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Completed

NCT Number: NCT04373681

Validity and Reliability of the Turkish Version of WOOS

Various clinical scales are available to investigate shoulder diseases. Some of them, culturally adapted to the Turkish population. However, none of them are specific for osteoarthritis of the shoulder. Thus, this study aimed to translate the WOOS index into Turkish and investigate its psychometric properties in the Turkish population.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Ankara Training and Research Hospital, Department of Orthopaedics & Traumatology, Ankara, Turkey (Türkiye)

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About this study

Purpose; The aim of this study is to adapt the Western Ontario Osteoarthritis of the Shoulder Index (WOOS) specific to shoulder osteoarthritis, to Turkish and evaluate its validity and reliability.

Methods; WOOS index was translated and culturally adapted to Turkish, systematically. It was applied to 68 patients with osteoarthritis of the shoulder treated conservatively. The reliability of the scale was checked through internal consistency and test-retest methods. Internal consistency was analyzed with Cronbach's alpha value. Test-retest reliability was assessed using an intraclass correlation coefficient with 25 patients. The Western Ontario Rotator Cuff (WORC), The Shoulder Pain and Disability Index (SPADI), and The Society of American Shoulder and Elbow Surgeons Standardized Shoulder Assessment (ASES) score were used to conduct concurrent validity.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Presence of the shoulder osteoarthritis, to be a native Turkish speaker

Exclusion criteria

  • Illiteracy, cognitive impairment, presence of shoulder circumference fractures

Treatment and study plan

patient-administered questionnaires

Other

patient-administered questionnaires

Primary outcomes

  1. Western Ontario Osteoarthritis of the Shoulder Index, patients get a minimum of 0 points (best condition) and a maximum of 1900 points (worst condition) on this scale.

    Time frame: 1st day

    patient administered, spesific to osteoarthritis of shoulder, multisectional questionnaire

  2. Western Ontario Osteoarthritis of the Shoulder Index, patients get a minimum of 0 points (best condition) and a maximum of 1900 points (worst condition) on this scale.

    Time frame: 2 days later

    patient administered, spesific to osteoarthritis of shoulder, multisectional questionnaire

  3. The Western Ontario Rotator Cuff Index, patients get a minimum of 0 points (best condition) and a maximum of 2100 points (worst condition) on this scale.

    Time frame: 1st day

    patient administered, spesific to rotator cuff disease, multisectional questionnaire

  4. The Shoulder Pain and Disability Index, patients get a minimum of 0 points (best condition) and a maximum of 100 points (worst condition) on this scale.

    Time frame: 1st day

    patient administered, spesific to upper limp, two sectional questionnaire

  5. The Society of American Shoulder and Elbow Surgeons Standardized Shoulder Assessment, patients get a minimum of 0 points (worst condition) and a maximum of 100 points (best condition) on this scale.

    Time frame: 1st day

    patient administered, spesific to upper limp, two sectional questionnaire

Sponsors and collaborators

Lead sponsor

Gazi University

Other

Registry information

Official study title

Validity and Reliability of the Turkish Version of Western Ontario Osteoarthritis of the Shoulder Index

Important dates

Study start
2017
Primary completion
2020
Study completion
2020
First posted
May 4, 2020
Registry last updated
Apr 19, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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