Early Detection of Children With Developmental Disabilities in Assiut Governorate

February 15, 2024 updated by: Tayseer Saber Younes, Beni-Suef University

Nurses Training Program for Early Detection of Children With Developmental Disabilities

The study aimed to determine the effectiveness of a designed training program for nurses toward early detection of developmental disabilities among children (0-3 years).

Study Overview

Detailed Description

A group of twenty-one licensed nurses with professional experience ranging from 5 to 11 years participated in the study. The participants completed the measurements to evaluate their current knowledge, practice, and perception pre-, post-, and follow-up of the training program in relation to the early detection of disabilities.

Study Type

Interventional

Enrollment (Actual)

21

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Beni-Suef
      • Banī Suwayf, Beni-Suef, Egypt, 62521
        • Tayseer Saber Abdeldayem

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • The study was conducted in selected health units in Assiut, an Upper Egypt Governorate, in selected villages:

    • far from the main government services,
    • without access to public or subsidized transportation to and from the selected villages, and
    • without the presence of any allied health professionals (physical therapists, occupational therapists, speech and language therapists, psychologists), who do not offer any of these medical services.

The selected nurses should be

  • employed by the village health department in the public sector,
  • locals of the village where the health unit is located,
  • and untrained in the early identification or examination of disabled children.

Exclusion Criteria:

  • other than inclusion criteria

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Nurses group
Nurse training program on early detection of disability. It included four main elements, which are: a booklet defining different disabilities; a list of the guidelines for early detection; a guide for family guidance for families of children with disabilities; and a monitoring and follow-up form for cases of children with disabilities.
It included four main elements, which are: a booklet defining different disabilities, a list of the guidelines for early detection, a guide for family guidance for families of children with disabilities, a monitoring and follow-up form for 8 cases of children with disabilities). The program consisted of twelve training sessions with a total of 48 hours (4 hours per session) and was based on the techniques of lecture, dialogue, working groups, cooperative learning techniques and participatory learning

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Questionnaire of Screening and referral knowledge
Time Frame: 1 month
percentage of nurses' knowledge about screening and referral of all types of developmental disabilities. minimum score is worst, while maximum is the best
1 month
Questionnaire of Disability Perception
Time Frame: 1 month
The degree of needs of children with developmental delays and the importance of early intervention. minimum score is worst, while maximum is the best
1 month
questionnaire about Monitoring Practices
Time Frame: 1 month
Types of nurses' practices about developmental delay monitoring and assessment.minimum score is worst, while maximum is the best
1 month
Follow up
Time Frame: 2 months
The program's long-term learning effect was measured by the previous outcomes. Minimum score is worst, while maximum is the best
2 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Tayseer S Abdeldayem, PhD, Beni-Suef University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Chödrön, G., Pizur-Barnekow, K., Viehweg, S., Puk-Ament, A., & Barger, B. (2019). Childcare providers' attitudes, knowledge, and practice related to developmental monitoring to promote early identification and referral Early Child Development and Care, 1-15. https://doi.org/10.1080/03004430.2019.1626373

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2021

Primary Completion (Actual)

March 15, 2021

Study Completion (Actual)

September 30, 2021

Study Registration Dates

First Submitted

November 26, 2023

First Submitted That Met QC Criteria

February 15, 2024

First Posted (Actual)

February 16, 2024

Study Record Updates

Last Update Posted (Actual)

February 16, 2024

Last Update Submitted That Met QC Criteria

February 15, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

IPD will not be available to any other researchers

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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