Clinical trial · Interventional
Effect of Video Training on Patients' Self-Efficacy After Colorectal Surgery
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Colorectal Cancer | Malignant Colorectal Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Postoperative management | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Virtual Reality Glasses
- description
- 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.
- interventionNames
- Behavioral: Postoperative management
- type
- NO_INTERVENTION
- label
- Control
- description
- 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 outcomes (1)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available