The Effect of Video-supported Education on Anxiety Levels and the ICU Experience
NCT ID: NCT06801145
Last Updated: 2025-12-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
110 participants
INTERVENTIONAL
2023-10-01
2024-06-30
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Experimental group
Video training will be provided 48 hours before the surgery.
Education with Video
Patients 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.
Control group
This group will receive no intervention other than the applied scales; only standard nursing care will be maintained.
No interventions assigned to this group
Interventions
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Education with Video
Patients 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.
Eligibility Criteria
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Inclusion Criteria
* Cognitively competent,
* Communicative and cooperative,
* Patients undergoing planned surgery (patients not admitted for emergency surgery),
* Patients without a psychiatric diagnosis,
* Patients with sensory impairments such as vision, hearing, or speech,
* Patients with stable hemodynamic status in the clinic,
* Patients who volunteered to participate in the study were included in the study.
Exclusion Criteria
* Patients whose surgery was canceled,
* Patients who underwent emergency surgery,
* Patients who underwent combined bypass and valve surgery,
* Patients with previous intensive care experience,
* Patients who developed complications before, during, or after surgery were excluded from the study.
18 Years
ALL
No
Sponsors
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Zeynep Turak
OTHER
Responsible Party
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Zeynep Turak
Master student
Locations
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Atatürk University
Erzurum, Yakutiye, Turkey (Türkiye)
Countries
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Other Identifiers
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B.30.2.ATA.0.01.00/363
Identifier Type: -
Identifier Source: org_study_id
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