In Turkish Version Lumbar Spine Surgery Expectation Survey

March 8, 2023 updated by: Ismail Saracoglu, Kutahya Health Sciences University

Turkish Validity and Reliability of Lumbar Spine Surgery Expectation Survey

The aim of this study was to determine the Turkish validity and reliability of Lumbar Spine Surgery Expectations Survey developed by Mancuso.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Although success in lumbar spine surgeries depends on many factors, it has been reported that one of the most important of these factors is patient expectations. In order for patients and health professionals to have the same priorities and meet the same realistic goals, it is necessary to understand what patients expect. Lumbar spine surgery expectations scale was created by Mancuso et al. The aim of this study was to determine the Turkish validity and reliability of Lumbar Spine Surgery Expectations Survey developed by Mancuso.

Study Type

Observational

Enrollment (Actual)

180

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • Turkey
      • Kütahya, Turkey
        • Kutahya Health Sciences 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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients at Kutahya Health Sciences University Hospital will be interviewed in person with two questionnaires.

Description

Inclusion Criteria:

  • speak Turkish
  • arescheduled for lumbar spine surgery by one of two participating spine surgeons

Exclusion Criteria:

  • have cognitive deficits
  • refuse to participate

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lumbar Spine Surgery Expectation Survey
Time Frame: 10 minutes
The Survey has been described in detail previously with respect to validity, reliability, and factor analysis. The Survey addresses pain, function, work status, mental well-being, and anticipated future spine condition.It is prefaced by the question ''How much relief or improvement do you expect in the following areas as a result of the treatment for your spine?'' Response options are ''back to normal or complete improvement'' (4 points), ''not back to normal but a lot of improvement'' (3 points), ''a moderate amount of improvement'' (2 points), ''a little improvement'' (1 point), and ''I do not have this expectation or this expectation does not apply to me'' (0 points).
10 minutes
Quebeck Back Pain Disability Index
Time Frame: 10 minutes
The Quebeck Back Pain Disability Index is a condition-specific measure of disability that was described by Kopec et al. The scale contains 20 daily activities and asks the patient to rate his or her degree of difficulty in performing each activity from 0 ("not difficult at all") to 5 ("unable to do"). The item scores were summed for a total score between 0 and 100, with higher numbers representing greater levels of disability.
10 minutes

Collaborators and Investigators

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

Sponsor

Kutahya Health Sciences University

Investigators

  • Principal Investigator: Metehan YANA, Ph.D., Karabük 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)

February 15, 2021

Primary Completion (Actual)

January 15, 2023

Study Completion (Actual)

February 15, 2023

Study Registration Dates

First Submitted

September 7, 2020

First Submitted That Met QC Criteria

September 7, 2020

First Posted (Actual)

September 14, 2020

Study Record Updates

Last Update Posted (Estimate)

March 9, 2023

Last Update Submitted That Met QC Criteria

March 8, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • KutahyaMSUspinesurgery

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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