Clinical Trials Directory

Trials / Completed

CompletedNCT06801145

The Effect of Video-supported Education on Anxiety Levels and the ICU Experience

The Effect of Video-supported Education About the Intensive Care Process on Anxiety Levels and the ICU Experience of Patients Scheduled for Open-heart Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
110 (actual)
Sponsor
Zeynep Turak · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study was conducted to examine the effects of video-assisted education about the intensive care process on intensive care experiences and anxiety levels of patients scheduled for open-heart surgery. Research Hypotheses H01: Video-assisted education regarding the intensive care process provided to patients undergoing open heart surgery does not affect their experiences of intensive care. H1: Video-assisted education regarding the intensive care process provided to patients undergoing open heart surgery does affect their experiences of intensive care. H02: Video-assisted education regarding the intensive care process provided to patients undergoing open heart surgery does not affect patients' anxiety levels. H2: Video-assisted education regarding the intensive care process provided to patients undergoing open heart surgery does affect patients' anxiety levels.

Detailed description

The study will include an experimental and a control group. Patients in the experimental group will be administered the Patient Introduction Form, Trait Anxiety and State Anxiety Scales 48 hours before surgery. Then, video-assisted training will be given about the intensive care process, and the state anxiety scale will be applied again 24 hours before the surgery. Twenty-four hours after discharge from the intensive care unit to the clinic, the State Anxiety Scale and Intensive Care Experience Scales will be applied again. These scales will also be applied to patients in the control group who did not receive video-assisted education. Control group patients will not receive any intervention other than standard nursing care.

Conditions

Interventions

TypeNameDescription
OTHEREducation with VideoPatients in the experimental group will be trained by the researcher 48 hours before the surgery with a video providing information about the intensive care process.

Timeline

Start date
2023-10-01
Primary completion
2024-01-30
Completion
2024-06-30
First posted
2025-01-30
Last updated
2025-12-15

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT06801145. Inclusion in this directory is not an endorsement.