Acupuncture for Women Victims of Domestic Violence With Psychiatric Sequelae
Primary Purpose
Depression, Domestic Violence, Psychiatric Disorder
Status
Recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Dense cranial electroacupuncture stimulation (DCEAS)
Transcutaneous electrical acupoint stimulation (TEAS)
Wait-list control: Routine care
Sponsored by
About this trial
This is an interventional treatment trial for Depression focused on measuring Depression, Domestic Violence, Psychiatric Sequelae, Acupuncture, Transcutaneous Electrical Acupoint Stimulation, TEAS, Dense Cranial Electroacupuncture Stimulation, DCEAS
Eligibility Criteria
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.
Sites / Locations
- The University of Hong KongRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
TEAS+DCEAS group
Wait-list control: Routine care group
Arm Description
Subjects assigned to TEAS+DCEAS group will receive TEAS+DCEAS in addition to routine care.
Subjects assigned to this group will continue their current routine care as usual.
Outcomes
Primary Outcome Measures
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.
Secondary Outcome Measures
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.
Changes in Perceived Stress Scale (PSS)
Stress is measured using PSS. Assessments will be conducted at baseline, week 3, week 6 and week 12.
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.
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.
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.
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.
Full Information
NCT ID
NCT05102253
First Posted
September 27, 2021
Last Updated
October 31, 2022
Sponsor
The University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT05102253
Brief Title
Acupuncture for Women Victims of Domestic Violence With Psychiatric Sequelae
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
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 13, 2022 (Actual)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed Description
Domestic violence, also referred to as intimate partner violence which overwhelmingly targets women of marriage and cohabitation, is a serious global public health issue with nearly 30% of women who have experienced physical or sexual abuse by their intimate partners. In Hong Kong, there were 4.5%-10% of women who experienced a physical violence and approximately 14,000 domestic violence cases reported to police offices each year. Depression is the most common psychiatric sequela of domestic violence, with an average prevalence of 47.6% among women victims. Recent study has shown that 65.2% women survivors of intimate partner violence had mild to severe depression. Abused women also often experienced post-traumatic stress disorder (PTSD), anxiety, substance abuse, and even suicidal thoughts. Although multiple psychological therapies, such as advocacy, cognitive behavioral therapy (CBT), and empowerment are a mainstay of domestic violence victim interventions, a large portion of the victims could not achieve satisfactory response and have low acceptability for psychological interventions; this seems to be particularly apparent in Asian women. Psychological interventions may be limited to patients with mild symptoms with long-term engagement of professionals. The development of non-psychological therapies is therefore highly desired.
Acupuncture has been widely introduced into local clinics and hospitals of Hong Kong. Numerous studies have shown benefits and efficacy of acupuncture in the treatment of various psychiatric disorders, including depression and anxiety. In addition to traditional invasive acupuncture in which needles are inserted into acupoints on the body, a non-invasive acupuncture mode called transcutaneous electrical acupoint stimulation (TEAS) also has been used in the treatment of postoperative anxiety, depression, autism, smoking cessation, and drug dependence. Compared to invasive acupuncture, obviously, TEAS is more acceptable to patients and physicians as it is non-invasive, safer, and time-saving, without causing pain and needle phobia. Furthermore, TEAS can be performed by patients themselves at home. These suggest that a combination of invasive acupuncture and TEAS could serve as an effective and more acceptable intervention for the victims.
Over the past decade, the effectiveness of advocacy and Qigong interventions in domestic violence women victims has been evaluated. Also, investigators have completed a series of epidemiological and methodological studies on women victims of domestic violence in local and international communities, with over 30 related papers published. On the other hand, a novel acupuncture stimulation called dense cranial electroacupuncture stimulation (DCEAS) based on neuroanatomical rationales has been developed. In this mode, electrical stimulation is delivered on dense acupoints located on the forehead innervated by the trigeminal nerve. Several clinical trials have confirmed the benefits and efficacy of DCEAS in patients with depression, obsessive-compulsive disorder (OCD), and neuropsychiatric sequelae of stroke. Moreover, two large-scale clinical trials have shown that patients with OCD and PTSD achieved an approximately 20% higher clinical remission rate on TEAS combined with CBT and/or antidepressants than those without TEAS. These results provide a solid foundation for further evaluation of the effectiveness of combining TEAS and DCEAS.
Besides, preliminary study has shown that several blood biomarkers were significantly correlated with the severity of depression and stress trauma. Determining relationships between potential biomarkers and the severity of psychiatric symptoms will lead people to better understand the pathogenesis of stress trauma and biochemical mechanisms of acupuncture effects.
These studies have led us to hypothesize that additional therapy with a combination of TEAS and DCEAS produces better outcomes than routine care alone in improving depression and other psychiatric sequelae of domestic violence; the therapeutic effects of acupuncture may be associated with the change of related biomarkers.
To test this hypothesis, an assessor-blinded, randomized controlled trial will be conducted to pursue the following two aims: (1) to compare the effectiveness of routine care with and without additional acupuncture in treating depression, stress, PTSD, insomnia symptoms, and quality of life of domestic violence women victims; and (2) to determine baseline-to-endpoint changes in levels of different blood biomarkers and their correlations with clinical outcomes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Domestic Violence, Psychiatric Disorder
Keywords
Depression, Domestic Violence, Psychiatric Sequelae, Acupuncture, Transcutaneous Electrical Acupoint Stimulation, TEAS, Dense Cranial Electroacupuncture Stimulation, DCEAS
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
110 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
TEAS+DCEAS group
Arm Type
Experimental
Arm Description
Subjects assigned to TEAS+DCEAS group will receive TEAS+DCEAS in addition to routine care.
Arm Title
Wait-list control: Routine care group
Arm Type
Other
Arm Description
Subjects assigned to this group will continue their current routine care as usual.
Intervention Type
Procedure
Intervention Name(s)
Dense cranial electroacupuncture stimulation (DCEAS)
Intervention Description
DCEAS will be conducted for 2 sessions per week for 12 consecutive weeks. Electrical stimulation will be conducted on six pairs of forehead acupoints located on the frontal, parietal, and temporal scalp areas. The acupoints includes: Bai-Hui (GV20), Yin-Tang (EX-HN3), left and right Si-Shen-Cong (EX-HN1), Tou-Lin-Qi (GB15), Shuai-Gu (GB8), Tai-Yang (EX-HN5) and Tou-Wei (ST8).
Disposable acupuncture needles will be inserted at a depth of 10-30 mm perpendicularly or obliquely into acupoints. Manual manipulation will be carried out for all acupoints to evoke needling sensation, followed by electrical stimulation. The stimulation intensity will be adjusted to a level at which patients felt most comfortable. Each session of treatment will last 30 min.
Intervention Type
Procedure
Intervention Name(s)
Transcutaneous electrical acupoint stimulation (TEAS)
Intervention Description
TEAS will be done for 3 times per week for 12 consecutive weeks by participants at home. A training workshop will be conducted to instruct participants how to use TEAS stimulator. Briefly, TEAS will be delivered on the bilateral Nei-Guan (PC6), which is located on the anterior forearm, between the tendons of the palmaris longus and flexor carpi radialis, at the junction of the distal sixth and proximal five sixths of the line connecting the middle points of the wrist and elbow crease.
Constant current electrical impulses will be produced from a TEAS apparatus. Two electrode pads will be adhered onto the acupoint skin. The pulse amplitude will be adjusted to a level at which the perception of 'strong but comfortable' is achieved. Each session of treatment will last 30 min.
Intervention Type
Other
Intervention Name(s)
Wait-list control: Routine care
Intervention Description
The routine care may include medications, advocacy intervention, and CBT. Post-trial treatment of TEAS+DCEAS will be offered to serve as a compensation for their participation.
Primary Outcome Measure Information:
Title
Changes in Beck Depression Inventory-II (BDI-II)
Description
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.
Time Frame
Baseline, Week 3, Week 6 and Week 12
Secondary Outcome Measure Information:
Title
Changes in 17-item Hamilton Depression Rating Scale (HAMD-17)
Description
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.
Time Frame
Baseline, Week 3, Week 6 and Week 12
Title
Changes in Perceived Stress Scale (PSS)
Description
Stress is measured using PSS. Assessments will be conducted at baseline, week 3, week 6 and week 12.
Time Frame
Baseline, Week 3, Week 6 and Week 12
Title
Changes in PTSD Check List-Civilian Version (PCL-C)
Description
PTSD symptoms are measured using PCL-C. Assessments will be conducted at baseline, week 3, week 6 and week 12.
Time Frame
Baseline, Week 3, Week 6 and Week 12
Title
Changes in Insomnia Severity Index (ISI)
Description
Severity of insomnia are measured using ISI. Assessments will be conducted at baseline, week 3, week 6 and week 12.
Time Frame
Baseline, Week 3, Week 6 and Week 12
Title
Changes in Pittsburgh Sleep Quality Index (PSQI)
Description
Sleep quality is assessed using PSQI. Assessments will be conducted at baseline, week 3, week 6 and week 12.
Time Frame
Baseline, Week 3, Week 6 and Week 12
Title
Changes in 12-Item Short Form Survey (SF-12)
Description
Quality of life is measured using SF-12. Assessments will be conducted at baseline, week 3, week 6 and week 12.
Time Frame
Baseline, Week 3, Week 6 and Week 12
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhang-Jin Zhang, MMed, PhD
Phone
+852 3917 6445
Email
zhangzj@hku.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Sichang YANG
Phone
+852 65612746
Email
sichang@hku.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhang-Jin Zhang, MMed, PhD
Organizational Affiliation
School of Chinese Medicine, The University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Hong Kong
City
Hong Kong
ZIP/Postal Code
999077
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhang-Jin Zhang, MMed, PhD
Phone
+852 3917 6445
Email
zhangzj@hku.hk
12. IPD Sharing Statement
Plan to Share IPD
No
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Acupuncture for Women Victims of Domestic Violence With Psychiatric Sequelae
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