Palestinian ParentText for Crisis: A Parenting Chabot in War
ParentText for Crisis: A Randomised Controlled Trial of Chatbot-Delivered Mental Health and Parenting Content For Palestinian Caregivers in Jordan
2 other identifiers
interventional
198
1 country
1
Brief Summary
The primary aim of this research is to evaluate if ParentText for Crisis helps improve the following outcomes among Palestinian caregivers living in Jordan: a.) Improving caregiver mental health; b.) Improving positive parenting practices; c.) Reducing violence against children
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
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
February 11, 2026
CompletedFirst Submitted
Initial submission to the registry
March 9, 2026
CompletedFirst Posted
Study publicly available on registry
March 27, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 26, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 26, 2026
CompletedMay 4, 2026
February 1, 2026
2 months
March 9, 2026
April 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Caregiver Depression
Caregiver depression is measured via Patient Health Questionnaire - 2 (PHQ-2). PHQ-2 includes two questions on depression, with likert scale answer options ranging 0-3. Higher scores indicate higher levels of depression.
Intervention arm: Outcome is collected at trial baseline and +30 days post-baseline. Control arm: Outcome is collected at +30 days post-baseline.
Playful Parenting
Parenting Practices are measured via a positive parenting item adapted from Alabama Parenting Questionnaire, measuring frequency of playing with children in the past week. Survey responses are reported in days of occurrence within the past week (0-7), with higher scores indicating higher level of playful parenting.
Intervention arm: Outcome is collected at trial baseline and +30 days post-baseline. Control arm: Outcome is collected at +30 days post-baseline.
Secondary Outcomes (3)
Caregiver Hopefulness
Intervention arm: Outcome is collected at trial baseline and +30 days post-baseline. Control arm: Outcome is collected at +30 days post-baseline.
Parenting Practices
Intervention arm: Outcome is collected at trial baseline and +30 days post-baseline. Control arm: Outcome is collected at +30 days post-baseline.
Violence Against Children
Intervention arm: Outcome is collected at trial baseline and +30 days post-baseline. Control arm: Outcome is collected at +30 days post-baseline.
Study Arms (2)
ParentText for Crisis
EXPERIMENTALA rule-based chatbot to provide tips to strengthen parental mental health, improve parenting practices, and help parents support children in crisis settings
Comparison Group
NO INTERVENTIONWait-List Control Group
Interventions
A rule-based chatbot to provide tips to strengthen parental mental health, improve parenting practices, and help parents support children in crisis settings
Eligibility Criteria
You may qualify if:
- Adult (aged \>=18)
- Parent or caregiver of \>=1 child
- Living in Jerash Camp, Jerash, Jordan (a refugee camp for Palestinians from Gaza)
- Have access to a phone with WhatsApp
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Oxfordlead
- Sanadakcollaborator
Study Sites (1)
Jerash Camp
Jerash, Jordan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- Analysts are blinded during all analyses.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 9, 2026
First Posted
March 27, 2026
Study Start
February 11, 2026
Primary Completion
April 26, 2026
Study Completion
April 26, 2026
Last Updated
May 4, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, ANALYTIC CODE
- Time Frame
- A brief protocol is available on Open Science Framework: https://osf.io/q5s4k/overview. The Statistical Analysis Plan will be registered on Open Science Framework prior to any analysis (estimated date: end of March 2026). Consent forms and analytic code will be posted on OSF at time of manuscript submission.
- Access Criteria
- Requests for data access can be made to Sydney Tucker at sydney.tucker@spi.ox.ac.uk. Anonymous data will be made publicly available after RCT results are published.
IPD, including all outcome and demographic outcomes, will be shared.