NCT05940129

Brief Summary

Gender-based violence (GBV) (including homicide) is one of the leading causes of maternal and child (fetus, newborn or infant) mortality and morbidity in limited resource settings such as India. This study is evaluating the feasibility, acceptability and preliminary efficacy of WC-SHE (Women and Children-Safety, Health and Empowerment) intervention developed to promote health and safety outcomes of mother and children in rural and/or tribal regions in India. The aim will be to refine, optimize and standardize the WC-SHE intervention and its added components, develop fidelity measures, conduct a feasibility and acceptability evaluation of the intervention and implementation procedures as well as examine preliminary efficacy outcomes of WC-SHE.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 21, 2022

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

June 28, 2023

Completed
13 days until next milestone

First Posted

Study publicly available on registry

July 11, 2023

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2023

Completed
Last Updated

December 14, 2023

Status Verified

December 1, 2023

Enrollment Period

1.1 years

First QC Date

June 28, 2023

Last Update Submit

December 7, 2023

Conditions

Outcome Measures

Primary Outcomes (11)

  • Severity and frequency of abuse by husband and in-laws as measured by the adapted Conflict Tactics Scale (CTS2)

    Severity and frequency of abuse is assessed by the adapted version of the Revised Conflict Tactics Scale . Response categories range from 0 (never) to very 7 (frequently). Higher overall scores mean more conflict. Measured at Baseline, 3 months, 6 months.

    Baseline, 3 months, 6 months

  • Number of maternal safety behaviors as assessed by the Safety Behavior Checklist

    The Safety Behavior Checklist is used to measure the number of safety strategies and support services used. Measured at Baseline, 3 months, 6 months.

    Baseline, 3 months, 6 months

  • Victim empowerment related to safety as assessed by the Measure of Victim Empowerment Related to Safety (MOVERS) Scale

    The MOVERS scale is a 13 item scale that measures survivor empowerment within the domain of safety. Participants respond to each item using a five-point Likert scale (from "never true" to "always true. Possible score range 13-65. Higher scores indicate higher levels of empowerment related to safety. Measured at Baseline, 3 months, 6 months.

    Baseline, 3 months, 6 months

  • Uncertainty in choosing safety options as assessed by the Adapted Decisional Conflict scale

    The Adapted decisional conflict scale is used to measure decisional conflict for safety. The response options ranged from strongly disagree to strongly agree, with higher scores indicating lower decisional conflict. Decisional Conflict Scale scores range from 0(no decisional conflict) to 100 (high decisional conflict). Measured at Baseline, 3 months, 6 months.

    Baseline, 3 months, 6 months

  • Depression as assessed by the Patient Health Questionnaire

    The Patient Health Questionnaire (PHQ-9) is used to measure depression; Total scores of 5, 10, 15, and 20 represent cut points for mild, moderate, moderately severe and severe depression. Score range 0-27. Measured at Baseline, 3 months, 6 months.

    Baseline, 3 months, 6 months

  • Probable Post Traumatic Stress Disorder (PTSD) in primary care settings

    Primary Care PTSD Screen is a 5 item screen used to identify participants with probable PTSD in primary care settings. The items are rated on a binary scale (No, Yes). Score range 1-5. Higher scores indicate increased post traumatic stress symptoms. Measured at Baseline, 3 months, 6 months.

    Baseline, 3 months, 6 months

  • Physical health status

    For self-rated physical health, participants are asked about how would they describe their health during pregnancy (or post-delivery). The response options include poor, fair and excellent with poor coded as 1, fair as 2 and excellent as 3. Measured at Baseline, 3 months, 6 months.

    Baseline, 3 months, 6 months

  • Fetal safety as measured by occurrence of fetal loss

    Fetal loss includes post-intervention occurrence of any induced abortion or miscarriage, spontaneous abortion or miscarriage, or occurrence of fetal mortality or still birth

    Post intervention up to 6 months

  • Newborn/infant safety as measured by self-reported items developed by the study team

    The following items are used to measure newborn or infant safety, (a) participants are asked about concern for the child's mistreatment by the participants husband or in-laws. The response options range from never (0) to always (4). (b) Participants are asked if there is concern about harm to the child by anyone, with yes/no response options; Any incident of death of a child within few weeks post-delivery is based on participants' self-reports

    6 months

  • Newborn/infant health as measured by two items developed by the study team

    Newborn/infant health is measured by number of participants who delivered a low birth weight or pre-term child. Participants are asked if newborn was (a) a low birthweight child; and (b) child born preterm.

    6 months

  • Level of satisfaction with child's health and health-related issues as assessed by the Postpartum Quality of Life (PQOL) measure

    Participants are asked adapted items from the child care dimension of the Postpartum Quality of Life (PQOL) measure. The response options for items range from very dissatisfied to very satisfied and frequency levels ranging from never to always. Score range 16-80, with higher scores showing better quality of life.

    6 months

Secondary Outcomes (5)

  • Self-efficacy for safety as assessed by an item developed by study team

    Baseline, 3 months, 6 months

  • Resilience as assessed by the Connor Davidson Resilience Scale

    Baseline, 3 and 6 months

  • Sources of support as assessed by the Brief Perceived Social Support Questionnaire

    Baseline, 3 months, 6 months

  • Number of Self- care behaviors as measured by the items developed by the study team

    Baseline, 3 months, 6 months

  • Economic stress

    Baseline, 3 months, 6 months

Study Arms (3)

Web-based Intervention Arm (WC-SHE)

EXPERIMENTAL

Women in computerized WC-SHE arm receives education on healthy relationships the danger assessment and tailored safety planning and list of resources. The intervention also includes assessments of strengths and safety strategies. In addition, husbands and in-laws receive one-on-one health education session that includes topics related to maternal and child health and safety

Behavioral: Women and Child, Safety, Health and Empowerment (WC-SHE)

WC-SHE +Economic Empowerment

EXPERIMENTAL

Women in economic empowerment arm receive computerized WC-SHE and are connected with self-help groups. Husbands are also engaged in economic empowerment activities that involve individual psychoeducation, working with spouses in self-help group activities and participating in government economic or vocational training programs. In addition, husbands and in-laws participate in individual sessions on topics related to maternal and child health and safety

Behavioral: Women and Child, Safety, Health and Empowerment (WC-SHE)

WC-SHE + Enhanced Family Psychoeducation and Advocacy Support Intervention

EXPERIMENTAL

Women in this arm receive computerized WC-SHE, advocacy and support by a support committee of professionals based on women's priorities and needs, and phone call support by women community resource persons. Husbands and in-laws participate in individual and group sessions that cover topics such as stress, healthy relationships, healthy communication within families and impact of domestic violence on children.

Behavioral: Women and Child, Safety, Health and Empowerment (WC-SHE)

Interventions

The WC-SHE component includes a risk assessment and tailored safety planning for women in domestic violence relationships. In addition, the component involves one-on-one education with husbands and in-laws. The economic empowerment component is designed to support women and their husbands in economic empowerment activities. The advocacy arm involves community education of husbands and in-laws, advocacy support by a support committee comprised of multidisciplinary professionals and phone support by women community resource persons

WC-SHE + Enhanced Family Psychoeducation and Advocacy Support InterventionWC-SHE +Economic EmpowermentWeb-based Intervention Arm (WC-SHE)

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Over 18 years of age
  • Currently pregnant
  • Experienced intimate partner and/or in-law abuse in the past
  • Residing in rural or tribal areas in India

You may not qualify if:

  • Under 18 years of age
  • Not currently pregnant
  • No experience of intimate partner and/or in law abuse
  • Not residing in rural or tribal areas in India

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Johns Hopkins University

Baltimore, Maryland, 21205, United States

Location

MeSH Terms

Interventions

SafetyHealth

Intervention Hierarchy (Ancestors)

Accident PreventionAccidentsPublic HealthEnvironment and Public HealthPopulation Characteristics

Study Officials

  • Bushra Sabri, PhD

    Johns Hopkins University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 28, 2023

First Posted

July 11, 2023

Study Start

October 21, 2022

Primary Completion

November 30, 2023

Study Completion

November 30, 2023

Last Updated

December 14, 2023

Record last verified: 2023-12

Data Sharing

IPD Sharing
Will not share

Locations