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Clinical Trials/NCT05088044
NCT05088044UnknownNot Applicable

A Quasi Experimental Study to Assess the Impact of Implementing Modified Early Warning Score in Terms of Competency and Self-efficacy of Nurses at ILBS, Delhi

Institute of Liver and Biliary Sciences, India1 site in 1 country82 target enrollmentStarted: November 11, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
82
Locations
1
Primary Endpoint
to assess the impact of MEWS on competency and self-efficacy of nurses before and after implementing MEWS

Study Overview

Brief Summary

In this study nurses will be taught regarding Modified Early Warning Score and how to mark the involved physiological parameters in the MEWS chart and then scoring will be given i.e MEWS score and according to the score intervention would be taken by nurses by communicating with other health team members. this scoring will allow nurses to assess early deterioration and early ICU admission and at last nurses will be asked regarding the barriers or facilitators they faced while performing MEWS score.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
21 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •registered nurses working in general, semi-private and private ward nurses willing to participate

Exclusion Criteria

  • •registered nurses who will not be present at the time of data collection. pull out staffs.

Arms & Interventions

staff nurses

Experimental

firstly pre-test would conducted for the group then after 7 days post-test would be conducted for the same group intervention which will be given: training on modified early warning score to staff nurses and marking of physiological parameters on MEWS chart

Intervention: training porogram (Other)

Outcomes

Primary Outcomes

to assess the impact of MEWS on competency and self-efficacy of nurses before and after implementing MEWS

Time Frame: 7 days

pre-test would be taken to assess previous level and post-test to measure the change in competency

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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