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The BSHAPE Intervention Program for Safety and Health of Survivors of Cumulative Trauma (BSHAPE)

Primary Purpose

Violence, Cumulative Trauma, HIV Risk

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
The BSHAPE Intervention
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Violence

Eligibility Criteria

18 Years - 55 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • 18-55 years of age
  • Self-identify as a female
  • Born in Africa or foreign born from African descent
  • Must have a current or past abusive romantic relationship
  • Must be a survivor of cumulative trauma
  • Clinically significant symptoms of PTSD and/or depression
  • At least one sexual HIV risk behavior

Exclusion Criteria:

  • Less than 18 years of age or more than age 55
  • Self-identify as a male
  • Not African-born immigrant or born outside the US
  • Is not a survivor of cumulative trauma
  • Does not meet clinically significant criteria of PTSD and/or depression
  • Does not report at least one sexual HIV risk behavior

Sites / Locations

  • Johns Hopkins University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

The BSHAPE Intervention

Usual care or no treatment control

Arm Description

Participants in the BSHAPE intervention attend a 9 sessions program post-assessments which is a combination of individualized and group-based sessions.

Participants in the control arm either are receiving no services or are engaged in usual care provided by community-based/health care organizations

Outcomes

Primary Outcome Measures

Change in depressive symptoms
The Patient Health Questionnaire (PHQ-9) is a 9 item measure to assess depression symptoms based on the diagnostic criteria for major depressive disorder in the Diagnostic and Statistical Manual (DSM-IV). Each of the 9 items scores from 0 (not at all) to 3 (nearly every day).
Change in symptoms of post-traumatic stress disorder (PTSD)
Harvard Trauma Questionnaire (16 items) is used to measure symptoms of PTSD derived from the DSM-IIR/DSM-IV criteria for PTSD. The scale for each question includes four categories of response: "Not at all," "A little," "Quite a bit," "Extremely," rated 1 to 4, respectively
Change in perceived stress
The Perceived stress scale is a 10 item self-report measure of stress. It is designed to assess how stressed one feels in the past month. Item responses are rated on a 5-point scale ranging from 0 (Never) to 4 (Very often). Higher scores indicate higher perceived stress. This scale is scored by summing the answers to all items, for a highest score of 40. Scores 0-13 indicate low stress, 14-26 is moderate stress and 27-40 is considered high stress.
Change in sexual risk behaviors
The Safe Sex Behavior Questionnaire is a 27-item self-report measure that describes sexual behaviors such as condom usage, sexual communication, and high-risk sexual behaviors. Item responses are rated on a 4-point scale ranging from 1 (Never) to 4 (Always). There are no subscales, and all items are summed to create a total score. Higher scores indicate engagement in safer sexual behaviors
Change in empowerment related to safety as assessed by the MOVERS scale
The MOVERS is a 13 item scale that measures empowerment within the domain of safety. Participants respond to each item using a five-point scale from 1- "never true" to 5 - "always true". A maximum total of 65 and minimum of 13. Higher scores indicate higher level of empowerment related to safety.

Secondary Outcome Measures

Change in overall empowerment as assessed by the Personal Progress Scale-Revised
The Personal Progress Scale-Revised is a 28 item self-report measure of empowerment designed to assess multiple areas associated with empowerment such as positive self-evaluation, self-esteem, ability to regulate emotional distress, gender-role and cultural identity awareness, self-efficacy, self-care, problem-solving, assertiveness skills, and access to resources. Item responses are rated on a 7-point scale ranging from 1 (Almost Never) to 7 (Almost Always). A total maximum composite score of 196 and a minimum of 28. Higher scores indicate higher level of empowerment.
Change in self-efficacy related to coping with trauma as assessed by the Trauma Coping Self-Efficacy scale
The Trauma Coping Self-Efficacy scale is a 9-item self-report scale aimed at assessing the belief in one's ability to cope with trauma. Items are rated in a 7-point scale ranging from 1 (Not at all capable) to 7 (Totally capable). All items are averaged, for a high score of seven. Higher scores indicate greater trauma coping self-efficacy.
Change in self-efficacy for HIV/Sexually Transmitted Infection (STI) prevention as assessed by the Self-Efficacy for STI-HIV Scale
The Self-Efficacy for STI-HIV Scale measures an individual's perceived ability to practice STD and HIV prevention strategies. The measure consists of 10 self-report items which are rated on a 5-point scale ranging from 1 (Not Sure) to 5 (Completely sure). All items are summed for a total score that can range from 10-50 with higher scores indicating higher self-efficacy.
Change in HIV knowledge using the HIV Knowledge Questionnaire
The HIV Knowledge Questionnaire is a 18-item self report measure designed to measure ones understanding of HIV transmission and prevention. Items are scored in a true-false format where one point is awarded for a correct answer. Incorrect answers and "don't know" is scored as zero. Items are summed for a total possible score of 18. Higher scores indicate greater knowledge about how HIV is transmitted and how it can be prevented.
Change in Sexually Transmitted Disease (STD) knowledge using the STD Knowledge Questionnaire
The STD Knowledge Questionnaire is a 27-item self-report measure designed to assess knowledge of transmission and prevention of common STDs such as Gonorrhea, Chlamydia, Hepatitis B, Human Papilloma Virus (HPV), and Genital Warts. Items are scored on a true-false scale where one point is awarded for each correct response. No points are given for incorrect responses or "Don't know". Items are summed to create a highest possible score of 27, with higher scores indicating high knowledge of how to prevent and transmit STDs.
Change in attitudes for stress management as assessed by the Inventory of Positive Psychological Attitudes
The Inventory of Positive Psychological Attitudes measures attitudes in different domains that can act as buffers to prevent stress and stress-related disorders. The 15 items measuring confidence during stress is used which measures one's ability to handle difficult times will be used. Item responses are scored on a 7-point scale ranging from 1 to 7 with a maximum total of 105 and a minimum of 7. Higher scores indicate greater resiliency.
Change in utilization of healthcare services
The Health Care Utilization measure was adapted from the Women's Health Care Experiences Survey. This measure was created as a self-report measure to capture women's use of different health care related services such as physical checkups, HIV screening, family planning services, abortion services, and other healthcare needs. For each different category of service, the measure asks if the service was used, where the service was received, if the service is available and why it was not used (if applicable). Each service is treated as a separate question, providing unique data; no scores are summed or averaged.
Change in severity and frequency of violence
The adapted version of the revised Conflict Tactics Scale (CTS) will be used to measure change in exposure to violence. The items on the CTS-2 are scored using the severity-times-frequency weighted score, as recommended by Straus (2004).
Change in physiological stress responses
Saliva samples are used to measure change in physiological stress response

Full Information

First Posted
September 4, 2018
Last Updated
May 25, 2023
Sponsor
Johns Hopkins University
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT03664362
Brief Title
The BSHAPE Intervention Program for Safety and Health of Survivors of Cumulative Trauma
Acronym
BSHAPE
Official Title
Cumulative Victimization and Women's Health Risks: Development of an Intervention
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
October 10, 2018 (Actual)
Primary Completion Date
February 19, 2022 (Actual)
Study Completion Date
February 19, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of the BSHAPE study is to test a trauma informed, culturally tailored, multicomponent program entitled BSHAPE (Being Safe, Healthy, And Positively Empowered) for immigrant survivors of cumulative trauma.
Detailed Description
The central hypothesis is that the BSHAPE intervention will promote immigrant women's safety and health (e.g..,improved mental health, reduced physiological impact of stress and health inequities (especially reproductive-sexual health and HIV)), thus leading to overall empowerment. The study will: Conduct a feasibility and acceptability evaluation of the BSHAPE intervention. Test the BSHAPE intervention for large scale implementation in community-based clinics and programs serving immigrant women. The impact of BSHAPE will be evaluated in comparison to usual care in promoting safety and health outcomes among immigrant women with cumulative trauma experiences at post-intervention and at 6 and 12 months follow up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Violence, Cumulative Trauma, HIV Risk, Stress, Mental Health, Reproductive Health, Empowerment

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
144 (Actual)

8. Arms, Groups, and Interventions

Arm Title
The BSHAPE Intervention
Arm Type
Experimental
Arm Description
Participants in the BSHAPE intervention attend a 9 sessions program post-assessments which is a combination of individualized and group-based sessions.
Arm Title
Usual care or no treatment control
Arm Type
No Intervention
Arm Description
Participants in the control arm either are receiving no services or are engaged in usual care provided by community-based/health care organizations
Intervention Type
Behavioral
Intervention Name(s)
The BSHAPE Intervention
Intervention Description
The BSHAPE intervention program key elements include strengths based assessments, individualized plans and support based on priorities and needs, motivational interviewing strategies, psychoeducation (education with skill building exercises), mindfulness activities, danger assessment, safety planning, behavioral activation and linkage to community resources
Primary Outcome Measure Information:
Title
Change in depressive symptoms
Description
The Patient Health Questionnaire (PHQ-9) is a 9 item measure to assess depression symptoms based on the diagnostic criteria for major depressive disorder in the Diagnostic and Statistical Manual (DSM-IV). Each of the 9 items scores from 0 (not at all) to 3 (nearly every day).
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Title
Change in symptoms of post-traumatic stress disorder (PTSD)
Description
Harvard Trauma Questionnaire (16 items) is used to measure symptoms of PTSD derived from the DSM-IIR/DSM-IV criteria for PTSD. The scale for each question includes four categories of response: "Not at all," "A little," "Quite a bit," "Extremely," rated 1 to 4, respectively
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Title
Change in perceived stress
Description
The Perceived stress scale is a 10 item self-report measure of stress. It is designed to assess how stressed one feels in the past month. Item responses are rated on a 5-point scale ranging from 0 (Never) to 4 (Very often). Higher scores indicate higher perceived stress. This scale is scored by summing the answers to all items, for a highest score of 40. Scores 0-13 indicate low stress, 14-26 is moderate stress and 27-40 is considered high stress.
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Title
Change in sexual risk behaviors
Description
The Safe Sex Behavior Questionnaire is a 27-item self-report measure that describes sexual behaviors such as condom usage, sexual communication, and high-risk sexual behaviors. Item responses are rated on a 4-point scale ranging from 1 (Never) to 4 (Always). There are no subscales, and all items are summed to create a total score. Higher scores indicate engagement in safer sexual behaviors
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)]
Title
Change in empowerment related to safety as assessed by the MOVERS scale
Description
The MOVERS is a 13 item scale that measures empowerment within the domain of safety. Participants respond to each item using a five-point scale from 1- "never true" to 5 - "always true". A maximum total of 65 and minimum of 13. Higher scores indicate higher level of empowerment related to safety.
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Secondary Outcome Measure Information:
Title
Change in overall empowerment as assessed by the Personal Progress Scale-Revised
Description
The Personal Progress Scale-Revised is a 28 item self-report measure of empowerment designed to assess multiple areas associated with empowerment such as positive self-evaluation, self-esteem, ability to regulate emotional distress, gender-role and cultural identity awareness, self-efficacy, self-care, problem-solving, assertiveness skills, and access to resources. Item responses are rated on a 7-point scale ranging from 1 (Almost Never) to 7 (Almost Always). A total maximum composite score of 196 and a minimum of 28. Higher scores indicate higher level of empowerment.
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Title
Change in self-efficacy related to coping with trauma as assessed by the Trauma Coping Self-Efficacy scale
Description
The Trauma Coping Self-Efficacy scale is a 9-item self-report scale aimed at assessing the belief in one's ability to cope with trauma. Items are rated in a 7-point scale ranging from 1 (Not at all capable) to 7 (Totally capable). All items are averaged, for a high score of seven. Higher scores indicate greater trauma coping self-efficacy.
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)]
Title
Change in self-efficacy for HIV/Sexually Transmitted Infection (STI) prevention as assessed by the Self-Efficacy for STI-HIV Scale
Description
The Self-Efficacy for STI-HIV Scale measures an individual's perceived ability to practice STD and HIV prevention strategies. The measure consists of 10 self-report items which are rated on a 5-point scale ranging from 1 (Not Sure) to 5 (Completely sure). All items are summed for a total score that can range from 10-50 with higher scores indicating higher self-efficacy.
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Title
Change in HIV knowledge using the HIV Knowledge Questionnaire
Description
The HIV Knowledge Questionnaire is a 18-item self report measure designed to measure ones understanding of HIV transmission and prevention. Items are scored in a true-false format where one point is awarded for a correct answer. Incorrect answers and "don't know" is scored as zero. Items are summed for a total possible score of 18. Higher scores indicate greater knowledge about how HIV is transmitted and how it can be prevented.
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Title
Change in Sexually Transmitted Disease (STD) knowledge using the STD Knowledge Questionnaire
Description
The STD Knowledge Questionnaire is a 27-item self-report measure designed to assess knowledge of transmission and prevention of common STDs such as Gonorrhea, Chlamydia, Hepatitis B, Human Papilloma Virus (HPV), and Genital Warts. Items are scored on a true-false scale where one point is awarded for each correct response. No points are given for incorrect responses or "Don't know". Items are summed to create a highest possible score of 27, with higher scores indicating high knowledge of how to prevent and transmit STDs.
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Title
Change in attitudes for stress management as assessed by the Inventory of Positive Psychological Attitudes
Description
The Inventory of Positive Psychological Attitudes measures attitudes in different domains that can act as buffers to prevent stress and stress-related disorders. The 15 items measuring confidence during stress is used which measures one's ability to handle difficult times will be used. Item responses are scored on a 7-point scale ranging from 1 to 7 with a maximum total of 105 and a minimum of 7. Higher scores indicate greater resiliency.
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Title
Change in utilization of healthcare services
Description
The Health Care Utilization measure was adapted from the Women's Health Care Experiences Survey. This measure was created as a self-report measure to capture women's use of different health care related services such as physical checkups, HIV screening, family planning services, abortion services, and other healthcare needs. For each different category of service, the measure asks if the service was used, where the service was received, if the service is available and why it was not used (if applicable). Each service is treated as a separate question, providing unique data; no scores are summed or averaged.
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Title
Change in severity and frequency of violence
Description
The adapted version of the revised Conflict Tactics Scale (CTS) will be used to measure change in exposure to violence. The items on the CTS-2 are scored using the severity-times-frequency weighted score, as recommended by Straus (2004).
Time Frame
Through study completion, an average of 1 year (Assessment time points: Baseline, 3 months, 6 months, 12 months)
Title
Change in physiological stress responses
Description
Saliva samples are used to measure change in physiological stress response
Time Frame
Assessment time points, Baseline, 3 months and 6 months

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
If identify as biologically female or transgender female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18-55 years of age Self-identify as a female Born in Africa or foreign born from African descent Must have a current or past abusive romantic relationship Must be a survivor of cumulative trauma Clinically significant symptoms of PTSD and/or depression At least one sexual HIV risk behavior Exclusion Criteria: Less than 18 years of age or more than age 55 Self-identify as a male Not African-born immigrant or born outside the US Is not a survivor of cumulative trauma Does not meet clinically significant criteria of PTSD and/or depression Does not report at least one sexual HIV risk behavior
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bushra Sabri, PhD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins University
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21205
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified individual participant data for all primary and secondary outcome measures will only be available to the research team members of the project
IPD Sharing Time Frame
Data will only be available for the duration of the project and one year after completion
IPD Sharing Access Criteria
The de-identified data will only be shared on a secure encrypted website that is managed by Johns Hopkins University
Citations:
PubMed Identifier
34626840
Citation
Sabri B, Vroegindewey A, Hagos M. Development, feasibility, acceptability and preliminary evaluation of the internet and mobile phone-based BSHAPE intervention for Immigrant survivors of cumulative trauma. Contemp Clin Trials. 2021 Nov;110:106591. doi: 10.1016/j.cct.2021.106591. Epub 2021 Oct 7.
Results Reference
derived

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The BSHAPE Intervention Program for Safety and Health of Survivors of Cumulative Trauma

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