Virtual reality video may help patients recover confidence after colorectal surgery
NCT ID NCT07078656
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether watching a 10-minute training video through virtual reality glasses on the second day after colorectal surgery can improve patients' self-efficacy—their confidence in managing their own recovery. 66 adults aged 18–65 who had laparoscopic surgery will be split into two groups: one watches the video, the other does not. Ten days after discharge, both groups fill out a survey to measure self-efficacy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- virtual reality video training
- What this could lead to
- If it works, this could provide a simple, low-cost way to help patients feel more capable and confident after colorectal surgery.
- What could go wrong
- This is a small, early-stage study with only 66 participants. The training is brief (10 minutes) and may not have a lasting impact on self-efficacy or recovery outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 66 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Etlik City Hospital
Ankara, Turkey (Türkiye)
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