Clinical Feasibility Evaluation of Electroacupuncture-Neural Stimulation in Patients with Anxiety Disorder: Randomized, Evaluator-blinded, Usual Care-Controlled Clinical Trial

Daejeon Korean Medicine Hospital of Daejeon University0 个研究点目标入组 60 人开始时间: 待定最近更新: 2023年5月2日

适应症

试验速览

暂无简介。

•Participants who
•1) aged 19-70 years old
•2) diagnosed of anxiety disorder by Structured Clinical Interview for DSM-5 including social anxiety disorder, agoraphobia, panic disorder, generalized anxiety disorder, other specified anxiety disorders and unspecified anxiety disorder
•3) voluntarily decide to participate in this clinical study and signed the written consent form
•4) are able to complete electroacupuntrue-neural stimulation treatments for 8 weeks

•1) risk of suicide with C-SSRS > 4
•2) current or past history of schizophrenia or bipolar disorder
•3) separation anxiety disorder, elective mutism, substance-induced anxiety disorder, anxiety disorder due to medication, or anxiety disorder due to other medical conditions
•4) history of acupuncture treatment within 4 weeks
•5) alcohol or other substance use disorders within 8 weeks
•6) history of cerebrovascular diseases, brain tumor, or traumatic brain injury
•7) history of neurological or systemic diseases that may affect central nervous system
•8) unstable medical conditions requiring inpatient treatment
•9) usage of a pacemaker
•10) indications for acupuncture treatment being inappropriate or unsafe (e.g., acupuncture-associated vasovagal response or tissue damage due to acupuncture)
•11) participation in medication or other intervention in other clinical trials within 1 month
•12) pregnant or lactating women or not using medically acceptable contraception during the study period
•13) inappropriate for enrollment due to other reasons as determined by the investigators

发起方

Daejeon Korean Medicine Hospital of Daejeon University