Validity, Reliability and Responsiveness of Pain Sensitization Questionnaire

NCT ID: NCT04162730

Last Updated: 2022-02-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-01-08

Study Completion Date

2022-12-28

Brief Summary

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The aim of this study was to translate the Pain Sensitivity Questionnaire, which was developed to determine the level of pain sensitivity of individuals, to Turkish and to evaluate the validity and reliability of the Turkish version of the scale on knee osteoarthritis patients, and as well as to perform cultural adaptation. Pain sensitivity assessment is used to predict treatment or surgical outcomes of individuals. IPain Sensitivity Questionnaire is a frequently used scale that correlates with experimental pain tests and is used in studies conducted in different patient groups. We believe that adding this scale to our language will contribute to other studies in this field.

Detailed Description

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Conditions

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Pain Syndrome Pain, Chronic Knee Osteoarthritis

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Interventions

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Pressure pain threshold and behavioural data

Pressure pain threshold level of the knee region will be collected and behavioural data will be measured

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Not having oral or written communication problems in Turkish,
* Diagnosis of knee osteoarthritis after clinical examination and radiological imaging,
* Being 40 years or older,
* To have neurological competence and cognitive level to answer scale questions.

Exclusion Criteria

* To have fibromyalgia syndrome or neurological disease that may affect pain sensitivity levels of individuals,
* To have undergone surgery involving the knee in the last 1 year,
* The presence of peripheral neuropathy and neuropathy is therefore to be taking medication.
Minimum Eligible Age

40 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Acibadem University

OTHER

Sponsor Role lead

Responsible Party

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Özgül Öztürk

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Özgül Öztürk

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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ATADEK 2019/17

Identifier Type: -

Identifier Source: org_study_id

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