Dissemination and Implementation of a Web-based Relationship Safety App, myPlanKenya, for Women at Risk for Intimate Partner Violence in Nairobi, Kenya

Sponsor
Johns Hopkins Bloomberg School of Public Health (Other)
Overall Status
Recruiting
CT.gov ID
NCT05609786
Collaborator
Ujamaa Africa (Other)
400
1
1
29.5
13.5

Study Details

Study Description

Brief Summary

This effectiveness-implementation hybrid-3 study evaluates dissemination, implementation, and effectiveness of myPlanKenya. myPlanKenya will be disseminated through formal and informal sectors. This clinical trial portion of the study enrolls women at risk for intimate partner violence (IPV) who are referred to myPlanKenya by disseminators (i.e. "end-users").

This trial aims to evaluate the effectiveness of myPlanKenya referral on resilience, health and safety among a cohort of women referred to myPlanKenya based on disclosure of IPV or assessed to have IPV related risks.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Personalized safety planning tool
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
400 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Dissemination and Implementation of a Web-based Relationship Safety App, myPlanKenya, for Women at Risk for Intimate Partner Violence in Nairobi, Kenya
Actual Study Start Date :
Oct 14, 2022
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Mar 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: myPlan Kenya

myPlan Kenya web-based application

Behavioral: Personalized safety planning tool
The myPlan Kenya app is a web-based safety planning tool that is secure, private, free and personalized to the user. The app includes multiple, evidence-based modules: Strategies (safety strategies tailored to the user's needs and violence experience); Resources (referrals to local health, safety and justice resources and services); About You (questionnaires that help the user assess their relationship safety and tailor their Strategies, including My Relationship, Red Flags, My Safety, My Priorities); Understanding (knowledge sections that share information on relationships and violence, including Healthy Relationships, Harmful Beliefs About Abuse, About Violence).

Outcome Measures

Primary Outcome Measures

  1. Change in decisional conflict [Baseline, 6-month, 12-month]

    12-item pre-intervention and 10-item post-intervention decisional conflict measures (specific to safety), assessed using a 5-point Likert scale (0-4). Items are scored from 0-60 pre-intervention and 0-50 post-intervention, with higher scores indicating higher lower decisional conflict and lower scores indicating higher decisional conflict.

  2. Change in resilience as assessed by Connor-Davidson Resilience Scale [Baseline, 6-month, 12-month]

    10-item Connor-Davidson Resilience Scale, which assesses resilience using a 5-point Likert scale (0-4). Items are scored from 0-40, with higher scores indicating greater resilience and lower scores indicating lower resilience.

  3. Change in safety/IPV experience(s) as assessed by the Conflict Tactics Scale-2 [Baseline, 6-month, 12-month]

    10-item adapted Conflict Tactics Scale-2 (CTS2), which assesses IPV experiences using a 3-point scale on the frequency of these experiences.

  4. Change in help-seeking [Baseline, 6-month, 12-month]

    6-item index on help-seeking, which assesses abuse disclosure and services/information received on a 2-point scale (yes/no), and the helpfulness of these disclosures and services on a 5-point Likert scale. Scale examined for fit and will be handled as individual items as needed.

Secondary Outcome Measures

  1. Change in safety strategies [Baseline, 6-month, 12-month]

    5-item index on safety strategies, which assesses the use of strategies on a 2-point scale (yes/no), and the helpfulness of these strategies on a 5-point Likert scale.

  2. Change in IPV recognition as assessed by the Abusive Behaviors Scale [Baseline, 6-month, 12-month]

    7-item adapted Abusive Behaviors Scale, which assesses IPV recognition using a 5-point Likert scale (0-4). Items are scored from 0-35, with higher scores indicating greater IPV recognition and lower scores indicating lower IPV recognition.

  3. Change in relationship intention [Baseline, 6-month, 12-month]

    Single item which assesses intention for current relationship on a 4-point scale.

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Female

  • Age 16 or older

  • Physical or sexual partner violence or relationship-based fears within the past six months; behaviorally assessed

  • Living in Nairobi, Kenya with no plans to move in the next 12 months

  • Access to a safe smart phone or computer (personal or shared), and comfort using it to access the myPlan Kenya app

  • Literate in English or Swahili languages; confirmed by reading and completing a short passage by filling in several blanks with the appropriate words, selected from a drop-down menu.

Exclusion Criteria:
  • Male

  • Under age 16

  • Have not experienced physical or sexual partner violence or relationship-based fears in past 6 months

  • Lives outside of the study area or plans to move within the next 12 months

  • Does not have access to a safe smart phone or computer, or is uncomfortable using it to access the myPlan Kenya app

  • Illiterate in English or Swahili languages

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ujamaa Africa Nairobi Kenya

Sponsors and Collaborators

  • Johns Hopkins Bloomberg School of Public Health
  • Ujamaa Africa

Investigators

  • Principal Investigator: Michele Decker, Johns Hopkins Bloomberg School of Public Health

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Johns Hopkins Bloomberg School of Public Health
ClinicalTrials.gov Identifier:
NCT05609786
Other Study ID Numbers:
  • IRB00017456
First Posted:
Nov 8, 2022
Last Update Posted:
Nov 8, 2022
Last Verified:
Nov 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Johns Hopkins Bloomberg School of Public Health

Study Results

No Results Posted as of Nov 8, 2022