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Clinical Trials in Turkey / NCT07078656
Starting soon Not applicable

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

NCT07078656 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06
Last updated
2025-12-23

Condition(s) studied

Colorectal Cancer

Investigational drug(s) / intervention(s)

Postoperative management

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)

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Etlik City Hospital Ankara Turkey (Türkiye)

More Ankara Yildirim Beyazıt University trials in Turkey

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07078656 on ClinicalTrials.gov ↗ ← All trials in Turkey