- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05791903
The Effect of Nursing Care Based on Kolcaba's Comfort Theory on of Intensive Care Patients
June 12, 2024 updated by: Ebubekir Kaplan, Istanbul University - Cerrahpasa (IUC)
The Effect of Nursing Care Based on Kolcaba's Comfort Theory on The Comfort, Satisfaction and Sleep Quality of Intensive Care Patients
Nurses aim to care for people who can no longer carry out their life activities and needs, and to ensure that they can continue to live their lives as well as possible.
The aim is to improve the quality of life by making life more comfortable through care.
Comfort in care means solving the patient's problems, being peaceful and content, and relieving pain/suffering.
Kolcaba explained that comfort theory can be used as a guide to meet the comfort needs of individuals in the care process.
The theory explains the concept of comfort as relaxation, refreshment and the ability to overcome problems (superiority).
According to this theory, the nurse identifies the comfort needs of the patient and family and plans and implements interventions to meet these needs.
There are no studies in the literature that have investigated the effect of nursing care based on Kolcaba's comfort theory on the comfort, satisfaction and sleep quality of ICU patients.
The aim of this study is to determine the effect of nursing care based on Kolcaba's Comfort Theory on the comfort, satisfaction and sleep quality of ICU patients.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study is a randomised controlled experimental study to determine the effect of nursing care based on Kolcaba's comfort theory on comfort, care satisfaction and sleep quality of intensive care patients.
Power analysis was used to determine the sample size of the study.
As a result of the power analysis, it was determined that a total of 44 participants, 22 participants in each group, should be reached to achieve 80% power with an effect size of 0.87, a margin of error of 0.05% and a confidence interval of 0.95%.
To increase the reliability of the study, a total of 80 participants, 40 in the intervention group and 40 in the control group, should be included in the study, taking into account data loss.
In this study, the control group will receive standard care and the intervention group will receive care based on Kolcaba's comfort theory.
Data will be collected using the General Comfort Scale, the Newcastle Satisfaction Scale, the Richard Campbell Sleep Scale and the Comfort Behaviours Checklist.
Study Type
Interventional
Enrollment (Actual)
80
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
-
-
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Van, Turkey, 65100
- Van Yuzuncu Yıl University
-
-
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
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Volunteering to participate in the research,
- 18 years of age or older,
- Being open to communication,
- Clear state of consciousness
- Staying in the intensive care unit for at least 24 hours
Exclusion Criteria:
- The patient is taking sedative medication
- Being diagnosed with a sleep disorder,
- The use of sleeping pills,
- Loss of hearing and/or vision
- Use of a hearing aid
- Dependence on mechanical ventilator
- illiteracy
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
In the application process, individuals in the experimental group will receive care based on Kolcaba's comfort theory and comfort behaviour checklist during their stay in the ICU.
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Comfort-orientated care
|
|
No Intervention: Control Group
In this study, the control group will receive standard care.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
General Comfort Scale
Time Frame: 24 hours later
|
The scale, which was developed by Katharine Kolcaba in 1992 in order to determine the comfort needs of individuals, to evaluate the nursing initiatives that can provide comfort and the increase in comfort, was adapted to Turkish society by Kuğuoğlu and Karabacak in 2004.The scale, which is a four-point Likert-type scale with 48 items, was created by guiding the taxonomic structure consisting of the theoretical components of comfort, including 3 levels and 4 dimensions.
Level; While the dimension is evaluated as relief (16 items), relief (17 items) and overcoming the problems (15 items); It is evaluated in three parts: physical (12 items), psychospritual (13 items) and socio-cultural (10 items).
Negative expressions in the scale are calculated by reverse coding during the evaluation phase.
While the lowest total score that can be obtained from the scale is 48, the highest total score is 192.
|
24 hours later
|
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Comfort Behaviors Checklist
Time Frame: 24 hours later
|
The Comfort Behaviour Checklist was developed by Katharina Kolcaba in 1989.
The checklist is completed by the observer when it is not possible for the person to complete the questionnaire.
The Comfort Behaviour Checklist consists of 30 behavioural indicators.
In addition to these, Kolcaba suggests that if the checklist is the only tool used to measure comfort, the individual should give a numerical score for pain and comfort so that comfort can be objectively assessed.
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24 hours later
|
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Richard-Campbell Sleep Scale
Time Frame: 24 hours later
|
The scale was developed by Richards et al. (1987) to assess sleep quality in intensive care units (Richards, 1987; Richards et al., 2000).
The RQAS includes six items (depth of sleep, time to fall asleep, frequency of awakening, duration of wakefulness, quality of sleep and ambient noise level).
The scale score is evaluated with the sum of the first five items.
A score of 25 and below indicates very poor sleep, while a minimum score of 76 and above indicates very good sleep.
|
24 hours later
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Study Director: Aylin ÖZAKGÜL, PhD, Istanbul University - Cerrahpasa (IUC)
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)
May 3, 2023
Primary Completion (Actual)
July 5, 2023
Study Completion (Actual)
June 6, 2024
Study Registration Dates
First Submitted
March 7, 2023
First Submitted That Met QC Criteria
March 17, 2023
First Posted (Actual)
March 30, 2023
Study Record Updates
Last Update Posted (Actual)
June 13, 2024
Last Update Submitted That Met QC Criteria
June 12, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Ebkrkpln
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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