Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07265960

Effect of Virtual Reality and Stress Ball Interventions on Procedure-Related Fear, Pain, Anxiety, and Patient Satisfaction in Patients Undergoing Ureterorenoscopy

Led by Tarsus University · Updated on 2026-02-05

90

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of virtual reality and stress ball interventions on fear, anxiety, pain, and patient satisfaction in adults undergoing ureterorenoscopy. This prospective, randomized controlled clinical trial involves 90 patients divided into three groups to study procedure-related psychological and physical responses. The study uses validated tools like the State Anxiety Inventory, Procedure-Related Fear Scale, Visual Analog Scale, and Newcastle Satisfaction with Nursing Care Scale to measure outcomes. Participants in the virtual reality group will watch nature scenes with relaxing music through a VR headset during their clinic visit. The stress ball group will use a stress ball by squeezing it repeatedly until they leave the clinic. The control group will receive routine pre-procedure care without additional interventions. Each intervention is applied in the clinic before and during the ureterorenoscopy procedure. All participants will complete questionnaires assessing anxiety and fear before the procedure and anxiety, pain, and satisfaction after the procedure while resting in bed. Researchers will analyze the data using statistical tests to compare the effects of the interventions. The study aims to understand how these non-drug methods influence patient experience during ureterorenoscopy, with follow-up assessments planned for up to six months.

CONDITIONS

Brief Title

Effects of Virtual Reality and Stress Ball on Fear, Pain, Anxiety, and Satisfaction in Ureterorenoscopy Patients

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 years or older
  • Scheduled for ureteroscopy (URS)
  • Fully conscious, oriented, and cooperative
  • Provided written informed consent to participate in the study
  • Able to speak and understand Turkish
  • Without visual or hearing impairments
  • No prior experience with virtual reality (VR)
  • Without any mental health disorders
Not Eligible

You will not qualify if you...

  • Those who do not wish to participate or who wish to withdraw from the study
  • Patients with chronic pain

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Single day of procedure

Participants undergo ureterorenoscopy and receive one of the following interventions in the clinic: virtual reality viewing of nature scenes with relaxing music, use of a stress ball, or routine pre-procedure care without additional intervention.

1 procedure day visit (in-person)

Follow-up

Duration - Single post-procedure assessment

After the procedure, participants complete assessments of anxiety, pain, fear, and satisfaction while in the clinic bed.

1 post-procedure visit (in-person)

Trial Site Locations

Total: 1 location

1

Tarsus University

Mersin, Tarsus, Turkey (Türkiye), 33400

Actively Recruiting

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Research Team

G

Gamze Bozkul

Y

Yurdagül Günaydın

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

3

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