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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04162730
Other study ID # ATADEK 2019/17
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date January 8, 2020
Est. completion date December 28, 2022

Study information

Verified date February 2022
Source Acibadem University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 150
Est. completion date December 28, 2022
Est. primary completion date December 28, 2022
Accepts healthy volunteers No
Gender All
Age group 40 Years to 75 Years
Eligibility 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.

Study Design


Intervention

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

Locations

Country Name City State
Turkey Özgül Öztürk I?stanbul

Sponsors (1)

Lead Sponsor Collaborator
Acibadem University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Sensitivity Questionnaire The Pain Sensitivity Questionnaire was developed to visualize 17 situations that may feel pain in daily life and to indicate possible pain severity. The patient determines the pain severity level from 0 to 10, with 0 indicates no pain, and 10 indicates the most severe pain. The total score of the Pain Sensitivity Questionnaire and the two subscale scores, PSQ-minor and PSQ-moderate, can be calculated. The PSQ-moderate and PSQ-minor subscales consist of 7 items and the total score is calculated on 14 items. The other 3 items were excluded from the scoring of the scale as they normally indicate painless conditions. Total and subscale scores ranged from 0 to 10, and higher scores indicate increased pain sensitivity. 1-4 week
Secondary Pain Catastrophization Scale It consists of a total of 13 items and is scored between 0-52 points. Higher scores mean higher levels of pain catastrophization. 1-4 week
Secondary Pressure Pain Threshold One day
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