CompletedNot Applicable

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

Turkey (Türkiye)110 participantsStarted 2023-10-01

Plain-language 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.

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: * Patients aged 18 and over, * 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 who did not volunteer to participate, * 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.

What they're measuring

Intensive care experience

Timeframe: 24 hours after arriving from intensive care care

Anxiety level

Timeframe: 48 hours before surgery, 24 hours before surgery, 24 hours after intensive care unit

Trial details

NCT IDNCT06801145

SponsorZeynep Turak

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-01-30