Turkish Adaptation and Validation of the Parent and Youth Forms of the Ohio Youth Scales

September 3, 2026 updated by: Ceyda Sakallı, Istanbul University - Cerrahpasa

Turkish Adaptation and Evaluation of the Validity and Reliability of the Ohio Mental Health Consumer Outcomes System Youth Problem, Functioning, and Satisfaction Scales (Parent and Youth Forms)

This methodological and descriptive study aims to translate and culturally adapt the Parent and Youth Forms of the Ohio Youth Scales into Turkish and to evaluate the validity and reliability of the Turkish versions. Approximately 300 children and adolescents aged 5-18 years and their parents will participate. The Parent Form will be completed by parents of children and adolescents aged 5-18 years, while the Youth Form will be completed by participants aged 12-18 years.

Emotional, behavioral, and psychosocial factors may directly affect participation in daily activities, social functioning, quality of life, and rehabilitation outcomes, particularly among children and adolescents with neurological or chronic conditions. Therefore, the Turkish versions of the scales are expected to support a more comprehensive assessment of psychosocial functioning and service satisfaction in pediatric rehabilitation.

The adaptation process will include forward translation, reconciliation, back-translation, expert review, and pilot testing. Psychometric analyses will examine internal consistency, construct validity, test-retest reliability, agreement, and responsiveness. No medical intervention, invasive procedure, or biological sample collection will be involved.

Study Overview

Detailed Description

Physiotherapy and rehabilitation aim not only to improve physical functions but also to promote participation in daily activities, social adaptation, and quality of life. According to the International Classification of Functioning, Disability and Health framework, health should be evaluated by considering body structures and functions, activity, participation, and environmental factors. Emotional status, behavioral characteristics, and psychosocial functioning may directly influence rehabilitation, particularly among children and adolescents with neurological or chronic conditions.

The Ohio Youth Scales provide multidimensional assessments of problems, functioning, and satisfaction through Parent and Youth Forms. The Turkish adaptation of these instruments may facilitate the assessment of psychosocial status and social participation among children and adolescents receiving rehabilitation services. The scales may also support physiotherapists within multidisciplinary assessment, contribute to the development of rehabilitation goals that reflect psychosocial needs, and provide valid and reliable instruments for future clinical and academic research.

This methodological and descriptive observational study aims to translate and culturally adapt the Parent and Youth Forms of the Ohio Youth Scales into Turkish and evaluate their psychometric properties. Approximately 300 children and adolescents aged 5-18 years and their parents will voluntarily participate. The Parent Form will be administered to parents of children and adolescents aged 5-18 years, while the Youth Form will be administered to participants aged 12-18 years.

The adaptation process will be conducted in accordance with international guidelines for the cross-cultural adaptation of measurement instruments. First, the original forms will be independently translated from English into Turkish by at least two researchers who are proficient in both languages and knowledgeable in the relevant field. The translations will be compared and reconciled to produce a common Turkish version.

The reconciled Turkish version will then be independently translated back into English by translators who are native English speakers or have advanced proficiency in English and who have not reviewed the original forms. The back-translated versions will be compared with the original instruments to evaluate conceptual equivalence and consistency of meaning.

Expert opinions will subsequently be obtained to evaluate linguistic appropriateness, cultural relevance, and content validity. Necessary revisions will be made based on the expert evaluations, resulting in a preliminary Turkish version. This preliminary version will be pilot-tested with a limited number of individuals from the target population. Participants' understanding of the items will be evaluated, and unclear expressions will be revised before the final Turkish forms are produced.

Data will be collected face-to-face or in another appropriate setting. Completion of the questionnaires is expected to take approximately 15-20 minutes. A second administration will be conducted after a two-week interval to assess test-retest reliability.

The Strengths and Difficulties Questionnaire will be used to assess emotional and behavioral difficulties, and the Psychological Well-Being Scale will be used to assess psychological well-being as part of the validity evaluation. Relationships between the Parent and Youth Forms will also be examined.

Descriptive statistics will include frequencies and percentages for categorical variables and means, medians, standard deviations, and ranges for continuous variables. Internal consistency will be evaluated using Cronbach's alpha coefficients. Construct validity will be examined using confirmatory factor analysis. Test-retest reliability will be evaluated using intraclass correlation coefficients based on a two-way mixed-effects model. Measurement error and agreement will be assessed using the standard error of measurement and minimal detectable change. Responsiveness may be evaluated using Global Rating of Change scores or other appropriate validated measures. Statistical significance will be set at p<0.05.

No medical intervention or invasive procedure will be performed. No biological samples will be collected, and no biochemical, hematological, genetic, or other laboratory examinations will be conducted.

Study Type

Observational

Enrollment (Estimated)

300

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

    • Istanbul
      • Istanbul, Istanbul, Turkey (Türkiye), 34500
        • Istanbul University - Cerrahpasa, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
        • Contact:

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

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The study population will consist of approximately 300 children and adolescents aged 5-18 years and their parents. Parents of participants aged 5-18 years will complete the Parent Form of the Turkish Ohio Youth Scales. Participants aged 12-18 years will additionally complete the Youth Form. Participants will not be required to have a specific medical or psychiatric diagnosis. A subgroup that voluntarily agrees to participate in the second assessment will complete the scales again after two weeks for the evaluation of test-retest reliability.

Description

Inclusion Criteria:

Being aged 5-18 years for participation through the Parent Form Being aged 12-18 years for participation through the Youth Form Voluntary participation of the child or adolescent and their parent Provision of written informed consent by the parent Provision of written assent by participants aged 12 years or older Having sufficient Turkish reading and comprehension skills to understand the items For the test-retest assessment, having completed the initial assessment and voluntarily agreeing to complete the second assessment

Exclusion Criteria:

Being outside the specified age range Absence of written informed consent from the parent Absence of written assent from participants aged 12 years or older Insufficient Turkish reading or comprehension skills to understand the items Substantially incomplete or incorrectly completed questionnaires Failure to complete the second assessment, only for inclusion in the test-retest analyses

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

Cohorts and Interventions

Group / Cohort
Children Aged 5-11 Years
Parents of children aged 5-11 years will complete the Parent Form of the Turkish Ohio Youth Scales.
Adolescents Aged 12-18 Years
Parents of adolescents aged 12-18 Years will complete the Parent Form, and adolescents will complete the Youth Form of the Turkish Ohio Youth Scales.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Psychometric Properties of the Turkish Ohio Youth Scales Parent Form
Time Frame: At the initial assessment and two weeks after the initial assessment
The Turkish Parent Form of the Ohio Youth Scales will be completed by parents of children and adolescents aged 5-18 years. The form assesses the child's or adolescent's problems, functioning, and satisfaction with services. Its psychometric properties will be evaluated through internal consistency, construct validity, test-retest reliability, measurement error, and agreement analyses. Internal consistency will be examined using Cronbach's alpha, and test-retest reliability will be assessed using intraclass correlation coefficients.
At the initial assessment and two weeks after the initial assessment
Psychometric Properties of the Turkish Ohio Youth Scales Youth Form
Time Frame: At the initial assessment and two weeks after the initial assessment
The Turkish Youth Form of the Ohio Youth Scales will be completed by adolescents aged 12-18 years. The form assesses problems, functioning, and satisfaction with services from the adolescent's perspective. Its psychometric properties will be evaluated through internal consistency, construct validity, test-retest reliability, measurement error, and agreement analyses. Internal consistency will be examined using Cronbach's alpha, and test-retest reliability will be assessed using intraclass correlation coefficients.
At the initial assessment and two weeks after the initial assessment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Convergent Validity With the Strengths and Difficulties Questionnaire
Time Frame: At the initial assessment
The Strengths and Difficulties Questionnaire will be used to evaluate the convergent validity of the Turkish Ohio Youth Scales. The validated Turkish Parent Form will be completed by parents of eligible participants, and the validated Turkish self-report form will be completed by eligible adolescents. Associations between the Strengths and Difficulties Questionnaire scores and the corresponding problem and functioning scores of the Turkish Ohio Youth Scales will be examined.
At the initial assessment
Convergent Validity With the Psychological Well-Being Scale
Time Frame: At the initial assessment
The validated Turkish version of the Psychological Well-Being Scale will be used to support the construct validity of the Turkish Ohio Youth Scales. Associations between psychological well-being scores and the corresponding scores obtained from the Turkish Ohio Youth Scales will be examined.
At the initial assessment

Collaborators and Investigators

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

Investigators

  • Study Chair: Sezen Karaborklu Argut, PhD, Istanbul University - Cerrahpasa, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation

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)

September 15, 2026

Primary Completion (Estimated)

August 15, 2027

Study Completion (Estimated)

September 15, 2027

Study Registration Dates

First Submitted

September 3, 2026

First Submitted That Met QC Criteria

September 3, 2026

First Posted (Actual)

September 8, 2026

Study Record Updates

Last Update Posted (Actual)

September 8, 2026

Last Update Submitted That Met QC Criteria

September 3, 2026

Last Verified

September 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared due to participant confidentiality and ethical considerations, particularly given that the study involves children and adolescents.

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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