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Virtual Reality Distraction During Arteriovenous Fistula Puncture

The Effect of Virtual Reality Distraction on Pain and Anxiety During Arteriovenous Fistula Puncture Among Hemodialysis Patients: Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05399199
Enrollment
93
Registered
2022-06-01
Start date
2022-06-05
Completion date
2023-02-15
Last updated
2023-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemodialysis, Pain Management, Virtual Reality

Brief summary

The cannulation of arteriovenous fistula is a painful procedure in hemodialysis patients. Previous studies have shown the effectiveness of virtual reality in reducing pain during needle-related procedures

Detailed description

Patients undergoing hemodialysis experience anxiety and pain related to the insertion of hemodialysis needles, estimated 320 times in total per year. The pain experienced is mostly caused by needle insertion into a fistula. Pain control is one of the main nursing tasks. Pain relief leads to the acceptance of the procedure and ultimately enhances the patients' quality of life. The use of virtual reality to reduce pain and anxiety during the arteriovenous fistula cannulation procedure is based on the concept that the perception of pain can be controlled because an individual is able to process only a limited amount of information at once. As such, the use of virtual reality during painful procedures may serve as a distraction.

Interventions

PROCEDUREvirtual reality distraction

study group patients will view VR scene for 6 minutes before puncture .It involves a soothing nature experience and calming background music. Patients in intervention group will not able to see the puncture procedure due to the VR glasses.

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* patients who are under- going conventional hemodialysis three times a week * hemodialysis period of one month or more * having a healthy AVF access with good function * welling to participate in study

Exclusion criteria

* patients who have psychiatric diseases * panic disorder, anxiety disorder * dysfunctional fistula * vertigo, issues with sight, hearing, or perception * or use painkillers within three hours before hemodialysis

Design outcomes

Primary

MeasureTime frameDescription
change in patients pain scoreswill be measured at baseline and immediately after intervention (after 6 minutes of VR distraction)visual analogue scale which consists of a vertical line 100 mm long, one end of the line reads No pain and at the other is Unbearable pain
change in patients anxiety scoreswill be measured at baseline and immediately after intervention (after 6 minutes of VR distraction)STAI includes two subscales with 20 items each that assess state and trait anxiety .The State Anxiety Scale requires individuals to describe their feelings at a specific moment under specific circumstances, while the Trait Anxiety Scale requires them to describe the way they feel in general.

Secondary

MeasureTime frameDescription
change in patients respiratory ratewill be measured at baseline and immediately after intervention (after 6 minutes of VR distraction)checklist will be used to assess respiratory rate after puncture
change in patients systolic blood pressurewill be measured at baseline and immediately after intervention (after 6 minutes of VR distraction)checklist will be used to assess systolic blood pressure after puncture
change in patients satisfaction scorewill be measured at baseline and immediately after intervention (after 6 minutes of VR distraction). The patients will be asked to rate procedure satisfaction placing a mark on a 100-mm vertical visual analogue scale
change in patients Oxygen saturation (SpO2)will be measured at baseline and immediately after intervention (after 6 minutes of VR distraction)checklist will be used to assess Oxygen saturation after puncture
change in patients diastolic blood pressurewill be measured at baseline and immediately after intervention (after 6 minutes of VR distraction)checklist will be used to assess diastolic blood pressure after puncture
change in patients heart ratewill be measured at baseline and immediately after intervention (after 6 minutes of VR distraction)checklist will be used to assess heart rate after puncture

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026