Effectiveness of Mindfulness Based Meditation on Well-being, Self Compassion & Cognizance Among Nurses Working in Intensive Care Units

September 30, 2020 updated by: Institute of Liver and Biliary Sciences, India

A Pre-Experimental Study to Assess the Effectiveness of Mindfulness Based Guided Meditation on Wellbeing, Self Compassion and Cognizance Among Nurses Working in Intensive Care Units at ILBS, New Delhi

Effect of Mindfulness Based Guided Meditation on Intensive care Unit nurses wellbeing,cognizance & self compassion was assessed .

Study Overview

Detailed Description

: Primary objective To assess the Effectiveness of Mindfulness Based Guided Meditation on Wellbeing, Self Compassion and Cognizance among Nurses working in Intensive Care Units at ILBS.

Hypothesis

The following hypothesis will be tested at 0.05 level of significance:

H1There will be a significant difference between pretest Wellbeing scores and posttest Wellbeing scores of Nurses working in Intensive Care Units. H2There will be a significant difference between pretest Self Compassion Scores and posttest Self Compassion scores of Nurses working in Intensive Care Unit.

H3There will be a significant difference between pretest Cognizance Scores and posttest Cognizance score of Nurses Working in Intensive Care Units.

H4 There will be a significant relationship between Wellbeing and Self Compassion Among Nurses working in Intensive Care Units.

H5 There will be a significant relationship between Wellbeing and Cognizance among Nurses working in Intensive Care Units.

H6 There will be a significant relationship between Self Compassion and Cognizance Among Nurses working in Intensive Care Units.

H7 There will be a significant association of posttest wellbeing score with selected Socio demographic variables of Nurses working in Intensive Care Units.

H8 There will be a significant association of posttest Self Compassion score with selected sociodemographic variables of Nurses working in Intensive Care Units.

H9 There will be a significant association of Posttest Cognizance score with selected sociodemographic variables of Nurses working in Intensive Care Units.

Research Design Pre-experimental, one group pre test -post test design

Study Type

Interventional

Enrollment (Actual)

61

Phase

  • Not Applicable

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

    • Haryana
      • Faridabad, Haryana, India, 121001
        • Neetu Taneja

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Registered nurses who were Working in ICUs for at least last three months continuously.

Exclusion Criteria:

  • Registered nurses who were On long leave Had joined recently in ICUs

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

  • Primary Purpose: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental
Mindfulness Based Guided Meditation
Mindfulness Based Guided Meditation will be practiced by nurses under the supervision of researcher for 15 min thrice a week for two weeks

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Wellbeing
Time Frame: 10 minutes
The study will be carried out among Nurses working in Intensive Care Units at ILBS Hospital using Total enumeration technique. The primary outcome measure will be increase in post test wellbeing scores among nurses as compared to their pretest wellbeing scores which will be assessed by using Warwick Edinburgh Mental Wellbeing scale in about 10 mins.
10 minutes
Self Compassion
Time Frame: 15 minutes
The study will be carried out among Nurses working in Intensive Care Units at ILBS hospital using Total enumeration technique.The primary outcome measure will be increase in post test Self Compassion scores among nurses as compared to their pre test Self Compassion scores which will be measured using Self Compassion Scale in about 15 mins.
15 minutes
Self Compassion
Time Frame: 10 minutes
The study will be carried out among Nurses working in Intensive Care Units at ILBS hospital using Total enumeration technique. The primary outcome measure will be increase in post test Cognizance score among nurses as compared to their pretest Cognizance scores which will be measured using Mindful Attention Awareness Scale in about 10 mins
10 minutes

Collaborators and Investigators

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

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)

June 14, 2019

Primary Completion (Actual)

October 30, 2019

Study Completion (Actual)

October 30, 2019

Study Registration Dates

First Submitted

July 22, 2020

First Submitted That Met QC Criteria

September 30, 2020

First Posted (Actual)

October 1, 2020

Study Record Updates

Last Update Posted (Actual)

October 1, 2020

Last Update Submitted That Met QC Criteria

September 30, 2020

Last Verified

November 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • F15(2/2.25)/2017/HO(M)/ILBS

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.

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