Urdu Version of Northwick Park Neck Pain Questionnaire: Reliability and Validity Study

January 28, 2024 updated by: Riphah International University

Is Urdu Version of Northwick Park Neck Pain Questionnaire a Culturally Adaptable and Valid Tool to Assess the Neck Pain in Pakistani Population?

  • To adapt culturally Neck Pain Questionnaire in Urdu language.
  • To check the reliability of Urdu version of Neck Pain Questionnaire
  • To validate Neck Pain Questionnaire by Neck Disability Index and Visual Analogue Scale and Numeric Pain Rating Scale.

Study Overview

Status

Completed

Conditions

Detailed Description

The original English version of Northwick Park Neck Pain Questionnaire will be translated and culturally adapted as per previous recommendation. In patients with neck pain, Urdu Version of Northwick Park Neck Pain Questionnaire will be distributed among 70 participants choose a convenience sampling technique based on pre-defined inclusion and exclusion criteria. To test reliability of inter/intra observer of ultimate final Urdu Version of Northwick Park Neck Pain Questionnaire will be filled from patients on the equivalent day, by 2 different bystanders, and for inter observer valuation, with an interval of 30 minutes between the first and second application. Third assessment will be carried out after 7 days of the Observer -1, for intra-observer assessment. Data will be entered and analyzed Cronbach alpha value. Test-retest reliability will be assessed using an intraclass correlation coefficient. Urdu Version of Northwick Park Neck Pain Questionnaire will be evaluated for content validity, construct validity, criterion validity and responsiveness.

Study Type

Observational

Enrollment (Actual)

70

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
        • 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

18 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

People suffering from chronic neck pain with a working routine of more than 3 to 4 both in sitting and standing position.

Description

Inclusion Criteria:

  1. Both Male and Female
  2. Minimum age is 18 years
  3. Maximum age up to 60 years
  4. People with Chronic neck pain
  5. Duration of pain more then 3 months
  6. No history of neck therapy
  7. Not had any neck therapy

Exclusion Criteria:

  1. People with medical history regarding skeleton issues
  2. People with traumas
  3. Having Neck surgery
  4. People with neurological deficits ( like malignancies or inflammatory arthritis)
  5. People went for therapy were also excluded.
  6. People with age more than 60 and less than 18 were excluded..

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
Neck Disability Index
Time Frame: 1st day
Neck Disability Index includes ten questions that assess pain intensity, personal care, lifting, reading, headaches, attention, work, driving, sleeping, and recreational activities. Every question is graded on a scale of 0 to 5 (no disability to total disability).
1st day
Visual Analogue Scale
Time Frame: 1st day
The Visual Analogue Scale was created to represent the concept of a fundamental continuity. A Visual Analogue Scale is typically a straight stripe measuring 100 mm long, with word descriptions for each end. The patient draws a line through the spot on the line which they believe best describes their present state. The Visual Analogue Scale score is calculated by calculating in millimeters as from the line's left side to the point marked by that of the patient. It usually ranges from "0" indicating "no pain" to the "10" indicating "worst pain".
1st day
Northwick Park Neck Pain Questionnaire
Time Frame: 1st day
Each parameter of Northwick Park Neck Pain Questionnaire has divided into 5 answers with total of 10 parameters. Each parameter is divided in five answer possibilities with points from 0 till 4. 0 is significant for no pain and 4 is significant for worst pain.
1st day
Numeric Pain Rating Scale
Time Frame: 1st day
Numeric Pain Rating Scale has a line value ranging from 1 to 10, 1 being the no pain label and 10 being the worst pain.
1st day

Collaborators and Investigators

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

Investigators

  • Study Chair: Muhammad Kashif, Riphah International 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)

May 30, 2021

Primary Completion (Actual)

December 20, 2022

Study Completion (Actual)

December 20, 2022

Study Registration Dates

First Submitted

June 27, 2022

First Submitted That Met QC Criteria

June 27, 2022

First Posted (Actual)

June 30, 2022

Study Record Updates

Last Update Posted (Actual)

January 30, 2024

Last Update Submitted That Met QC Criteria

January 28, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC-FSD-00269

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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