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

Anxiety Clinical Trial

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06465875
• Other study ID #: 2024/147
• Status: Not yet recruiting
• Phase: N/A
• Start date: July 1, 2024
• Est. completion date: December 31, 2024

Study information

• Verified date: June 2024
• Source: TC Erciyes University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

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.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 70
• Est. completion date: December 31, 2024
• Est. primary completion date: October 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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.

Related Conditions & MeSH terms

• Anxiety
• Anxiety Disorders
• Comfort
• Hope
• Vital Signs

Intervention

Other:
• Reading a book
Individuals in the intervention group will be read a storybook for three nights.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
TC Erciyes University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Comfort level to be evaluated with the General Comfort Scale	It was developed to assess the comfort level of patients. The scale consists of three levels: relief, relaxation and superiority and four dimensions: physical, psychospiritual, sociocultural and environmental.	After reading the book of the 3rd day
Primary	Level of hope to be assessed with the Dispositional Hope Scale	It was conducted to evaluate individuals' hope levels. It is an eight-point Likert type scale consisting of 12 items. Scores from the scale vary between 8 and 64.	After reading the book of the 3rd day
Primary	Anxiety level to be assessed with State-Trait Anxiety Inventory	The inventory was developed to determine the state and trait anxiety levels of individuals. The scale consists of 40 items in total. While the first 20 items measure the state anxiety level, the items from 21 to 40 measure the trait anxiety level of the individual. The total score value obtained from both parts varies between 20 and 80.	After reading the book of the 3rd day
Secondary	Blood pressure to be assessed with monitor	The patient's blood pressure will be measured from the brachial artery with a bedside monitor and the result will be recorded in mmHg.	After reading the book of the 3rd day
Secondary	Pulse to be assessed with monitor	Heart rate will be measured with a bedside monitor that can be measured from a finger and recorded as beats/min.	After reading the book of the 3rd day
Secondary	Oxygen saturation to be assessed with Pulse Oximeter	Oxygen saturation from the finger will be measured and recorded with a Pulse Oximeter.	After reading the book of the 3rd day
Secondary	Pain to be assessed with Numeric Rating Scale	The number "0" on the scale means that they do not feel any pain and the number "10" refers to the worst pain.	After reading the book of the 3rd day