In Turkish Version "Health Care Providers and Impairment Relationship Scale (HC-PAIRS)"

March 3, 2021 updated by: Ismail Saracoglu, Kutahya Health Sciences University

Turkish Validity and Reliability of "Health Care Providers and Impairment Relationship Scale (HC-PAIRS)"

The aim of this study was to determine the Turkish validity and reliability of ''Health Care Providers and Impairment Relationship Scale HC (HC-PAIRS)'' developed by Dr Rainville.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Low back pain is one of the reasons for applying to health institutions. Low back pain, which seriously affects patients' lives and leads to major financial losses, causes serious deficiencies in both developing and developed countries. Health professionals' perception of pain, factors associated with pain and fear avoidance attitudes of patients affect the success of treatment. The aim of this study is to determine the Turkish version, validity and reliability of ''Health Care Providers and Impairment Relationship Scale (HC-PAIRS)''. 165 physiotherapist working with chronic low back pain were included in the study. In order to determine the reliability of the scale, the intraclass correlation coefficient (ICC) will be used to determine the level of the relationship between the results of the first and second measurements. Cronbach's alpha coefficient will be used for homogeneity of the questions in the scale. For concurrent validity, correlation coefficient will be used to determine the agreement between the previously validated scales and the Turkish version of HC PAIRS.

Study Type

Observational

Enrollment (Actual)

165

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

  • Turkey
      • Kütahya, Turkey
        • Kütahya Health Science University

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

19 years to 63 years (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

The study will be carried out by physiotherapists working in the KSBU Evliya Celebi Hospital or accessible via internet.

Description

Inclusion Criteria:

  • Graduate with a bachelor's degree in physiotherapy and rehabilitation
  • To have worked in patients with chronic low back pain

Exclusion Criteria:

  • Not having experience in the clinic about low back pain

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

  • Observational Models: Other
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Health Care Providers' Pain and Impairment Relationship Scale
Time Frame: 10 minute
The Health Care Providers' Pain and Impairment Relationship Scale (HC-PAIRS) is a questionnaire for assessing the attitudes and beliefs of health care providers about functional expectations for CLBP patients.17 It consists of 15 statements rated on a 6-point Likert scale ranging from "totally disagree" to "totally agree."
10 minute
Turkish version of Tampa Scale for Kinesiophobia
Time Frame: 10 minute
TSK was used for the assessment of kinesiophobia. The items are rated on a 4-point Likert-type scale (1=definitely disagree, 4=completely agree) and the total score is between 17 and 68 points. Higher total score indicates higher level of kinesiophobia.
10 minute

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain Attitudes and Beliefs Scale for Physiotherapists (PABS-PT)
Time Frame: 10 minute.
This tool was developed to distinguish between biomedical and biopsychosocial orientations toward the treatment of low back pain in physiotherapists. The scale uses a 6-point Likert-type scale (1=definitely disagree, 6=definitely agree). Treatment orientation is measured on the biomedical (factor 1) and biopsychosocial (factor 2) subscales. Subscale scores are calculated by simply adding the scores corresponding to the selected response for each item. The subscale with the highest score indicates the respondent's dominant treatment orientation
10 minute.

Collaborators and Investigators

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

Sponsor

Kutahya Health Sciences University

Investigators

  • Study Director: Cihan C AKSOY, PhD, Kütahya Health Science University
  • Principal Investigator: Ismail Saracoglu, Phd, Kütahya Health Science University
  • Principal Investigator: Lütfiye AKKURT, MSc, Kütahya Health Science University

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)

September 30, 2019

Primary Completion (Actual)

February 15, 2020

Study Completion (Actual)

August 30, 2020

Study Registration Dates

First Submitted

August 2, 2019

First Submitted That Met QC Criteria

August 2, 2019

First Posted (Actual)

August 6, 2019

Study Record Updates

Last Update Posted (Actual)

March 4, 2021

Last Update Submitted That Met QC Criteria

March 3, 2021

Last Verified

March 1, 2021

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • KutahyaMSUt

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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