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Can Virtual Reality Technology Improve the Patient Experience in Oocyte Retrieval?

Not Applicable
Recruiting
Conditions
Infertility, Female
Interventions
Device: Virtual reality technology
Registration Number
NCT05826938
Lead Sponsor
Peter Humaidan
Brief Summary

A non-pharmacological, non-blinded, randomized cohort study that will investigate the effect of Virtual Reality technology on the patient experience during oocyte retrieval.

The primary objective of the trial is to investigate the impact of Virtual Reality technology on the patient experience

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
82
Inclusion Criteria
  • Women undergoing oocyte retrieval
  • Understanding and speaking Danish
Exclusion Criteria
  • Previous participation in the trial
  • Acupuncture as pain relief during oocyte retrieval

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Virtual realityVirtual reality technologyThe intervention group receives stimuli in the form of Virtual Reality technology before and during oocyte retrieval. In addition, patients receive standard treatment
Primary Outcome Measures
NameTimeMethod
Questionnaires regarding impact on patient experience30-60 minutes

The impact of Virtual Reality technology on the patient experience during oocyte retrieval through questionnaires.

A visual analog scale (VAS) from 1-10 will be used for this measurement.

Secondary Outcome Measures
NameTimeMethod
Questionnaires reagarding the impact on the consumption of analgesic medication30-60 minutes

The effect of Virtual Reality technology on the consumption of analgesic medication.

A visual analog scale (VAS) from 1-10 will be used for this measurement.

Trial Locations

Locations (1)

Fertility Clinic Skive, Skive Regional Hospital

🇩🇰

Skive, Denmark

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