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Clinical Trial for Efficacy and Safety Evaluation of Neurostimulation using Electroacupuncture in Patients with Anxiety Disorder

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008378
Enrollment
60
Registered
2023-04-21
Start date
2022-12-15
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

None listed

Interventions

Others : Participants will be randomly assigned to PC6 electroacupuncture-median nerve stimulation (EA-MNS) group or TF4 electroacupuncture-vagus nerve stimulation (EA-VNS) group or usual care (UC) gr

Sponsors

Daejeon Korean Medicine Hospital of Daejeon University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria

Exclusion criteria: 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

Design outcomes

Primary

MeasureTime frame
Hamilton Anxiety Rating Scale

Secondary

MeasureTime frame
Beck Anxiety Inventory;Beck Depression Inventory;Patient Health Questionnaire-15;WHO QoL assessment instrument abbreviated version;Penn State Worry Questionnaire (only for Generalized anxiety disorder, Other specified anxiety disorders, Anxiety disorder, unspecified);The Panic Disorder Severity Scale (only for Panic disorder and Agoraphobia);Liebowitz Social Anxiety Scale (only for Social anxiety disorder)

Countries

Korea, Republic of

Contacts

Public ContactJieun Kim

Korea Institute of Oriental Medicine

jieunkim@kiom.re.kr+82-42-869-2799

Outcome results

None listed

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