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Efficacy of Acupuncture at Acupoints Group Around the Base of Skull for Post-Stroke Depression

Post-stroke Depression Clinical Trial

Official title:
Efficacy of Acupuncture at Acupoints Group Around the Base of Skull for Post-Stroke Depression: a Randomized Controlled Trial

Clinical Trial Summary

The objective of this trial is to evaluate the efficacy and safety of electroacupuncture at acupoints group around the base of skull for post-stroke depression.

Clinical Trial Description

98 eligible participants with post-stroke depression will be recruited and randomly assigned to the experimental group and the control group in a ratio of 1:1. Participants in both groups will receive electroacupuncture or placebo acupuncture treatment at acupoints group around the base of skull 3 times a week for 4 weeks, and followed up for 24 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05310175
Study type Interventional
Source China Academy of Chinese Medical Sciences
Contact Yuxiao Zeng
Phone +86-15901278206
Email zengyuxiao@aliyun.com
Status Recruiting
Phase N/A
Start date May 6, 2022
Completion date October 2024
View Details
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