The Effect of Virtual Reality Application on Anxiety and Patient Satisfaction During Intrauterine Insemination (IUI)

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-15

Study Completion Date

2024-09-30

Brief Summary

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This study will conduct as a randomized pretest-posttest study to examine the effect of virtual reality glasses (VRG) application during the IUI procedure on anxiety and patient satisfaction. The population of the research will consist of women who were treated with assisted reproductive techniques and underwent IUI at the infertility polyclinic of Ministry of Health Adana City Training and Research Hospital between May and December 2024 and who meet the research criteria. The research sample was calculated as a total of 90 people (at least 45 people in each group) using the power program. Data; Personal Information Form, Visual Assessment Scale (VAS), State Trait Anxiety Inventory (STAI) and Patient's Perception of Nursing Care Scale will be collected from women who agree to participate in the research. Virtual reality glasses will be applied to the intervention group.

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Detailed Description

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This study will conduct as a randomized pretest-posttest study to examine the effect of virtual reality glasses (VRG) application during the IUI procedure on anxiety and patient satisfaction. The population of the research will consist of women who were treated with assisted reproductive techniques and underwent IUI at the infertility polyclinic of Ministry of Health Adana City Training and Research Hospital between May and December 2024 and who meet the research criteria. The research sample was calculated as a total of 90 people (at least 45 people in each group) using the power program. Data; Personal Information Form, Visual Assessment Scale (VAS), State Trait Anxiety Inventory (STAI) and Patient's Perception of Nursing Care Scale will be collected from women who agree to participate in the research. These scales will be applied to both groups before and after Intrauterine Insemination (IUI).

Virtual reality glasses will be applied to the intervention group during intrauterine insemination (IUI).

Keywords: Virtual reality, anxiety, patient satisfaction, Intrauterine Insemination (IUI)

Conditions

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Virtual Reality Anxiety Patient Satisfaction Intrauterine Insemination (IUI)

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The sample will divide into intervention and control groups

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Virtual reality glasses to intervention group

Virtual reality glasses to intervention group, randomized pretest-posttest

Group Type EXPERIMENTAL

Virtual reality glasses to intervention group

Intervention Type DEVICE

experimental and control ,a randomized pretest-posttest study to examine

control

Non-intervention

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Virtual reality glasses to intervention group

experimental and control ,a randomized pretest-posttest study to examine

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* 18-45 age group
* Primary infertile,
* Able to speak and understand Turkish,
* Are cognitive, effective and have no problems preventing communication,
* Having no psychiatric problems,
* Not diagnosed with epilepsy (due to the possibility of virtual reality (VR) glasses triggering epileptic seizures),
* Women who volunteer to participate in the study will be recruited.