Turkish Version of Occupational Balance-Questionnaire (OB-Quest) (OB-QUEST)

March 5, 2021 updated by: ZEYNEP BAHADIR AGCE, Uskudar University

Cross-cultural Adaptation, Reliability and Validity of the Occupational Balance-Questionnaire (OB-Quest) in Turkish

The objective of this study was to translate and culturally adapt the Occupational Balance Questionnaire (OB-Quest) and evaluate the psychometric properties of the translated version by validity and reliability testing.

Study Overview

Detailed Description

This study consists of two parts; in the first part, the translation and cross-cultural adaptation were undertaken, and in the second part, analyses of psychometric properties of OB-Quest Turkish were performed.

Part I: Translation and cross-cultural adaptation

The developers of the original questionnaire were contacted to seek their permission to translate the OB-Quest into Turkish and permission was obtained by the researchers via email. The five-stage translation-back translation method proposed by Beaton et al were used in the cross-cultural adaptation of the questionnaire (Beaton et al., 2000).

The first stage included translation procedures, and two therapists translated the questionnaires' English form into Turkish. In the second stage, two translations were compared to avoid any discrepancy and converted a single text by the research team. Generally, OB-Quest has a simple and understandable sentence structure. Therefore, it did not require any cultural adaptation, simple arrangement was enough to provide clarity. Researchers arranged on the last two items. These items consisting of a single sentence were divided into two as 'example and question', to overcome the complexity of the questions and maintain the integrity of the meaning. After the corrections, researchers had an agreement on the Turkish version of OB-Quest. In the third stage, the back translation of the final text from Turkish to English was made by two native English speakers whose Turkish very well. In the fourth step, the researchers compared the original text with the last English form and produced the final version. The final stage covered the pilot study to get understanding items. After the translation process was completed, a pilot study was conducted with a group of 30 people. Participants approved the final version was appropriate and understandable. The participants in the pilot study did not include in the sample group.

Part II Analysis of the psychometric properties of OB-Quest

Study Type

Observational

Enrollment (Actual)

339

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

    • State
      • Istanbul, State, Turkey, 34662
        • Zeynep Bahadir Agce

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

This study conducted with people who were in the Department of Health Science at the University and their relatives between April 2018 to May 2020. Students, patients, faculty staff or their relatives were invited to the study, those who met the inclusion criteria, and volunteers were asked to complete the forms.

Description

Inclusion Criteria:

  • aged 18-65 years
  • native speakers of Turkish
  • literate of Turkish
  • healthy
  • volunteered to participate in the study

Exclusion Criteria:

  • diagnosed with acute/chronic disease

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
Occupational Balance-Questionnaire (OB-Quest)
Time Frame: 5 minutess.
OB-Quest was developed by Dür et all., as a self-reported outcome instrument to evaluate occupational balance. It was developed based on the experiences of chronic patients and healthy people. The OB-Quest original version internal consistency was shown by Cronbach's alpha as 0.57. It has consisted of ten items and seven components: challenging and relaxing activities; accepted activities; impact of health status on activities; stress, rest and sleep; various activities; and adaptation of activities according to changing living conditions. Each item is scored on a Likert scale ranging from 1 to 3, where 1 indicates a positive score such as 'having a wide variety of activities, and 3 indicates a negative score such as 'not having a wide variety of activities or not showing any variation'. A low score is interpreted as a good occupational balance (Dür et al., 2014).
5 minutess.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Beck Depression Inventory (BDI)
Time Frame: 15 minutes
Beck Depression Inventory was developed by Beck in 1961. It includes 21 items that measure the level of depressive symptoms. Each item contains a four-grade self-assessment that determines depression-specific behavior (Beck, 1961). High scores represent an increase in depressed states. The Turkish scale was adapted by Hisli et al. (Hisli Şahin, 1988).
15 minutes
The 12-item Short Form Survey (SF-12)
Time Frame: 7 minutes
SF-12 was created by simplifying SF-36. It was developed by Ware et al. in 1993 to evaluate quality of life and health outcomes (Ware Jr et al., 1996). SF-12 scores were calculated for each SF-12 physical (SF-12 PCS) and SF-12 mental (SF-12 MCS) component and added to determine the overall score according to the algorithm described by Ware et al. low scores are associated with low quality of life (Ware et al., 1995). It is an easy-to-apply questionnaire with proven reliability and validity in Turkish (Kocyigit et al., 1999).
7 minutes

Collaborators and Investigators

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

Investigators

  • Study Director: ZEYNEP BAHADIR AGCE, PHD, occupational therapy

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.

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)

April 1, 2018

Primary Completion (Actual)

February 10, 2019

Study Completion (Actual)

February 11, 2020

Study Registration Dates

First Submitted

March 3, 2021

First Submitted That Met QC Criteria

March 3, 2021

First Posted (Actual)

March 5, 2021

Study Record Updates

Last Update Posted (Actual)

March 9, 2021

Last Update Submitted That Met QC Criteria

March 5, 2021

Last Verified

March 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • GO 15/735-43

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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