The Effect of Virtual Reality Glasses and Stress Balls on Pain and Vital Findings During Transrectal Prostate Biopsy: A Randomized Controlled Trial.
Hasan Genç, Medet Korkmaz, Abdullah Akkurt
https://pubmed.ncbi.nlm.nih.gov/35397973/Actively Recruiting
Led by Tarsus University · Updated on 2026-06-09
90
Participants Needed
1
Research Sites
30 weeks
Total Duration
This research aims to evaluate the effects of virtual reality and stress ball interventions on fear, anxiety, pain, and patient satisfaction in adults undergoing ureterorenoscopy. It is a prospective, randomized controlled clinical trial including 90 patients divided into three groups to compare these interventions impact on procedure-related stress and satisfaction. Participants in the virtual reality group will use a VR headset showing nature scenes with relaxing music adjusted to their preference while lying in a supine position. The stress ball group will be instructed to squeeze a stress ball repeatedly until they leave the clinic. The control group will receive routine pre-procedure care as usual. Interventions occur during the clinic visit before the ureterorenoscopy procedure. Before the procedure, all patients will complete questionnaires on demographics, anxiety, and fear. After the procedure, anxiety, pain levels, and satisfaction with nursing care will be assessed using validated scales. Data analysis will include statistical tests to compare the groups. The study will monitor outcomes over six months, with participation spanning the procedure day and follow-up assessments.
CONDITIONS
Effects of Virtual Reality and Stress Ball on Fear, Pain, Anxiety, and Satisfaction in Ureterorenoscopy Patients
G
Gamze Bozkul
Y
Yurdagül Günaydın
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Tarsus University
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of the ureterorenoscopy procedure
Participants will be randomly assigned to one of three groups: virtual reality, stress ball, or routine care. The virtual reality group will use a VR headset to view nature scenes with relaxing music before the procedure. The stress ball group will use a stress ball by squeezing it repeatedly until leaving the clinic. The control group will receive standard pre-procedure care.
1 visit (in-person)
Duration - 6 months
After the procedure, participants will complete questionnaires on anxiety, pain, and satisfaction while resting in bed. Researchers will monitor outcomes over six months using these assessments.
Regular assessments during follow-up period
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
3
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Hasan Genç, Medet Korkmaz, Abdullah Akkurt
https://pubmed.ncbi.nlm.nih.gov/35397973/Nurten Seyis Sibal, Ibrahim Sibal, Hamit Zafer Aksoy...
https://pubmed.ncbi.nlm.nih.gov/40780518/Tarsus University
Lead Sponsor