Skip to main content
Clinical Trials/ITMCTR2100004875
ITMCTR2100004875
Recruiting
Phase 1

Study on brain functional network of acupuncture point combination

Medical College of Acu-Moxi and Rehabilitation, Guangzhou University of Chinese Medicine0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Medical College of Acu-Moxi and Rehabilitation, Guangzhou University of Chinese Medicine
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Observational study
Sex
All

Investigators

Sponsor
Medical College of Acu-Moxi and Rehabilitation, Guangzhou University of Chinese Medicine

Eligibility Criteria

Inclusion Criteria

  • 1\. Self\-rating Depression Scale (SDS) \<53 points, and Self\-rating Anxiety Scale (SAS) \<50 points, and Pittsburgh Sleep Quality Index (PSQI) \<6 points, and Baker Depression Inventory (BDI\- II) \<14 points;
  • 2\. Hamilton Depression Scale (HAMD\-17\) score: HAMD total score \<7 points;
  • 3\. There is no restriction on gender, over 18 years old and under 55 years old;
  • 4\. Able to complete the questionnaire independently, with informed consent and voluntarily fill out.

Exclusion Criteria

  • 1\. Patients diagnosed with subliminal depression;
  • 2\. Suffer from serious heart, brain, liver, kidney, hematopoietic system and other diseases;
  • 3\. Women during pregnancy and lactation;
  • 4\. Depressive episodes caused by psychoactive substances and non\-addictive substances;
  • 5\. Take drugs or receive any treatment during the trial period;
  • 6\. Known alcohol abuse or substance dependence;
  • 7\. Participating in other clinical trials;
  • 8\. Those who have a lack of skull at the acupuncture site and scars from skin infections and surgery that affect the treatment;
  • 9\. Patients who are allergic to acupuncture or who have experienced fainting;
  • 10\. Those who are uncooperative or unable to effectively complete the test during the test.

Outcomes

Primary Outcomes

Not specified

Similar Trials