The Effect of Light on Sleep Quality and Physiological Parameters in Individuals in Intensive Care Unit

December 11, 2020 updated by: Kübra Pamuk, Istanbul University - Cerrahpasa (IUC)

The research was carried out in randomized controlled experimental type in order to determine the effect of light in ICU on patients' sleep quality and physiological parameters. The cases were assigned to the experimental and control groups according to the simple randomization method.

The research universe; Between May 2019 and December 2019, sick individuals who were admitted to the 5 isolation rooms in the Reanimation Intensive Care clinic in the education and research hospital in Istanbul were formed. The research sample is; As a result of the power made for the study to be experimentally designed; a total of 148, with a minimum of 74 for each group. In collecting data; Patient Information Form, Numerical Pain Rating Scale, Richards Campbell Sleep Scale, Glaskow Coma Scale, Richmond Agitation Sedation Scale, Bedside Monitors were used to measure physiological parameters. The data obtained as a result of the research were made using the package program named SPSS (IBM SPSS Statistics 24).

Study Overview

Detailed Description

Sleep causes temporary, partial and periodic interruption of the organism's interaction with the environment, is a physiological condition that affects many systems. That sleep activity is a vital and important activity for individuals.They emphasized and sleep; the alternating state of inertia and inertia, around the human a situation where they do not respond to the events that took place. initiation and maintenance through the function of many cortical and subcortical brain regions. People sleep on average one third of their lives They spend it. The sleep of a normal adult person consists of night sleep and It lasts an average of 7 to 9 hours, with a sleep time of four to six 90 to 100 minutes. Non-REM (NREM) and REM sleep change cyclically. In the sleep-wake cycle in man, the most basic and determinant is the circadian rhythm. Circadian The rhythm refers to changes in the physiological and biological processes of the organism for about a day. The main center that regulates the circadian rhythm is located in the anterior hypothalamus as a double structure. suprachiasmatic nucleus (SKN). Light is the most important rhythm editor. Other regulators are social and are physical activities. Florence Nightingale and Virgina Henderson in love and day rhythm; defined the patient as two important factors in supporting the health of the individual. In the regulation of the circadian rhythm, the light and dark cycle in the external environment is important. The synthesis and release of melatonin is stimulated in the dark at night, and during the day by the effect of light It is suppressed. N-acetyl transferase (NAT) enzyme is effective in melatonin formation. Melatonin The main task of the hormone is to protect the biological rhythm of the body. In this context; lighting, circadian rhythm and sleep are related.

Health care institutions and especially intensive care units, in terms of physical environment and lighting the patient can affect the circadian rhythm of the individual, change the release of melatonin and as a result can affect sleep patterns and cognitive performance. In our country, in terms of physical environment lighting, it does not support circadian rhythms. As a result, sick individuals in the ICU are asleep The therapeutic effect of sleep because they spend a significant amount of time they need to be awake can not benefit sufficiently. In addition, in the ICU, many There is a factor. These factors are; pain, physical condition, drug therapy, fear of death, environmental noise, pleasant non-smells, invasive interventions, loss of privacy and family disability. In the study of, the greatest stress of the sick individuals in the ICU One of the causes was found to be sleeping problems. In the literature, especially in health care institutions In patients with ICU inpatient, sleep activity has a negative effect on both duration and quality. shows that it is affected In admission to the ICU, when environmental factors are not suitable, the patient especially the sleep activity of the individual is impaired and this process occurs even after the patient is discharged from YBU, can continue. One of the biggest reasons for this; Physical environment and lighting of ICUs in terms of disruption of circadian rhythms of sick individuals. The presence of night light suppresses the level of melatonin, which is normally the highest at night. Melatonin level is accepted as an indicator of circadian rhythm. Artificial lighting is a known factor in the disruption of the circadian rhythm. Sick individuals in the ICU, 24 hours it is exposed to artificial light throughout a cycle. Artificial lighting, health of the sick individual health care to help professionals continue their care and treatment practices It is applied at high levels for 24 hours in institutions such as ICU. Its as a result, daylight is often obscured / eliminated in ICUs and artificial lighting are added. Researches conducted, unnatural night disruption of circadian rhythms with illumination causes health problems related to sleep activity. It is also sufficient and relaxing non-sleep, negatively affects the immune system, wound healing process and cognitive functions of the sick individual. It affects in the same direction, increases the level of stress and delays its recovery. Sick individuals in the ICU are concerned with serious illnesses or injuries and care and treatment. The illness of the symptoms lies. Today, long-term health of an illness or injury in an ICU It is known to cause problems. Some of these problems are sleep problems due to lighting and circadian rhythm disturbances. our Country Study to determine the effect of environmental factors related to lighting on sleep problems in ICU There is. Nurses who continue the care and treatment of sick individuals in ICU, diagnosing problems early, identifying primary nursing diagnoses, existing stressors important role such as reduction, ensuring the necessary environmental regulation to create a therapeutic environment, and they have responsibilities. In this context, this research is based on YBU. to determine the effect of light on sleep quality and physiological parameters in individuals and nursing will be carried out to guide its applications.

Study Type

Interventional

Enrollment (Actual)

148

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

      • Istanbul, Turkey
        • Istanbul Education Research Hospital

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 88 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 18 years of age or older,
  • Not having a problem in terms of consciousness and sense organs
  • A score of 9 or above on the Glaskow Coma Scale (GCS),
  • Richmond Agitation-Sedation Scale (RASS) score was determined as -1,0,1.

Exclusion Criteria:

  • Be under the age of 18
  • Having a problem in terms of consciousness and sense organs,
  • A GCS score below 9,
  • Receiving inotropic support,
  • Being fully sedated,
  • Having a chronic disease such as chronic heart disease, dementia, psychosis,
  • Identified as having severe brain injury.

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Individual Characteristics of the Individuals in the Experimental and Control Groups
The personal characteristics of the individuals included in the study were examined.
General characteristics of the individuals in the experimental and control groups were compared.
Active Comparator: Disease Characteristics of the Individuals in Experimental and Control Groups
The intensive care experience of the individuals included in the study, their status of receiving respiratory support, and the reason for staying in the intensive care unit were explained.
General characteristics of the individuals in the experimental and control groups were compared.
Active Comparator: Distribution of Findings Regarding Sleep Activity of the Individuals in Both Groups
The personal characteristics of the individuals in the experimental and control groups regarding sleep were examined.
General characteristics of the individuals in the experimental and control groups were compared.
Active Comparator: Comparison of the Individuals in the experimental and control groups after 24 hours of sleep
The effect of light after 24 hours in the experimental and control groups of individuals hospitalized in the intensive care unit was examined.
According to the results of randomization, the group to which the lighting system will be applied was assigned as "experiment", and the group that will continue standard ICU lighting as "control"
Active Comparator: Comparison of physiological parameters of individuals in both groups after 24 hours
Comparison of the physiological parameters of the individuals in the experimental and control groups 24 hours after their admission to the ICU.
According to the results of randomization, the group to which the lighting system will be applied was assigned as "experiment", and the group that will continue standard ICU lighting as "control"
Active Comparator: Comparison of the Sleep Times of the Individuals in Both Groups 48 Hours After Intensive Care
The effect of light after 48 hours in the experimental and control groups of individuals hospitalized in the intensive care unit was examined.
According to the results of randomization, the group to which the lighting system will be applied was assigned as "experiment", and the group that will continue standard ICU lighting as "control"
Active Comparator: Comparison of physiological parameters of individuals in both groups after 48 hours
Comparison of the physiological parameters of the individuals in the experimental and control groups 48 hours after their admission to the ICU.
According to the results of randomization, the group to which the lighting system will be applied was assigned as "experiment", and the group that will continue standard ICU lighting as "control"
Active Comparator: Distribution of Total Sleep Times of the Individuals in the Experimental and Control Groups
The sleep times of the individuals in both groups were compared
According to the results of randomization, the group to which the lighting system will be applied was assigned as "experiment", and the group that will continue standard ICU lighting as "control"

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in sleep time with light intervention in experimental and control groups in the intensive care unit
Time Frame: After the patient was admitted to the intensive care unit, 48 hours of sleep time was recorded.
A recirculating lighting system was installed in the isolation room for the experimental group in line with evidence-based design principles. Light fixture 120 cm from the floor. high and light shining up. The system was set up to operate at varying levels of 9 lights, illumination for 24 hours. No application other than the standard lighting system of the ICU was applied to the individuals in the control group. Actiwatch device was placed on the arm of the sick individuals. Thanks to this device, the sleep time of the individuals was recorded.
After the patient was admitted to the intensive care unit, 48 hours of sleep time was recorded.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The effect of light on the patient's systolic and diastolic blood pressure in the experimental and control groups in the intensive care unit.
Time Frame: The systolic and diastolic blood pressure of the patient who was admitted to the intensive care unit was recorded for 48 hours.
The systolic and diastolic blood pressure of the individual was recorded hourly by the investigator through the bedside monitoring system for 48 hours after admission to the ICU.
The systolic and diastolic blood pressure of the patient who was admitted to the intensive care unit was recorded for 48 hours.
The effect of light on patient's heart rate in intensive care unit in experimental and control groups.
Time Frame: The heart rate of the patient, who was admitted to the intensive care unit, was recorded for 48 hours.
The heart rate of the individual was recorded hourly by the researcher through the bedside monitoring system for 48 hours after admission to the ICU.
The heart rate of the patient, who was admitted to the intensive care unit, was recorded for 48 hours.
The effect of light on patient's respiratory rate in intensive care unit in experimental and control groups.
Time Frame: The respiration of the patient who was admitted to intensive care unit was recorded for 48 hours.
The respiration of the patient was recorded hourly by the researcher through the bedside monitoring system for 48 hours after admission to the ICU.
The respiration of the patient who was admitted to intensive care unit was recorded for 48 hours.
The effect of light on the patient's body temperature in the intensive care unit in the experimental and control groups.
Time Frame: The body temperature of the patient who was admitted to intensive care unit was recorded for 48 hours.
The body temperature of the patient was recorded hourly by the researcher through the bedside monitoring system for 48 hours after admission to the ICU.
The body temperature of the patient who was admitted to intensive care unit was recorded for 48 hours.

Collaborators and Investigators

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

Investigators

  • Principal Investigator: kübra pamuk, graduate, 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 2, 2019

Primary Completion (Actual)

July 5, 2019

Study Completion (Actual)

December 28, 2019

Study Registration Dates

First Submitted

November 11, 2020

First Submitted That Met QC Criteria

December 7, 2020

First Posted (Actual)

December 14, 2020

Study Record Updates

Last Update Posted (Actual)

December 16, 2020

Last Update Submitted That Met QC Criteria

December 11, 2020

Last Verified

November 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • U1111-1260-6250
  • Kübra pamuk (Other Identifier: Istanbul University-Cerrahpasa)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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