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NCT07078656Not yet recruiting

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

Source: ClinicalTrials.gov · Last updated 23 Dec 2025

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
66 (estimated)
First submitted
13 Jul 2025
Start date
1 Jun 2026
Primary completion date
31 Jul 2026
Lead sponsor
Ankara Yildirim Beyazıt University
NCT number
NCT07078656

What you commit to

  • Study type: Interventional
  • Planned participants: 66
  • From 1 Jun 2026 to the primary completion date, 31 Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • who have not undergone laparoscopic surgery

Other

  • who are hemodynamically unstable
  • with an ASA score of IV
  • with neurological or psychological problems
  • Emergency and unplanned cases

Criteria the registry did not label

  • 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

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Etlik City Hospital
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.