Turkish Validity and Reliability Study of PRevention of Toxic Chemicals in the Environment for Children Tool

March 16, 2026 updated by: Rukiye Duman, Istanbul University - Cerrahpasa

Turkish Validity and Reliability Study of PRevention of Toxic Chemicals in the Environment for Children Tool (PRoTECT)

The aim of this study is to conduct a Turkish validity and reliability study of the "Prevention of Toxic Chemicals in the Environment for Children Tool," developed to examine the knowledge and attitudes of parents and prospective parents regarding the effects of toxic chemicals in the environment on children's development.

Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

204

Contacts and Locations

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

Study Contact

Study Locations

  • Turkey (Türkiye)
    • AVCILAR
      • Istanbul, AVCILAR, Turkey (Türkiye), 34310
        • Recruiting
        • Rukiye Duman

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Probability Sample

Study Population

The research population will consist of parents or prospective parents. Literature indicates that in methodological research, the sample size required to test the validity and reliability of measurement instruments should be 10-15 times the number of items in the scale (Esin, 2024). Accordingly, in this research, the minimum required sample size was planned as 12 times the number of items in the measurement instrument (17 x 12 = 204), based on this rule.

Description

Inclusion Criteria:

Adult parents and prospective parents

Exclusion Criteria:

Illiterate

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
"Prevention of Toxic Chemicals in the Environment for Children Tool" Turkish validity and reliability
Time Frame: 1 months
"To conduct the Turkish validity and reliability study of the 'Prevention of Toxic Chemicals in the Environment for Children Tool'."
1 months
The Relationship Between Knowledge and Attitudes Towards Prevention of Toxic Chemicals in the Environment for Children and Environmental Literacy
Time Frame: 1 months
The study also examines the relationship between parents' and prospective parents' knowledge and attitudes towards toxic chemicals in the environment that negatively affect child development and their environmental literacy.
1 months

Collaborators and Investigators

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

Sponsor

Istanbul University - Cerrahpasa

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 (Estimated)

March 16, 2026

Primary Completion (Estimated)

April 3, 2026

Study Completion (Estimated)

May 4, 2026

Study Registration Dates

First Submitted

March 16, 2026

First Submitted That Met QC Criteria

March 16, 2026

First Posted (Actual)

March 19, 2026

Study Record Updates

Last Update Posted (Actual)

March 19, 2026

Last Update Submitted That Met QC Criteria

March 16, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • IstanbulUC-EBE-RD-03

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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