Depression Clinical Trial
Official title:
Transcutaneous Electrical Acupoint Stimulation (TEAS) and Dense Cranial Electroacupuncture Stimulation (DCEAS) for Psychiatric Sequelae and Related Biomarkers in Women Victims of Domestic Violence: a Randomized Controlled Trial
NCT number | NCT05102253 |
Other study ID # | UW 21-238 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | July 13, 2022 |
Est. completion date | December 2024 |
This is an assessor-blinded, randomized controlled trial. A total of 110 women victims of domestic violence aged 18-65 years will be recruited from local community centers and domestic violence shelters (refugee centers). They will be randomly assigned to routine care combined with (n = 55) and without (n = 55) additional acupuncture (TEAS+DCEAS) for 12 weeks. Acupuncture therapy will be conducted with 2 DCEAS sessions at clinics and 3 TEAS sessions at home each week. The primary outcome is the Beck Depression Inventory II (BDI-II) for depression. Secondary outcomes include the 17-item Hamilton Depression Rating Scale (HAMD-17) for depression, Perceived Stress Scale (PSS) for stress, PTSD Check List-Civilian Version (PCL-C) for PTSD symptoms, Insomnia Severity Index (ISI) for sleep and 12-Item Short Form Survey (SF-12) for quality of life. Two 10-ml blood samples will be drawn respectively at baseline and at the end of 12-week study. A generalized linear mixed-effect model will be applied to compare treatment outcomes over time in the two groups and linear regression will be conducted to examine inter-correlations among clinical improvement and changes in biomarker levels.
Status | Recruiting |
Enrollment | 110 |
Est. completion date | December 2024 |
Est. primary completion date | August 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Chinese women aged 18-65 years; - have experienced domestic violence in the previous two years, confirmed with the Abuse Assessment Screen (AAS) Screen Questionnaire; and - are currently experiencing a major depressive episode according to the criteria defined in the Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-5), with a BDI-II score of at least 14. Exclusion Criteria: - have serious medical conditions that may limit their participation in TEAS or DCEAS; - have a history of brain injury or surgery; - pregnancy or lactation; - have investigational drug treatment in the previous 6 months; - have heart pacemaker or other metal/electrical devices implanted in the body; or - have severe needle phobia. |
Country | Name | City | State |
---|---|---|---|
Hong Kong | The University of Hong Kong | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
The University of Hong Kong |
Hong Kong,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in Beck Depression Inventory-II (BDI-II) | BDI-II is used to measure the severity of depression. Higher scores indicate greater severity. Assessments will be conducted at baseline, week 3, week 6 and week 12. | Baseline, Week 3, Week 6 and Week 12 | |
Secondary | Changes in 17-item Hamilton Depression Rating Scale (HAMD-17) | HAMD-17 is used to measure the severity of depression. Higher scores indicate greater severity. Assessments will be conducted at baseline, week 3, week 6 and week 12. | Baseline, Week 3, Week 6 and Week 12 | |
Secondary | Changes in Perceived Stress Scale (PSS) | Stress is measured using PSS. Assessments will be conducted at baseline, week 3, week 6 and week 12. | Baseline, Week 3, Week 6 and Week 12 | |
Secondary | Changes in PTSD Check List-Civilian Version (PCL-C) | PTSD symptoms are measured using PCL-C. Assessments will be conducted at baseline, week 3, week 6 and week 12. | Baseline, Week 3, Week 6 and Week 12 | |
Secondary | Changes in Insomnia Severity Index (ISI) | Severity of insomnia are measured using ISI. Assessments will be conducted at baseline, week 3, week 6 and week 12. | Baseline, Week 3, Week 6 and Week 12 | |
Secondary | Changes in Pittsburgh Sleep Quality Index (PSQI) | Sleep quality is assessed using PSQI. Assessments will be conducted at baseline, week 3, week 6 and week 12. | Baseline, Week 3, Week 6 and Week 12 | |
Secondary | Changes in 12-Item Short Form Survey (SF-12) | Quality of life is measured using SF-12. Assessments will be conducted at baseline, week 3, week 6 and week 12. | Baseline, Week 3, Week 6 and Week 12 |
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