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Clinical Trials/CTRI/2024/07/069913
CTRI/2024/07/069913
Not yet recruiting
Not Applicable

A quasi experimental study to assess the effectiveness and feasibility of using Modified Early Warning Signs (MEWS)score on early detection of adverse cardiac signs on selected outcome variables among cardiac patients in Advanced Cardiac Centre, PGIMER, Chandigarh,2023 – 25

VANITHA A1 site in 1 country154 target enrollmentStarted: July 17, 2024Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
VANITHA A
Enrollment
154
Locations
1
Primary Endpoint
Checking the feasibility of using MEWS score among the cardiac patients and its effectiveness, patient safety and quality of care

Overview

Brief Summary

A quasi experimental design is using to identify the feasibility and effectiveness of Modified Early Warning Signs (MEWS) score among the cardiac patients by estimated sample size of 154. In which experimental group 77 and control group will be 77. Control group will receive the as usual routine care where as experimental group will monitored with the help of MEWS score and with routine care. Assessing the outcome variables such as feasibility, timely initiation of treatment, care escalation, patient safety and quality of care and also assessing the in hospital cardiac arrest.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 90.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • includes the both adult male and female from the age group of 18 years with the selected cardiac patients who are all under high risk of deterioration.

Exclusion Criteria

  • for this study includes the selected cardiac patients below 18 years of age and the cardiac patients who died within 24 hours of admission and the patients who had cardiac arrest at the time of admission.

Outcomes

Primary Outcomes

Checking the feasibility of using MEWS score among the cardiac patients and its effectiveness, patient safety and quality of care

Time Frame: 6 Weeks

Secondary Outcomes

  • Assessing the care escalation, in hospital cardiac arrest & timely intervention initiation(6Weeks)

Investigators

Sponsor
VANITHA A
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

VANITHA A

Department of Nursing, National Institute of Nursing Education, PGIMER, Chandigarh -160012

Study Sites (1)

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