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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04420559
Other study ID # 18/18
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 17, 2018
Est. completion date April 30, 2018

Study information

Verified date April 2024
Source Saglik Bilimleri Universitesi
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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?


Recruitment information / eligibility

Status Completed
Enrollment 91
Est. completion date April 30, 2018
Est. primary completion date April 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Intramuscular Injection
Intramuscular Benzathine Penicillin Injection Procedure

Locations

Country Name City State
Turkey Gulhane Training and Research Hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Saglik Bilimleri Universitesi

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analog Scale for pain measurement (Minimum score: 0 ; Maximum score:10) Higher scores mean a worse outcome 4 months
Secondary Visual Analog Scale for satisfaction measurement (Minimum score: 0 ; Maximum score:10) (Minimum score: 0 ; Maximum score:10) Higher scores mean a better outcome 4 months
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