NCT07493499 Virtual Reality for Postoperative Recovery After Major Abdominal Surgery
| NCT ID | NCT07493499 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Alexandria University |
| Condition | Abdominal Surgery |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2026-03-28 |
| Primary Completion | 2026-04 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2026-03-28 with a primary completion date of 2026-04.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Major abdominal surgery often leads to significant postoperative pain, anxiety, and prolonged hospital stays, which can delay overall recovery. This study aims to evaluate the effectiveness of immersive Virtual Reality (VR) as a non-pharmacological intervention to enhance the quality of recovery and reduce the length of hospital stay. Patients in the intervention group will engage in standardized VR sessions featuring guided relaxation and mindfulness-based stress reduction, starting from the evening before surgery through the third postoperative day. The study compares this VR-enhanced protocol against standard perioperative care within an Enhanced Recovery After Surgery (ERAS) framework. The findings are expected to determine if VR can serve as a feasible and effective tool to improve clinical outcomes and patient well-being in surgical wards.
Eligibility Criteria
Inclusion Criteria: * Adult patients aged 18 to 60 years. * Scheduled for elective major abdominal surgery (e.g., colorectal, gastric, or hepatobiliary procedures). * Physical and cognitive ability to provide informed consent. * Ability to use and interact with Virtual Reality (VR) equipment (head-mounted display). * Followed the standardized Enhanced Recovery After Surgery (ERAS) protocol at the hospital. Exclusion Criteria: \- Patients with a history of epilepsy or photosensitive seizures. * Significant cognitive impairment or diagnosed psychiatric disorders that may interfere with study participation. * Severe visual or auditory impairments that prevent effective interaction with VR content. * Patients with pre-existing motion sickness or severe vertigo. * Presence of open wounds or infections in the head or face area that prevent wearing the VR headset.
Contact & Investigator
Mohamed Fakhry Ahmed Salem Dr. Mohamed Fakhry Ahmed Salem, PhD
✉ Mohamed.Fakhry@alexu.edu.eg📞 +201286038014
Frequently Asked Questions
Who can join the NCT07493499 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 60 Years, studying Abdominal Surgery. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07493499 currently recruiting?
Yes, NCT07493499 is actively recruiting participants. Contact the research team at Mohamed.Fakhry@alexu.edu.eg for enrollment information.
Where is the NCT07493499 trial being conducted?
This trial is being conducted at Alexandria, Egypt.
Who is sponsoring the NCT07493499 clinical trial?
NCT07493499 is sponsored by Alexandria University. The trial plans to enroll 60 participants.