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Impact of Immersive Video Education on Cardiothoracic Surgery Anxiety and Outcomes

Exploring the Effect of Visually Immersive Video Education on Cardiothoracic Surgery Patients' Preoperative Anxiety and Postoperative Outcomes

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07222839
Enrollment
200
Registered
2025-10-30
Start date
2026-01-15
Completion date
2027-01-15
Last updated
2026-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety

Brief summary

The purpose of this quasi-experimental study is to examine the effect of visually immersive preoperative education on levels of anxiety and patient outcomes in patients undergoing cardiothoracic (open heart) surgery

Interventions

BEHAVIORALVisually Immersive Video

The patients watch a 5-minute visually immersive education video on what to expect postoperatively on arrival to the cardiovascular intensive care unit (CVICU) followed by the opportunity for discussion/explanation and questions.

BEHAVIORALStandard of Care

The patient receives a basic verbal explanation of what to expect postoperatively on arrival to CVICU followed by the opportunity for questions.

Sponsors

Baptist Health South Florida
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Inpatients and outpatients scheduled for elective cardiothoracic (open heart) surgery

Exclusion criteria

* Patients undergoing emergent cardiothoracic (open heart) surgery * Patients with altered mental status * History of mental health disorders (schizophrenia and bipolar disorder) * Legally blind/complete blindness and hearing impaired (without hearing aids)

Design outcomes

Primary

MeasureTime frameDescription
Anxiety relief (self-report measure 1 - State-Trait Anxiety Inventory)30 minutesPatient's anxiety will be measured using the 20-item State-Trait Anxiety Inventory (STAI) (state scale only) (higher scores indicate higher anxiety), taken before and after preoperative education is received.
Anxiety relief (self-report measure 2 - Visual Analog Scale for Anxiety)30 minutesPatient's anxiety will be measured using the Visual Analog Scale for Anxiety (VAS-A), a slider scale of 0 - 100 is used to self-report anxiety (0 = not anxious and 100 = extremely anxious), taken before and after preoperative education is received.

Secondary

MeasureTime frameDescription
Postoperative CVICU Outcome 2 - Intubation TimeWithin 30 days after the patient is discharged from CVICUIntubation time = Length of time the patient is on mechanical ventilation.
Postoperative CVICU Outcome 3 - Re-intubationWithin 30 days after the patient is discharged from CVICURe-intubation after initial removal from mechanical ventilation (yes or no).
Postoperative CVICU Outcome 4 - Blood Sugar RegulationWithin 30 days after the patient is discharged from CVICUBlood sugar regulation = comparison of point-of-care blood sugar levels taken on postoperative day 1 and on the day of discharge from CVICU.
Anxiety relief (physiological measure 1 - blood pressure)30 minutesBlood pressure is measured before and after receipt of preoperative education. Increased anxiety may cause elevation of this physiological indicator.
Anxiety relief (physiological measure 3 - respiratory rate)30 minutesRespiratory rate is measured before and after receipt of preoperative education. Increased anxiety may cause elevation of this physiological indicator.
Anxiety relief (physiological measure 2 - heart rate)30 minutesHeart rate is measured before and after receipt of preoperative education. Increased anxiety may cause elevation of this physiological indicator.
Postoperative CVICU Outcome 1 - Length of StayWithin 30 days after the patient is discharged from CVICUPatients' length of stay (# days) in the CVICU.

Countries

United States

Contacts

STUDY_CHAIRNatalie Bermudez, PhD, RN, EBP-C

Baptist Health | Nursing & Health Sciences Research

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026