Reliability and Validity of Urdu Version of Ronald Morris Disability Questionnaire in Patients With Low Back Pain

June 20, 2022 updated by: Riphah International University

Urdu Version of The Ronald Morris Disability Questionnaire in Patients With Low Back Pain : Assessing Its Psychometric Properties and Cultural Adaptation.

Purpose of this Research is to convert Ronald Morris Disability Questionnaire into Urdu language and check the accuracy and logic in Pakistani low back pain population. Also check its correlation with Oswestry Disability Index and Visual Analogue Scale.

Study Overview

Status

Recruiting

Conditions

Detailed Description

The Ronald Morris Disability Questionnaire will be translated into Urdu and culturally adapted for people with low back pain. Ronald Morris Disability Questionnaire will be given to 80 people who will be chosen by using a convenient sampling method. Method of sampling based on pre-determined inclusion and exclusion criteria. To examine intra-observer reliability of the final Ronald Morris Disability Questionnaire, two observers will fill out Oswestry Disability Index and Visual Analogue Scale questionnaires on the same day to test inter-observer evaluation. After 30 minutes of the initial treatment, the second application will be applied. The first observer will do the third assessment after seven days. Statistical Package of Social Sciences Version 24 will be used to enter and analyse data. The alpha value of Cronbach's alpha will be examined.

Study Type

Observational

Enrollment (Anticipated)

100

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

    • Punjab
      • Faisalabad, Punjab, Pakistan, 38000
        • Recruiting
        • Ripah International 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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Pakistani population with Chronic Low back pain.

Description

Inclusion Criteria:

  • Average Age of patient 48 years.
  • Patient with chronic low back pain have at least 3 month duration .
  • Patient with mechanical Low Back Pain

Exclusion Criteria:

  • Patient with non - mechanical Low Back Pain
  • Patient have neurological deficits .

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: Ecologic or Community
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Roland-Morris Disability Questionnaire
Time Frame: 1st day
Roland-Morris Disability Questionnaire consist of 24 point according to low back pain population in which patients tell about all Daily Activity . patients scores the questionnaire among 24 points. Roland-Morris Disability Questionnaire is the highest result possible '24'.
1st day
Oswestry Disability Index
Time Frame: 1st day

Oswestry Disability Index is an instrument or scale use for the evaluation of pain . this scale is especially designed for low back pain.

Oswestry Disability Index consist of 10 section or 9 section divide the point out of 50 or 45 . if one section is not score then divided by 45 and get score of patient.after get score multiply with 100 to get percentage. 0 to 21% indicate minimal disability , 21 to 40 indicate moderate disability and 41 to 60 indicate severe disability. 61 to 80 indicate crippled.

1st day
Visual Analogue Scale
Time Frame: 1st day
Visual analog scale is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain".
1st day

Collaborators and Investigators

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

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)

May 30, 2021

Primary Completion (Anticipated)

July 10, 2022

Study Completion (Anticipated)

July 12, 2022

Study Registration Dates

First Submitted

June 20, 2022

First Submitted That Met QC Criteria

June 20, 2022

First Posted (Actual)

June 23, 2022

Study Record Updates

Last Update Posted (Actual)

June 23, 2022

Last Update Submitted That Met QC Criteria

June 20, 2022

Last Verified

June 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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