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Completed

NCT Number: NCT05449314

Reliability and Validity Study of Urdu Version of Modified Barthel Index in Stroke Patients

Aim of the study is to translate and culturally adapt the modified Barthel index into Urdu language and to investigate the reliability and validity of this scale in Urdu speaking Stroke population for performance evaluation. Also check its correlation with Functional independence measure and Katz index of Activities of Daily Living.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Ripah International University

Faisalabad, Punjab Province, 38000, Pakistan

About this study

The English version of the Barthel index will be translated and traditionally adapted as prior endorsement. In Activities of Daily Livings disabled stroke population, Urdu Version of Modified Barthel Index will distributed among sixty participants choose by convenience sampling technique based on pre-distinct inclusion and exclusion standards. To test inter and intra-observer reliability of the final Urdu Version of Modified Barthel Index will be completed on the same day, by two observers, and for the inter-observers evaluation, with an interval of 30 minute between the first and the second submission. Third evaluation will be carried out after 7 days by Observer-1, for intra-observer assessment. Data will be entered and analyzed using Statistical Package of Social Sciences Version 24. Core steadiness will be analyzed with Cronbach alpha value. Test-retest reliability will be evaluated using an intra-class correlation coefficient.The Urdu Version of Modified Barthel Index will be evaluated for content validity, construct validity, criterion validity and responsiveness.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female both genders
  • Adults between the ages of 18 and above
  • Patient suffering from Stroke
  • Ability to provide informed consent

Exclusion criteria

  • Suffering from any cardiovascular pathologies
  • Any disorder of contagious infections
  • Any history of neurological disorders
  • Having any spinal deformity

Treatment and study plan

Primary outcomes

  1. Modified Barthel Index

    Time frame: 1st day

    Modified Barthel Index explained 10 tasks and scores are according to time and assistance needed by the patient between total score from 0 to 20.Lower score describes greater assistance, and larger score tells less assistance required by patient.

  2. Functional Independence Measure

    Time frame: 1st day

    Functional Independence Measure was developed with 18-items that includes, 7-level ordinal scale, with 1 representing dependence and 7 representing independence. This outcome was designed to measure amount and level of help needed to perform Activities of Daily Living by disabled persons.

  3. Katz index of Activities of Daily Living

    Time frame: 1st day

    The Katz Activities of Daily Living Index assesses basic activities of daily living. It does not assess more advanced activities of daily living. Katz developed another scale for instrumental activities of daily living such as heavy housework, shopping, managing finances and telephoning.

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

Cultural Adaptation and Validation of Urdu Version of Modified Barthel Index to Assess the Independence of Pakistani Stroke Patients

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Jul 8, 2022
Registry last updated
Jan 17, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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