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

NCT07078656 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2025-12-23

No results posted yet for this study

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.

Conditions

Interventions

BEHAVIORAL

Postoperative management

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 & Collaborators

  • Ankara Yildirim Beyazıt University

    lead OTHER

Principal Investigators

  • Tuba Yılmazer, Ass. Prof. · Ankara Yildirim Beyazıt University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-30
Primary Completion
2026-07-31
Completion
2026-08-31

Countries

  • Turkey (Türkiye)

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07078656 on ClinicalTrials.gov