- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07100002
- Original Trial
Comparing the Efficacy of Earplugs and Eye Masks on Pain and Sleep Quality
Comparing the Efficacy of Earplugs and Eye Masks on Pain and Sleep Quality in Cardiovascular Intensive Care Unit Patients: A Three-Arm Randomized Controlled Trial
Objective: To determine the superiority of earplugs and eye masks to each other and their efficacy in pain and sleep quality.
Methods: The study was a three-arm randomised controlled trial. After a baseline assessment, participants were randomly assigned in three groups. The random assignment was performed by using a computer program (Microsoft Excel 2016). Afterward, participants were categorized into three subgroups. Group 3 patients in this group did not receive any treatment to improve pain and sleep quality during the study period. Routine postoperative care was applied in the clinic (n = 25). Group 2 was applied the earplug (n = 25), whereas Group 1 was applied the eye mask (n = 24).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Piraziz
-
Giresun, Piraziz, Turkey, 28000
- Giresun Üniversitesi
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged 18 and older,
- Having undergone first and elective cardiac surgery, literate, and having no verbal communication skills.
- The participants who stayed in the ICU for 48 hours after surgery, had an ASA (American Society of Anesthesiologists) Score of I or II, and had no visual or audial problems were also included in the study.
Exclusion Criteria:
- Exclusion criteria for the study participants were refusing to use an eye mask or earplug, having early complications or re-surgery history, having reintubation after extubation, having any intra-aortic balloon pump or cardiac pacemaker, and taking inotropic drugs in the ICU.
- Patients refusing to use an eye mask or earplugs were also excluded from the study. Additionally, patients who had a history of chronic pain, alcohol or drug dependency, psychiatric disease, chronic sleep disorders, anxiolytic or sleeping medication use, and claustrophobia.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Control Group
|
Patients in this group did not receive any treatment to improve pain and sleep quality during the study period.
Routine postoperative care was applied in the clinic.
|
|
Experimental: Earplug Group
Patients who met the inclusion criteria were fitted with standard earplug of the same brand by the researcher at night.
The researcher applied the earplug from 01:00 AM to 05:00 AM.
The reason for this is that the procedures performed on the patients within the clinical routine ended at 01:00 AM and the patients' uninterrupted sleep hours coincided with these hours.
|
Patients who met the inclusion criteria were fitted with standard earplug of the same brand by the researcher at night.
The researcher applied the earplug from 01:00 AM to 05:00 AM.
The reason for this is that the procedures performed on the patients within the clinical routine ended at 01:00 AM and the patients' uninterrupted sleep hours coincided with these hours.
|
|
Experimental: Eye mask Group
Patients who met the inclusion criteria were fitted with standard eye masks of the same brand by the researcher at night.
The researcher applied the eye mask from 01:00 AM to 05:00 AM.
The reason for this is that the procedures performed on the patients within the clinical routine ended at 01:00 AM and the patients' uninterrupted sleep hours coincided with these hours.
|
Patients who met the inclusion criteria were fitted with standard eye masks of the same brand by the researcher at night.
The researcher applied the eye mask from 01:00 AM to 05:00 AM.
The reason for this is that the procedures performed on the patients within the clinical routine ended at 01:00 AM and the patients' uninterrupted sleep hours coincided with these hours.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postoperative sleep quality
Time Frame: 6 month
|
Sleep quality was assessed using the Richard Campbell Sleep Questionnaire.
|
6 month
|
|
Postoperative pain severty
Time Frame: 6 month
|
Pain was assessed using the Visual Analyses Scale.
|
6 month
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Giresun Üniversitesi
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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