The Effect of Eye Mask and Music on Sleep Quality and Delirium in Patients Monitored in Intensive Care Unit

T

TC Erciyes University

Status

Enrolling

Conditions

Abdominal Surgery

Treatments

Behavioral: Eye patch

Study type

Interventional

Funder types

Other

Identifiers

NCT06268158
2023/45

Details and patient eligibility

About

After abdominal surgery, most patients experience problems such as respiratory complications, surgical wound infection, cardiac problems, renal failure, delirium, and insomnia, along with surgical trauma and underlying comorbidities. Postoperative delirium (POD) is an adverse postoperative complication that can occur in patients of all ages, from children to the elderly. Effective non-pharmacological treatment approaches for delirium include using an orientation board, calendar, clock, ensuring hydration, improving sleep quality, therapeutic activities, providing companionship of family members, and building private rooms. This study will be conducted as a randomized controlled and experimental study to determine the effect of eye patch and music on sleep quality and delirium in patients followed after abdominal surgery in the surgical intensive care unit. It was planned to include a total of 34 patients who underwent abdominal surgery, 17 in the experimental group and 17 in the control group. During the data collection phase, the Patient Information Form, Richard-Campbell Sleep Scale, Nursing Delirium Screening Scale and Richmond Agitation-Sedation Scale, will be used.

Enrollment

34 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Those who have had abdominal surgery
  • Those who volunteer to participate in the research
  • Those who are over 18 years old
  • Richmond Agitation-Sedation Scale -1, 0, +1
  • Those who have been in intensive care for at least 3 days
  • No communication problems (language, hearing impairment, etc.)
  • No mental problems
  • Patients who do not use sleeping pills or sedating drugs and who do not have alcohol or substance addiction will be included in the study.

Exclusion criteria

  • Those who experience blood loss and fluid electrolyte imbalance after surgery
  • There are contraindications to the use of eye masks (for example, head trauma),
  • Patients with delirium before or after surgery will not be included in the study.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

34 participants in 2 patient groups

Intervention group
Experimental group
Description:
Patients in the experimental group will wear an eye patch after 22:00, when clinical interventions are less frequent, and will be listened to calming music once a day for 1 hour for 3 days.
Treatment:
Behavioral: Eye patch
Control group
No Intervention group
Description:
No treatment will be performed on patients in the control group outside of their clinical routine.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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