Clinical research and objective evaluation of the superior effect intervention of the non-drug characteristic treatment of chronic fatigue syndrome
- Conditions
- chronic fatigue syndrome
- Registration Number
- ITMCTR2000003947
- Lead Sponsor
- Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Chinese Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
According to the CFS diagnostic criteria established by the Centers for Disease Control and Prevention (CDC) in 1994, it meets the
a) Long-term or recurrent fatigue, lasting more than 6 months;
b) According to medical history, physical signs or laboratory test results, various organic diseases that cause chronic fatigue can be ruled out.
And have at least 4 of the following 8 items at the same time:
1) Short-term memory loss or inability to concentrate;
2) Sore throat;
3) Pain in lymph nodes;
4) Muscle aches;
5) Joint pain without redness and swelling;
6) New headache;
7) The energy cannot be recovered after sleep;
8) Consecutive 24 hours of physical discomfort after physical or mental work.
Subjects who meet any of the following will not be included in the group:
1) There is no chief complaint of fatigue, or fewer than 4 accompanying symptoms;
2) The fatigue symptoms can be relieved after rest;
3) The fatigue symptoms do not cause a substantial decrease in work ability, ability to receive education, social activities and entertainment activities, and personal life ability;
4) Suffer from tumor, diabetes, rheumatism and other diseases that can clearly cause fatigue;
5) Patients with severe heart, lung, liver, and kidney function abnormalities, and patients with abnormal thyroid function;
6) Patients with mental illness;
7) Women during pregnancy and lactation;
8) Adopt drug and non-drug treatment within 7 days before enrollment;
9) At the same time participating in other clinical trials.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Child Fatigue Scale;
- Secondary Outcome Measures
Name Time Method Interleukin;Tumor necrosis factor-a;Quality of life scale;C reactive protein;Brief Profile Of Mood States;Blood immunoglobulin;Blood cortisol;Pittsburgh Sleep Quality Index;gamma interferon;Blood lactic acid;