MedPath

Feasibility Study for Abused Chinese Immigrant Women

Not Applicable
Completed
Conditions
Anxiety
PTSD
Intimate Partner Violence
Depression
Interventions
Behavioral: The Control Condition
Behavioral: Self-Compassion, Health, and Empowerment (SHE)
Registration Number
NCT05011552
Lead Sponsor
University of Texas at Austin
Brief Summary

Intimate partner violence (IPV) is a serious social and public health issue. In the U.S., more than 1 in 3 women experience physical or sexual violence, and/or stalking by an intimate partner during their lifetime. IPV has significant physical and mental health consequences such as injury, chronic pain, and depression. Chinese immigrants have been overlooked and underserved and represent an especially vulnerable group of IPV victims, as they are less likely to seek help through IPV service agencies, women's shelters, hospitals, or law enforcement. Effective IPV intervention programs that are culturally appropriate, accessible, and acceptable are essential to this underserved population. However, no studies have been conducted with abused Chinese immigrant women to help them deal with IPV and reduce mental health consequences.

Therefore, the study adapted a structured IPV intervention from the Domestic Violence Enhanced Home Visitation Program (DOVE) as well as incorporate self-compassion and relaxation techniques for Chinese immigrant women experiencing IPV. The intervention is called Self-Compassion, Health, and Empowerment (SHE). The study will test the feasibility and acceptability of the SHE to reduce IPV and improve mental health well-being for abused Chinese immigrant women residing in the US.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
50
Inclusion Criteria
  • 18 years or older and female, self-identify as Chinese, reside in the U.S., have been in an intimate relationship at time of participation, and have experienced IPV within the current relationship.
Exclusion Criteria
  • Women are excluded if they report substance use or suicidality or having been in mental health care for severe mental illness.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
The control groupThe Control Condition-
The intervention groupSelf-Compassion, Health, and Empowerment (SHE)-
Primary Outcome Measures
NameTimeMethod
Intimate Partner ViolenceIt will be assessed 2 months after the 8-week intervention.

The Revised Conflict Tactics Scales (CTS2)

DepressionIt will be assessed 2 months after the 8-week intervention.

The Patient Health Questionnaire-9 (PHQ-9)

AnxietyIt will be assessed 2 months after the 8-week intervention.

The Generalized Anxiety Disorder-7 (GAD-7)

Posttraumatic Stress Disorder (PTSD)It will be assessed 2 months after the 8-week intervention.

The PTSD Checklist for DSM-5 (PCL-5)

Secondary Outcome Measures
NameTimeMethod
Self-CompassionIt will be assessed 2 months after the 8-week intervention.

The Self-Compassion Scale-Short Form (SCS-SF)

Number of Safety Behaviors Taken by ParticipantsIt will be assessed 2 months after the 8-week intervention.

The Intimate Partner Violence Strategies Index

Trial Locations

Locations (1)

The University of Texas At Austin

🇺🇸

Austin, Texas, United States

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