Intramuscular Benzathine Penicillin Injection Procedure

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

COMPLETED

Clinical Phase

NA

Total Enrollment

91 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-17

Study Completion Date

2018-04-30

Brief Summary

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The aim of this study was the determination of the effect of applying VR and DC distraction methods on patients' pain and satisfaction levels during IM benzathine penicillin injection.

The research hypothesis:

1. Are Virtual Reality and Distraction Card effective in reducing pain due to injection of IM benzathine penicillin?
2. Does the use of Virtual Reality and Distraction Card during the injection process of IM benzathine penicillin have an effect on patient satisfaction?

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Detailed Description

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Conditions

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Injection Site Discomfort

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Virtual Reality

Group Type EXPERIMENTAL

Intramuscular Injection

Intervention Type OTHER

Intramuscular Benzathine Penicillin Injection Procedure

Distraction Card

Group Type EXPERIMENTAL

Intramuscular Injection

Intervention Type OTHER

Intramuscular Benzathine Penicillin Injection Procedure

Control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Intramuscular Injection

Intramuscular Benzathine Penicillin Injection Procedure

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* agree to participate in the research,
* being over the age of 18,
* being native speaker,
* not having vision and hearing problems,
* being prescribed benzathine penicillin with a dose of 1.200.000 IU,
* being experienced of IM injection,
* not having IM injection for the last 1 month

Exclusion Criteria

* volunteers who have scar, incision, lipodystrophy, abscess, necrosis, hematoma, ecchymosis, infection, pain and paralysis at the VG site
* volunteers are excluded if the injection process cannot be performed at one time

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No