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New treatment option for Urologic Diseases
Official title VIrtual Reality Induced Pain and anxiEty Relief in Outpatient UROlogical Procedures
ClinicalTrials.gov ID: NCT07338292
What this study is testing
- What it's testing
- Though the efficacy of VRH is documented in various outpatient urological procedures and has provided promising preliminary information in prostate biopsy, its systematic use in urology remains poorly studied. Considering the potential of invasive urological procedures to induce significant patient discomfort, the application of innovative immersive approaches, such as those offered by medical devices, could lead to an overall clinical benefit.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 99
You may be able to join if
- Male/female with age ≥ 18 years
- Patient who are undergoing one of the interventions mentioned in the study for the first time;
- Eligibility for minimally invasive ambulatory urological procedures, possibly requiring vascular access (circumcision, prostate biopsy, flexible...
- Ability to understand instructions and complete study questionnaires;
- Signed informed consent.
You likely can't join if
- Absolute contraindications to the planned urological procedure (e.g., active urinary tract infection, anatomical urethral abnormalities);
- Recent urological manipulations (e.g., urethral dilation, bladder biopsy, insertion or removal of a double-J stent);
- Medical contraindications to the use of virtual reality, including uncontrolled photosensitive epilepsy and relevant neurological, ophthalmologic, or...
- Presence of severe psychiatric disorders or major cardiovascular diseases that may interfere with study participation;
- Previous adverse reactions to virtual reality exposure;
- Use of analgesic medications within 24 hours prior to the procedure;
See the full eligibility criteria
- Male/female with age ≥ 18 years
- Patient who are undergoing one of the interventions mentioned in the study for the first time;
- Eligibility for minimally invasive ambulatory urological procedures, possibly requiring vascular access (circumcision, prostate biopsy, flexible cystoscopy);
- Ability to understand instructions and complete study questionnaires;
- Signed informed consent.
- Absolute contraindications to the planned urological procedure (e.g., active urinary tract infection, anatomical urethral abnormalities);
- Recent urological manipulations (e.g., urethral dilation, bladder biopsy, insertion or removal of a double-J stent);
- Medical contraindications to the use of virtual reality, including uncontrolled photosensitive epilepsy and relevant neurological, ophthalmologic, or otolaryngologic disorders;
- Presence of severe psychiatric disorders or major cardiovascular diseases that may interfere with study participation;
- Previous adverse reactions to virtual reality exposure;
- Use of analgesic medications within 24 hours prior to the procedure;
- Use of drugs that may alter consciousness or impair the ability to complete psychological assessments;
- Severe communication disabilities or significant hearing impairment that would prevent completion of questionnaires.
The study team makes the final eligibility decision.
Where it's taking place
- Padova, Italy
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 99 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Padova, Italy. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.