damage to heart, liver or kidney; 2. Presence blood disorders, Respiratory system disease, and severe mental illness; 3. Presence liver disease, AIDS or other infectious disease and serious injury which is not recovered; 4. Presence severe Digestive system disease and malnutrition; 5. Presence clear conditions known to cause fatigue; 6. Pregnant or lactating women; 7. lack of ability to comply by the protocol.

Design outcomes

Primary

MeasureTime frame
Fatigue questionnaire-14; Surface electromyogram median frequency; Peak torque; Average power; TW;the MOS item short from health survey, SF-36; Pittsburgh sleep quality index, PSQI; Serotonin; Cortisol;—

Countries

China

Contacts

Public ContactYunfei Chen
icyf1968@yahoo.com.cn+86 021 65161728-2629

Outcome results

None listed

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