NCT05373797

Brief Summary

The study was planned as a prospective randomized controlled study and was carried out in the Training and Research Hospital burn unit outpatient clinic between 05.7.2021-1.04.2022. The population of the study consisted of the parents of children aged 5-10 years who applied to the burn unit polyclinic for dressing between the dates of the study. A total of 52 people were included in the research group. Data were collected by using the "Survey Form" consisting of 10 questions, "Newcastle Nursing Satisfaction Scale" and "Beck Anxiety Scale".

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started May 2021

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 7, 2021

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 4, 2022

Completed
23 days until next milestone

First Submitted

Initial submission to the registry

April 27, 2022

Completed
7 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 4, 2022

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 13, 2022

Completed
Last Updated

July 15, 2022

Status Verified

May 1, 2022

Enrollment Period

11 months

First QC Date

April 27, 2022

Last Update Submit

July 13, 2022

Conditions

Outcome Measures

Primary Outcomes (1)

  • The Effect of Virtual Reality Glasses Used During Burn Dressing in Children on Parents' Satisfaction Level and Anxiety

    Using virtual reality glasses lowers parental anxiety

    May 2022- October2022

Study Arms (1)

experimental and control group

experimental: 26 control group:26

Behavioral: Procedures performed on the experimental and control groups

Interventions

Intervention Group:26 Control Group (n=26):

Also known as: experimental and control group
experimental and control group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

In order to determine the number of samples, power analysis was performed using the G\*power program. The effect size coefficient was calculated by using the Newcastle satisfaction scale averages in source 1 (thesis), and the effect size = 0.76, and it was decided to recruit at least 26 people in each group in order to obtain 80% power at the ɑ=0.05 level, a total of 52 people in the two groups.

You may qualify if:

  • parents
  • read and write,
  • understand Turkish,

You may not qualify if:

  • under the age of 18
  • do not want to participate in the study
  • cannot be pregnant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Samsun Health Directorate

Samsun, İlkadım, Turkey (Türkiye)

Location

19May University

Samsun, 34100, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Control Groups

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Officials

  • Esra TURAL, PhD

    omu

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

April 27, 2022

First Posted

May 13, 2022

Study Start

May 7, 2021

Primary Completion

April 4, 2022

Study Completion

May 4, 2022

Last Updated

July 15, 2022

Record last verified: 2022-05

Locations