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The Effect of Book Reading on Comfort, Hope, Anxiety and Vital Signs of Intensive Care Unit Patients

T

TC Erciyes University

Status

Not yet enrolling

Conditions

Hope
Vital Signs
Anxiety
Comfort

Treatments

Other: Reading a book

Study type

Interventional

Funder types

Other

Identifiers

NCT06465875
2024/147

Details and patient eligibility

About

This study was planned to investigate the effect of reading aloud books on comfort, hope, anxiety and vital signs in patients hospitalized in intensive care unit. This study was designed as a randomized controlled clinical trial. Data will be collected by using the Descriptive Characteristics Questionnaire, General Comfort Scale, Dispositional Hope Scale, State-Trait Anxiety Inventory, and the Vital Signs Monitoring Form.

Full description

This study was planned to investigate the effect of reading aloud books on comfort, hope, anxiety and vital signs in patients hospitalized in intensive care unit. This study was designed as a randomized controlled clinical trial. Data will be collected by using the Descriptive Characteristics Questionnaire, General Comfort Scale, Dispositional Hope Scale, State-Trait Anxiety Inventory, and the Vital Signs Monitoring Form. Individuals in the intervention group will be read a storybook for 3 nights in the intensive care unit. The control group will not be subjected to any practice other than the routine practices of the clinic.

Enrollment

70 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Over 18 years of age,
  2. Stable clinical condition after intensive care unit admission,
  3. Have no physical or mental impairment in answering the questions,
  4. No verbal communication disability (hearing and speech),
  5. No diagnosed psychiatric disorder,
  6. With a Glasgow Coma Scale score of 15,
  7. Not receiving sedation for at least 12 hours,
  8. Will be hospitalized for at least 3 days from the time of enrollment in the study,
  9. Individuals who agree to participate in the study will be included in the study.

Exclusion criteria

  1. People with hearing or vision problems,
  2. Intubated,
  3. Any diagnosed neurological or psychological disorder,
  4. Transferred to another unit or exitus before the specified period,
  5. Individuals who do not agree to participate in the study will not be included in the study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

Intervention group
Experimental group
Description:
The intervention group will be read a storybook for three nights outside the routine practices of the clinic.
Treatment:
Other: Reading a book
Control group
No Intervention group
Description:
The control group will not be subjected to any practice other than the routine practices of the clinic.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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