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

Sponsor
Ankara Yildirim Beyazıt University
Study ID
NCT07078656
Status
Not Yet Recruiting

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Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • Postoperative management — BEHAVIORAL
    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)

Study Details

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.

Key Dates

First listed
Jul 22, 2025
Start date
Jun 30, 2026
Status verified
Dec 2025
Primary completion
Jul 31, 2026
Completion
Aug 31, 2026

Study Design

Enrollment
66 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: Virtual Reality Glasses
    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.
  • No Intervention: Control
    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.

Primary Outcome Measure

Self-Efficacy Scale in Colorectal Cancer Surgery [ Time Frame: one week after registration up to 3 months ]

Central Contacts

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