MedTrace Logo

Mobile Applications Development for Prevention of Sexual Abuse

NCT05737134 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 301

Last updated 2023-03-14

No results posted yet for this study

Summary

This interventional study aims to examine the effect of implementing new tools for preventing child sexual abuse (CSA) using a designed digital application for parents/teachers.

The main question of this study is How is the effect of the Mobile Application for Prevention of Sexual Violence in Elementary School-aged Children by Involving the Roles of Parents and School Teachers in West Java on knowledge, attitudes, communication practices, and self-awareness of parents and teachers in West Java.

Two randomized groups of parents will receive or not receive a package of information using a mobile application called MA\_PESAN.

The MA\_PESAN application is precise and can increase teachers' and parents' knowledge, attitudes, communication practices, and self-awareness about preventing CSA. This application is recommended to be applied in all elementary-level schools.

Conditions

  • Child Sexual Abuse
  • Mobile Application

Interventions

OTHER

MA_PESAN MOBILE APPLICATION

The intervention group was given a mobile application consisting of video, and educational material that information was provided regarding the prevention of child sexual abuse.

Sponsors & Collaborators

  • Universitas Padjadjaran

    lead OTHER

Principal Investigators

  • Henny S Mediani, MNg., PhD · Universitas Padjadjaran

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-04-01
Primary Completion
2022-12-15
Completion
2022-12-15

Countries

  • Indonesia

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05737134 on ClinicalTrials.gov