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Recruiting NCT06485934

Kinesiophobia Scale for the Upper Extremity

Observational Shoulder Injuries

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Shoulder Injuries. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Development of the Multidimensional Kinesiophobia Scale for the Upper Extremity: A Scale Development Study

Overview

Questionnaires/scales used to evaluate kinesiophobia in the literature are limited and are not specific to the upper extremity in existing scales. For this reason, the primary purpose and subject of the study is to develop a multi-factor kinesiophobia scale specific to shoulder problems. The study is an observational research. Participants will be interviewed twice in total. All primary and secondary outcomes will be assessed at the first meeting. The second come will be performed within 5-7 days after the first assessment. In the second come, only the new kinesiophobia scale that is intended to be developed will be applied.

Primary outcome measures

  • Multidimensional Kinesiophobia Scale (To be developed) [Time frame: Baseline of the study]
  • Multidimensional Kinesiophobia Scale (To be developed) [Time frame: 5-7 days after baseline assessment]
Secondary outcome measures (3)
  • Visual Analog Scale [Time frame: Baseline of the study]
  • Tampa Kinesiophobia Scale [Time frame: Baseline of the study]
  • Demographic Data Form [Time frame: Baseline of the study]

Eligibility criteria

Inclusion criteria

  • Tampa Kinesiophobia Score >37 points
  • Presence of traumatological, orthopedic and rheumatological pathology in the upper extremity
  • Mini-Mental State Examination score >24 points

Exclusion criteria

  • Malignancy,
  • Psychiatric drug use,
  • Use of painkillers during evaluation periods,
  • Those who received physiotherapy before the study (last 6 months),
  • Those whose education level is below secondary school level,

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Turkey (Türkiye) · 2 centers
  • Clinic of İstanbul Hand-Microsurgery Rehabilitation — Istanbul
  • Clinic of İstanbul Hand-Microsurgery Rehabilitation — Istanbul

Identifiers

NCT: NCT06485934 · 2024/74

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗