THE EFFECT OF VIRTUAL REALITY APPLICATION ON PAIN, ANXIETY, AND COMFORT DURING CURETTAGE/DILATATION

NCT ID: NCT06403579

Last Updated: 2024-05-08

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

ENROLLING_BY_INVITATION

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-01

Study Completion Date

2025-05-01

Brief Summary

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The problems experienced by women at the stage of deciding to have a miscarriage, during and after miscarriage differ and their anxiety levels vary. It was determined that women experienced fear, thinking that they would sin, guilt, regret and indecision at the stage of deciding to abort. methods are used to relieve the pain and anxiety caused by interventional procedures in patients in direct proportion to the development of technology. Virtual reality (VR), one of these methods, is an innovative, up-to-date and unique application, combining reality and imagination with fictional technology.There is no study in the literature on the application of SG during curettage/dilatation procedure. This study was conducted to determine the effect of SG application on pain anxiety and comfort during curettage/dilatation procedure.

Detailed Description

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Conditions

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Bleeding;Post D&C PAIN, ANXIETY, AND COMFORT

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

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virtual reality application

Experimental: virtual reality application virtual reality goggles will be implemented.

Group Type EXPERIMENTAL

virtula reality goggles

Intervention Type DEVICE

no intervention

control

No Intervention: control group no intervention will be made

Group Type SHAM_COMPARATOR

virtula reality goggles

Intervention Type DEVICE

no intervention

Interventions

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virtula reality goggles

no intervention

Intervention Type DEVICE

Other Intervention Names

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control

Eligibility Criteria

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Inclusion Criteria

* 15-49 years old,
* Termination ordered,
* Can speak and understand Turkish,

Exclusion Criteria

* \- Cognitive, effective and without any problem preventing communication,
* No psychiatric problems,
* Diagnosed with epilepsy (due to the risk that SG glasses may trigger epileptic seizures),
* Women who volunteer to participate in the study will be recruited.
Minimum Eligible Age

15 Years

Maximum Eligible Age

49 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Cukurova University

OTHER

Sponsor Role lead

Responsible Party

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seda karaçay yıkar

Assistant professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Seda Karaçay Yıkar

Adana, Sarıcam, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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142-16

Identifier Type: -

Identifier Source: org_study_id

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