The Effect of Informing Patients With Video Surgery

Kırklareli University

Status: Completed

Conditions: Cardiovasculary Surgery, Education, Critical Care

Treatments: Other: Informing Patients With Video

Study type: Interventional

Funder types: Other

Identifiers

NCT05255887

KırklareliUU

Details and patient eligibility

About

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.

Full 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.

Enrollment: 90 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

90 participants in 2 patient groups

Informing patients group

Experimental group

Description:

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, 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 the experimental group by face-to-face interview method.

Treatment:

Other: Informing Patients With Video

Control Group

No Intervention group

Description:

patients who were no intervation