Effect of Video Training on Patients' Self-Efficacy After Colorectal Surgery
NCT ID: NCT07078656
Last Updated: 2025-12-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
66 participants
INTERVENTIONAL
2026-06-30
2026-08-31
Brief Summary
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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.
Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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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.
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)
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.
No interventions assigned to this group
Interventions
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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)
Eligibility Criteria
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Inclusion Criteria
* 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 are hemodynamically unstable
* with an ASA score of IV
* with neurological or psychological problems
* Emergency and unplanned cases
18 Years
65 Years
ALL
No
Sponsors
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Ankara Yildirim Beyazıt University
OTHER
Responsible Party
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Gülçiçek Güngör
Graduate Student
Principal Investigators
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Tuba Yılmazer, Ass. Prof.
Role: STUDY_DIRECTOR
Ankara Yildirim Beyazıt University
Locations
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Etlik City Hospital
Ankara, , Turkey (Türkiye)
Countries
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Central Contacts
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Other Identifiers
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AnkaraYBU-SBF-GG-01
Identifier Type: -
Identifier Source: org_study_id