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Effect of Two Different Methods on Pain and Anxiety

N

Necmettin Erbakan University

Status

Completed

Conditions

Pain

Treatments

Device: Stress Ball
Device: Virtual Reality Glasses

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study is to determine the effect of virtual reality glasses and ball squeezing method used during peripheral intravenous catheter placement on pain and anxiety.The hypotheses of this research are that virtual reality glasses and a stress ball reduces pain and anxiety.

Full description

This study was designed as a pretest-posttest regular parallel group, randomized controlled experimental. The research will be carried out in the general surgery clinic of Necmettin Erbakan University Meram Medical Faculty Hospital. Patients will be randomly assigned to three groups: ball squeezing (37), virtual reality glasses (37) and control group (37). For Virtual Reality Glasses Group: The video containing the nature walk will be watched by virtual reality. 3 minutes after the individual starts watching the video, the IV catheter insertion attempt will be performed while continuing to watch the video. For Ball Squeezing Group: Patients will be given a ball and instructed to tighten and loosen with their free hand during intravenöz catheter placement. The intravenöz catheter insertion attempt will be made while the patient continues to squeeze the ball. For Control Group: No application will be made during intravenous catheter placement in the control group.The primary outcome of this study was to determine the patients' pain scores during the peripheral venous cannula insertion process.The secondary outcomes of the study were to determine the patients' anxiety levels.

Enrollment

111 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Admission to the General Surgery clinic.
  • No verbal, perceptual and visual communication problems,
  • Being between 18 - 65 years old,
  • Being literate,
  • Volunteer to participate in the research,
  • Not using drugs that will create a chronic analgesic effect,
  • Absence of chronic or acute pain,
  • No intervention in the last month in the vein where an IV catheter was placed.
  • The absence of scar tissue and infection in the areas to be used for IV catheter placement,
  • It was determined as not having a disease (such as neuropathy) that would cause problems in feeling pain.

Exclusion criteria

  • The individual's desire to leave the study,
  • Inability to perform the ball squeezing motion,
  • Feeling unwell during IV catheter placement (such as dizziness, palpitations),
  • During use of VR, the patient experiences symptoms such as nausea and dizziness,
  • Using sedatives or alcohol,

Termination criteria

• Failure of PIV catheter placement,

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

111 participants in 3 patient groups

Virtual Reality Glasses Group
Experimental group
Description:
* "Volunteer Information and Approval Form" will be filled. * Physician request, the name and surname of the individual will be checked. * Patient Information Form and State Anxiety Scale will be filled. * The video containing the nature walk will be watched by virtual reality. 3 minutes after the individual starts watching the video, the IV catheter insertion attempt will be performed while continuing to watch the video. * Visual Pain Scale and State Anxiety Scale will be filled within one minute after intravenous catheter placement is completed.
Treatment:
Device: Virtual Reality Glasses
Ball Squeezing Group
Experimental group
Description:
* "Volunteer Information and Approval Form" will be filled. * Physician request, the name and surname of the individual will be checked. * Patient Information Form and State Anxiety Scale will be filled. * Patients will be given a ball and instructed to tighten and loosen with their free hand during IVC placement. The IV catheter insertion attempt will be made while the patient continues to squeeze the ball. * Visual Pain Scale and State Anxiety Scale will be filled within one minute after intravenous catheter placement is completed.
Treatment:
Device: Stress Ball
Control Group:
No Intervention group
Description:
* "Volunteer Information and Approval Form" will be filled. * Physician request, the name and surname of the individual will be checked. * Patient Information Form and State Anxiety Scale will be filled. * An intravenous catheter will be placed. * Visual Pain Scale and State Anxiety Scale will be filled within one minute after intravenous catheter placement is completed.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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