Effect of Video Training on Patients' Self-Efficacy After Colorectal Surgery

Ankara Yildirim Beyazıt University

Status: Begins enrollment in 3 months

Conditions: Colorectal Cancer

Treatments: Behavioral: Postoperative management

Study type: Interventional

Funder types: Other

Identifiers

NCT07078656

AnkaraYBU-SBF-GG-01

Details and patient eligibility

About

The purpose of the study is to determine the effect of virtual reality video training on the self-efficacy of patients after colorectal surgery. Thus, correct planning can be provided for trainings that will provide information to patients according to their needs during the nursing care process.

Does virtual reality video training have an effect on participants' perceptions of self-efficacy after colorectal surgery? The researchers will conduct the self-efficacy survey on another group of participants without repeating the training to see the impact of the training.

Participants in the experimental group will receive training on the second postoperative day and they will apply a self-efficacy survey on the tenth day after discharge.

Participants in the control group will not receive training on the second postoperative day. They will complete a self-efficacy survey on the tenth day after discharge.

Full description

The data obtained in the study will be evaluated in a computer environment using the IBM SPSS Version 22.0 package program. The conformity of the data to normal distribution will be assessed using the Kolmogorov-Smirnov test, and if the p value is p<0.05, Skewness and Kurtosis values will be examined. Descriptive statistics will be applied to sociodemographic variables. For intergroup comparisons of pre-test and post-test measurements of the experimental and control groups according to dependent variables, the significance test for the difference between two independent means will be used; for non-parametric data, the Mann Whitney U test will be used. For comparisons of pre-test and post-test measurements within the experimental and control groups according to dependent variables, the t-test for dependent groups will be used; for non-parametric data, the Wilcoxon test will be used. The results will be evaluated at a 95% confidence interval and a significance level of p<0.05.

Enrollment: 66 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

IInclusion Criteria:

• aged 18 and over
• aged 65 and under
• undergoing laparoscopic general surgery under general anesthesia
• with no vision, hearing, or perception problems
• with no communication problems
• without nausea, vomiting, dizziness, etc.
• with an ASA score of I, II, or III
• who voluntarily agreed to participate in the study

Exclusion Criteria:

• who have not undergone laparoscopic surgery
• who are hemodynamically unstable
• with an ASA score of IV
• with neurological or psychological problems
• Emergency and unplanned cases

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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66 participants in 2 patient groups

Virtual Reality Glasses

Experimental group

Description:

Virtual reality glasses are a technological product that provides the human mind with the perception of real space and features of images arranged in a computer environment in 3 dimensions. It is also used as an educational tool, which is widely used in daily entertainment venues.

Treatment:

Behavioral: Postoperative management

Control

No Intervention group

Description:

In the control group, after obtaining permission with the "Informed Consent Form" one day before the surgery, the patients who agreed to participate in the study will fill out the "Patient Introduction Form" by the researchers, they will not receive any intervention and will be provided with routine nursing care provided in the hospital. The "Self-Efficacy Scale" will be applied when the patient comes for a check-up 10 days after discharge.