Status:

COMPLETED

The Effect of Different Images Watched With Virtual Reality During Phlebotomy

Lead Sponsor:

Zonguldak Bulent Ecevit University

Conditions:

Pain Management

Anxiety Management

Eligibility:

All Genders

18-35 years

Phase:

NA

Brief Summary

Aim: The purpose of this study was to investigate the effect of watching a cold environment image via virtual reality on pain and anxiety related to phlebotomy procedure in volunteer blood donors. Me...

Eligibility Criteria

Inclusion

  • Being in accordance with time and place
  • Being aged between 18 and 35 years
  • Being able to evaluate the visual analog scale correctly
  • Participating voluntarily in the research.
  • Being willing to donate blood
  • Donating blood for the first time
  • Have a body mass index within normal limits (18.5-24.9 kg/m2)
  • Have no vision or hearing problems
  • Have no disease that may affect pain perception
  • Have no vertigo, heart or lung disease
  • Have no signs of infection, dermatitis, phlebitis, scar tissue or incision in the area where invasive intervention will be performed
  • Have no psychiatric disease
  • Being able to accurately assess the state and trait anxiety inventory with the VAS
  • Have an average pressure pain threshold value of 8-16 Lb obtained from three measurements taken at 5-second intervals from the elbow region of the left upper extremity where no intervention was performed
  • Have no vertigo, heart or lung disease
  • Have no signs of infection, dermatitis, phlebitis, scar tissue or incision in the area where invasive intervention will be performed
  • Have no psychiatric disease
  • Being able to accurately assess the state and trait anxiety inventory with the VAS
  • Have an average pressure pain threshold value of 8-16 pounds (Lb) obtained from three measurements taken at 5-second intervals from the elbow region of the left upper extremity where no intervention was performed

Exclusion

  • Not participating voluntarily in the research
  • Not fitting the inclusion criteria of the research
  • Having a vision or hearing problem
  • Failure of phlebotomy at the first attempt
  • Development of syncope after phlebotomy

Key Trial Info

Start Date :

April 18 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 10 2020

Estimated Enrollment :

120 Patients enrolled

Trial Details

Trial ID

NCT06487520

Start Date

April 18 2019

End Date

July 10 2020

Last Update

July 5 2024

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Zonguldak Bulent Ecevit University

Zonguldak, Turkey (Türkiye)