Status:

COMPLETED

The Effect of Virtual Reality on Anxiety During Intrauterine Device Insertion

Lead Sponsor:

Kırklareli University

Conditions:

Intrauterine Device

Eligibility:

FEMALE

18-85 years

Phase:

NA

Brief Summary

This study was planned to determine whether the use of virtual reality glasses during intrauterine device insertion has an effect on the anxiety level of women.

Detailed Description

Intrauterine device (IUD), which is one of the effective contraceptive methods in our country, is one of the known and frequently used methods. According to TDHS 2018 data, it was reported that 35% of...

Eligibility Criteria

Inclusion

  • -Volunteering to participate in the research
  • Answering questionnaire and scale forms completely
  • Read and understand Turkish
  • 18 years of age or older
  • STAI score of 35 and above
  • Not being pregnant,
  • No complaints of acute pelvic pain,
  • No damage or leysone in the perineum that may cause pain during examination,
  • Not using a pharmacological agent or method with analgesic or anxiolytic effect 24 hours before the application,
  • No vaginismus problem,
  • Absence of a history of sexual abuse,
  • Not having any physical or mental problems that may prevent communication.

Exclusion

  • -Not volunteering to participate in the research,
  • Incomplete responses to questionnaires and scale forms
  • Not understanding Turkish,
  • Under 18 years of age
  • Do not score less than 35 points on the STAI,
  • Don't be pregnant,
  • Complaint of acute pelvic pain,
  • Any damage or leysone in the perineum that may cause pain during examination,
  • Having used a pharmacological agent or method with analgesic or anxiolytic effect 24 hours before the application,
  • Having a vaginismus problem,
  • Previous history of sexual abuse,
  • Having any physical or mental problem that prevents communication.

Key Trial Info

Start Date :

May 1 2024

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 26 2024

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT06179095

Start Date

May 1 2024

End Date

September 26 2024

Last Update

October 8 2024

Active Locations (1)

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Page 1 of 1 (1 locations)

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1.Murat State Hospital

Edirne, Turkey (Türkiye)