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Clinical Trials/CTRI/2024/12/078591
CTRI/2024/12/078591
Not yet recruiting
Not Applicable

Development and Validation of a Patient Reported Outcome Measure in Indian patients with known cardiac dysfunctions

Prajakta Sahasrabudhe1 site in 1 country300 target enrollmentStarted: January 31, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Prajakta Sahasrabudhe
Enrollment
300
Locations
1
Primary Endpoint
Newly developed outcome tool to assess Quality of Life

Overview

Brief Summary

Although there is a wide choice of generic and disease specific patient reported outcome measures (PROM) available for patients diagnosed with cardiac pathologies, most of those are specific to diagnoses than for impairments perceived by the patients and fail to assess multiple aspects of impairments, activities and participations and contextual factors and domains of health-related quality of life comprehensively. Concept of HRQOL varies with respect to attitude, cultural practices and idea of societal participation; hence PROMs used to assess HRQOL might not be generalizable outside the boundaries of these culture specific factors.  None of the available tools for cardiac diseases were developed considering Indian cultural practices and beliefs at its core. All these factors necessitate need of a new and more comprehensive PROM for use in Indian adult patients who have either conservatively or surgically treated cardiac disease.  In the present proposal, we present the idea of development and validation of a patient reported tool to assess HRQOL in these patients.

In the development phase of the study, patients having known cardiac dysfunctions and stable disease will be assessed qualitatively and quantitatively to understand their lifestyle, severity and impact of disease related impairments, limitations in activities and participation and factors affecting these. On the basis of above assessment, a closed ended questionnaire will be generated in English, Hindi and Marathi with multiple choice options based on Likert scale by choosing relevant clinical items. In the validation phase, the questionnaire developed will be validated for its outline and contents by experts in the field. The final version of the questionnaire will be presented to a cohort of patients having diagnosed cardiac dysfunctions and construct validity, reliability and responsiveness of the tool will be established.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
35.00 Year(s) to 70.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Having a diagnosis of a myocardial infarction or valvular heart disease or compensated heart failure or cardiomyopathy for more than a month ago Have undergone percutaneous transluminal coronary angioplasty or coronary artery bypass grafting or valvular repair or replacement or intracardiac repair for congenital heart disease.

Exclusion Criteria

  • Any known illness affecting any body structure or function other than CVS system acute/exacerbated/unstable heart condition, frail or bedridden patient.

Outcomes

Primary Outcomes

Newly developed outcome tool to assess Quality of Life

Time Frame: Baseline

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Prajakta Sahasrabudhe
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Prajakta Sahasrabudhe

Sancheti College of Physiotherapy, Pune

Study Sites (1)

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