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

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

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07078656
Enrollment
66
Registered
2025-07-22
Start date
2026-06-30
Completion date
2026-08-31
Last updated
2025-12-23

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

Conditions

Colorectal Cancer

Keywords

Virtual reality video training, colorectal surgery, self-efficacy

Brief summary

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.

Detailed 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.

Interventions

The patients who agreed to participate in the study will be asked to fill out a Patient Introduction Form by the researchers after obtaining permission from the experimental group with the Informed Consent Form the day before the surgery. On the 2nd day after laparoscopic colorectal surgery, virtual reality glasses will be worn by the patients and they will watch a 10-minute training video on the care of the patient after colorectal surgery. The training content will consist of topics such as dressing the surgical area, signs of infection in the surgical area (redness, swelling, discharge, color, temperature increase), pain management, unexpected situations (fever, nausea, abdominal pain, shivering, chan)

Sponsors

Ankara Yildirim Beyazıt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion 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

Design outcomes

Primary

MeasureTime frameDescription
Self-Efficacy Scale in Colorectal Cancer Surgeryone week after registration up to 3 monthsThis 16-question scale is scored using a Likert scale ranging from not at all sure to very sure (0-10). Questions include the ability to detect changes in the wound site (edema, redness, discharge, pain, discoloration, and increased temperature), timely medication use, dressing, seeking medical attention, regulating diet, detecting urinary changes, maintaining social relationships, and avoiding strenuous exercise. A higher score indicates an increase in self-efficacy.

Countries

Turkey (Türkiye)

Contacts

Primary ContactGÜLÇİÇEK TÜRKGENÇ
cicek.gungor153@gmail.com+90 507 164 4838

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026