Translation and Validation of Pelvic Girdle Questionnaire in Urdu Language

February 20, 2023 updated by: Riphah International University
Urdu version of pelvic girdle questionnaire was drafted, tested for its reliability and validity on patients with pelvic girdle pain. Urdu version was linguistically acceptable and accurate for pregnant and post partum females with pelvic girdle pain. The result seems comparable to all the other versions and especially with original Norwegian version. This instrument is understandable and easy to find disability during pregnancy and post partum duration. It showed a good content, construct and convergent validity also present high internal consistency and test retest reliability.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The Pelvic Girdle Questionnaire is the only specific instrument designed to evaluate pain and activity limitations in pregnant or postpartum women with pelvic girdle pain. This study aimed to translate the Pelvic girdle questionnaire in Urdu language for Pakistani female patients and to verify the validation of the psychometric items of the Pelvic girdle questionnaire in population of Pakistan. The purpose of this study was to translate the Pelvic Girdle Questionnaire into Urdu and find out cross-culture validity and reliability of Urdu Pelvic girdle questionnaire among pregnant and postpartum females. A cultural adaptation and translation study was performing according to international guidelines. Study was conducted at different hospital settings. Pre test was conducted among 16 females during pregnancy & post-partum.

Key words: Disability Evaluation, Female, Urdu, Pelvic Girdle Pain and physiopathology, Pregnancy, Surveys and Questionnaires, Translation.

Study Type

Observational

Enrollment (Actual)

125

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
      • Gujrat, Punjab, Pakistan, 50931
        • Faiza Kalsoom

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 50 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Female pregnant and post partum with pelvic girdle pain

Description

Inclusion Criteria:

  • Age 18-50 years
  • Only Females
  • Able to read Urdu Language
  • Pregnant women (gestational week 30-38)
  • Postpartum women (given birth less than one year earlier)

Exclusion Criteria:

  • Any neurological diseases (reflex changes & loss of sensation)
  • Unstable medical conditions leading to fatigue
  • Those that have prolapse or severe urinary disease
  • Previous surgery on pelvis, lower limb or spine
  • Cannot Understand Urdu
  • Difficulty in understanding the Pelvic girdle questionnaire

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
Content validity
Time Frame: "through study completion, an average of 1 year"
Content validity score measured by content validity index. Assessment of 25 items by Clinician and native speaker experts rate all the items and all the value are above 0.70.Lower value was 0.92 and the highest value is 1 which is maximum value. Maximum score is given to 4, 5, 6,10,11,12,17,18,22 and 24 by experts (medical specialist and native speakers).
"through study completion, an average of 1 year"

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Internal consistency:
Time Frame: "upto two weeks"
Cronbach's alpha was used for reliability. The reliability and internal consistency of PGQ for PGP patients Cronbach's alpha in week one and week two is 0.977 and 0.976 respectively. The value of α for activity subscale (1-20) is 0.986 and symptom subscale (21- 25) is 0.970.
"upto two weeks"

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Convergent validity
Time Frame: "through study completion, an average of 1 year"
The value of Pearson correlation coefficient for Pelvic girdle questionnaire with Ostwestry disability index is 0.840 and NRS is 0.772.For the calculation of construct validity of PGQ we used Pearson's correlation coefficient with 5% significance. The correlation between week 1 and week 2 for each item of PGQ scale was ranging from 0.871-0.990. . We compared PGQ with ODI scale and Numeric rating pain scale. The construct validity of PGQ was measured by confidence interval 95% and level of significance at 5%.
"through study completion, an average of 1 year"
Test Retest reliability:
Time Frame: "through study completion, an average of 1 year"
The tool reliability analyzes by ICC. The value of Intra class correlation for PGQ is 0.979 with 95 % of confidence interval.
"through study completion, an average of 1 year"

Collaborators and Investigators

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

Investigators

  • Principal Investigator: sumera abdul hameed, Ms, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

January 2, 2021

Primary Completion (Actual)

January 31, 2022

Study Completion (Actual)

January 31, 2022

Study Registration Dates

First Submitted

October 21, 2022

First Submitted That Met QC Criteria

February 20, 2023

First Posted (Actual)

March 2, 2023

Study Record Updates

Last Update Posted (Actual)

March 2, 2023

Last Update Submitted That Met QC Criteria

February 20, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Faiza Kalsoom

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.

Clinical Trials on Pelvic Girdle Pain

Clinical Trials on Straight leg raise

Subscribe