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The Effect of Informing Patients With Video Surgery

The Effect of Informing Patients With Video on Intensive Care Experiences Before Heart Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05255887
Enrollment
90
Registered
2022-02-25
Start date
2022-09-25
Completion date
2023-03-25
Last updated
2023-08-29

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

Conditions

Cardiovasculary Surgery, Education, Critical Care

Keywords

Cardiovascular surgery, education, critical care

Brief summary

Purpose of the research; The aim of this study is to determine the effect of informing patients with video before heart surgery on their intensive care experience.Patient Descriptive Information Form and Intensive Care Experience Scale (ICES) will be used to collect data.In Kavuncu's study, the average score they got from ICES was found to be 57.07±5.6. It was calculated that 45 patients from each group should be included in the study in order to test the 0.6-unit effect size value, which was calculated by accepting a 5% difference from this score in the experimental group, with a 5% margin of error, 95% confidence level and 80% power value.In the study, after the patients admitted to the cardiovascular surgery service for cardiac surgery were informed about the purpose and importance of the study and the research, informed consent will be obtained verbally and in writing from the volunteer patients. In order to ensure randomization of the patients in the study, a randomization plan was prepared for 45 experiments and 45 controls using a probabilistic scheme-based computer program.

Detailed description

Purpose of the research; The aim of this study is to determine the effect of informing patients with video before heart surgery on their intensive care experience.Patient Descriptive Information Form and Intensive Care Experience Scale (ICES) will be used to collect data.In Kavuncu's study, the average score they got from ICES was found to be 57.07±5.6. It was calculated that 45 patients from each group should be included in the study in order to test the 0.6-unit effect size value, which was calculated by accepting a 5% difference from this score in the experimental group, with a 5% margin of error, 95% confidence level and 80% power value.In the study, after the patients admitted to the cardiovascular surgery service for cardiac surgery were informed about the purpose and importance of the study and the research, informed consent will be obtained verbally and in writing from the volunteer patients. In order to ensure randomization of the patients in the study, a randomization plan was prepared for 45 experiments and 45 controls using a probabilistic scheme-based computer program. 24-48 hours before the surgery, the patients will be shown an informative video about the intensive care environment in a separate room through a one-on-one interview. In the study, no attempt will be made to the control group patients other than the routine practice of the institution before the surgery. In the study, the day of discharge from the intensive care unit will be counted as the first day, and on the second day, the 'Intensive Care Experience Scale' will be applied to the patients in both the experimental and control groups by face-to-face interview method.

Interventions

OTHERInforming Patients With Video

24-48 hours before the surgery, the patients will be shown an informative video about the intensive care environment in a separate room through a one-on-one interview. (The content of the training to be done with the video is stated in the appendix) In the study, no attempt will be made to the control group patients other than the routine practice of the institution before the surgery. In the study, the day of discharge from the intensive care unit will be counted as the first day, and on the second day, the 'Intensive Care Experience Scale' will be applied to the patients in both the experimental and control groups by face-to-face interview method.

Sponsors

Kırklareli University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* 18 years old and above, open to communication and cooperation, * He will have planned heart surgery, * He is sane, * Not having a diagnosis of psychiatric disease or using psychiatric medication, * Do not have sensory problems such as vision, hearing and speech, * Literate, * speaking Turkish, * Patients who volunteered to participate in the study

Exclusion criteria

* Under the age of 18 and not open to communication and cooperation, * Unplanned or emergency heart surgery, * mentally ill * Diagnosed with psychiatric illness and using psychiatric medication, * Having sensory problems such as vision, hearing and speech * Being illiterate * Does not speak Turkish, * Patients who did not volunteer to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
The effect of preoperative video training on patients' intensive care experience1 yearThe Intensive Care Experience Scale will be used for determining the effect of preoperative video training on patients' intensive care experience. According to 19 items with scale, the individual may determine his or her experiences in intensive care unit. The Intensive Care Experiences Scale are scored between 19 and 95. The lowest score that can be obtained from the scale is 19, the highest score is 95. As the total score obtained from the scale increases, it is evaluated that the patient's experience is positive and his awareness is high.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026