Actively Recruiting
Perioperative Virtual Reality Intervention for Pain and Anxiety During Vasectomies
Led by University of Manitoba · Updated on 2026-05-05
90
Participants Needed
1
Research Sites
56 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if a virtual reality (VR) program (TRIPP) can reduce pain, anxiety, and distress in adult men (aged 18+) undergoing a vasectomy under local anesthesia. The main questions it aims to answer are: * Does using VR during a vasectomy lower patients' pain during the procedure compared to standard care? * Does VR reduce anxiety and distress compared to standard care? * Are patients more satisfied with their experience when using VR compared to standard care? Researchers will compare two groups: * VR group: Patients will use a VR headset with a guided meditation program (TRIPP) during their vasectomy. * Control group: Patients will receive standard care (no VR). Participants will: * Be randomly assigned to either the VR group or control group. * Complete brief questionnaires before, during, and after the procedure (about 15-20 minutes each time). * (VR group only) Use a VR headset during the procedure and provide optional feedback about the experience. Why is this important? Vasectomies are typically done with local anesthesia (pain relief), but many patients still feel anxiety or discomfort. VR may help distract and relax patients, improving their experience. This study will help health professionals understand if VR could be a useful option for future patients.
CONDITIONS
Official Title
Perioperative Virtual Reality Intervention for Pain and Anxiety During Vasectomies
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Can speak and read English
- Have elected for a vasectomy
- Are scheduled to undergo their vasectomy under local anesthesia at the Men's Health Clinic
You will not qualify if you...
- Not competent to provide informed consent (e.g., due to cognitive impairment)
- Unable to participate in a VR intervention (e.g., due to visual or auditory impairment)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Manitoba Men's Health Clinic
Winnipeg, Manitoba, Canada, R3P 2S8
Actively Recruiting
Research Team
R
Renée El-Gabalawy, MA, PhD, C.Psych.
CONTACT
A
Ahmed M Zalam, B.Sc.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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