NCT07494786

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

77
On Track

Trial Health Score

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

Enrollment
480

participants targeted

Target at P75+ for not_applicable

Timeline
5mo left

Started Feb 2026

Geographic Reach
1 country

1 active site

Status
recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress62%
Feb 2026Feb 2027

Study Start

First participant enrolled

February 11, 2026

Completed
26 days until next milestone

First Submitted

Initial submission to the registry

March 9, 2026

Completed
18 days until next milestone

First Posted

Study publicly available on registry

March 27, 2026

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2027

Last Updated

August 27, 2026

Status Verified

February 1, 2026

Enrollment Period

10 months

First QC Date

March 9, 2026

Last Update Submit

August 24, 2026

Conditions

Keywords

WarChatbotRefugeeDisplacementMental HealthParentingViolence Against Children

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

EXPERIMENTAL

A rule-based chatbot to provide tips to strengthen parental mental health, improve parenting practices, and help parents support children in crisis settings

Behavioral: ParentText for Crisis

Comparison Group

NO INTERVENTION

Wait-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

ParentText for Crisis

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Jerash Camp

Jerash, Jordan

RECRUITING

MeSH Terms

Conditions

Psychological Well-Being

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior

Central Study Contacts

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 (Estimated)

December 15, 2026

Study Completion (Estimated)

February 28, 2027

Last Updated

August 27, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will share

IPD, including all outcome and demographic outcomes, will be shared.

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.

Locations