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The Acupuncture Treatment Effect in Patients With Schizophrenia

The Quality of Life of Acupuncture Treatment Effect in Patients With Schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07351240
Enrollment
100
Registered
2026-01-20
Start date
2025-12-16
Completion date
2026-09-30
Last updated
2026-01-22

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

Conditions

Mental Health

Keywords

schizophrenia patients, acupuncture, antipsychotic side effects, psychiatric symptoms

Brief summary

Among various psychiatric disorders, this study focuses specifically on patients with schizophrenia. The aim of this study is to evaluate the therapeutic effects of acupuncture on antipsychotic medication-related side effects and psychiatric symptoms in patients with schizophrenia. This is a single-blind randomized study. Participants will be randomly assigned to one of two groups: Neiguan and Shenmen. Both the Neiguan and Shenmen groups will receive acupuncture treatment twice weekly, with each session lasting 30 minutes, for a total of four consecutive weeks. Assessments will be conducted prior to acupuncture intervention and after each acupuncture session. All assessment data will be collected and analyzed using statistical methods including descriptive statistics, chi-square tests, and t-tests. Generalized Estimating Equations (GEE-I) and multiple linear regression analyses will be applied to examine differences in psychological health, quality of life, and happiness before and after acupuncture intervention. It is anticipated that acupuncture will reduce antipsychotic-related side effects, improve psychiatric symptoms in patients with schizophrenia, and subsequently enhance patients' quality of life and happiness.

Interventions

OTHERAcupuncture

Both the Neiguan and Shenmen groups will receive acupuncture treatment twice weekly, with each session lasting 30 minutes, for a total of four consecutive weeks. Assessments will be conducted prior to acupuncture intervention and after each acupuncture session.

Sponsors

Calo Psychiatric Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

Participants will be randomly assigned to either the Neiguan group or the Shenmen group.

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of schizophrenia according to DSM-5 criteria for at least six months * Personal and Social Performance Scale score ≥ 50

Exclusion criteria

* Severe medical illnesses (e.g., cancer, chronic liver disease, renal failure) * History of stroke or other causes of hemiplegia * Severe dermatological disease or limb edema * High risk of violence or suicide * Alcohol or substance abuse or dependence * Severe cognitive impairment * Pregnancy or breastfeeding * Severe hepatic, renal, cardiac, pulmonary, or hematological disease * Major infectious diseases (e.g., HIV infection) * Refusal to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Hamilton Anxiety Scale15 minutesassess the anxiety state
Hamilton Depression Scale15-20 minutesassess the depression state
Short Version of the Udvalg for Kliniske Undersøgelser Side Effect Rating Scale5-10 minutesassess the psychiatric symptoms

Secondary

MeasureTime frameDescription
Happiness Scale5 minutesassess the happiness state

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026