NCT06638164

Brief Summary

The aim of this study; To measure the effectiveness of isolation training given to caregivers using different training methods. As a result of this measurement, the more effective method will be used routinely. In this way, it is aimed to create more conscious patients and caregivers. In this study, two different training methods will be used and the methods will be compared. Methods; It is divided into two as the experimental group, the training to be given with virtual glasses, and the training given with the control group, as the standard training booklet. With virtual glasses, patients will be trained in an interactive way with three-dimensional video, and they will be able to see and then apply them. The training to be given with the training booklet includes standard procedure and 2D visual and verbal expression. Based on this information, this study aims to evaluate the effectiveness of the Isolation Training Given to the Caregivers of Isolated Sick Individuals with Different Methods.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

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

August 1, 2022

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2022

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2022

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

November 22, 2022

Completed
1.9 years until next milestone

First Posted

Study publicly available on registry

October 15, 2024

Completed
Last Updated

October 15, 2024

Status Verified

October 1, 2024

Enrollment Period

1 month

First QC Date

November 22, 2022

Last Update Submit

October 9, 2024

Conditions

Keywords

IsolationVirtual Reality GlassesAchievementKnowledgeSatisfaction

Outcome Measures

Primary Outcomes (2)

  • Achievement levels

    The caregivers of the isolated individuals were informed about the isolation precautions checklist.It was created in line with the literature to determine the knowledge levels regarding the ability to apply Isolation Precautions.It is a checklist consisting of 20 items that evaluates isolation precautions and wearing protective equipment, created by researchers in line with the literature. The lowest score that can be obtained from the checklist is "0", and the highest score is "100".

    2 Months

  • Knowledge levels

    The caregivers of the isolated individuals were informed about the knowledge exam.It is a survey consisting of 20 questions covering isolation precautions created by researchers in line with the literature.The lowest score that can be obtained from the knowledge exam is "0", and the highest score is "100".

    2 Month

Secondary Outcomes (1)

  • Satisfaction levels

    2 Months

Study Arms (2)

Control Group

EXPERIMENTAL

No attempt was made to increase knowledge, skills and satisfaction. Standard procedure (oral explanation) was applied.

Other: Control

Virtual Reality Glasses Group(Experiment)

EXPERIMENTAL

In order to increase knowledge, skills and satisfaction, isolation training was given with virtual reality glasses.

Other: Virtual reality glasses

Interventions

ControlOTHER

No attempt was made to increase knowledge, skills and satisfaction. Standard procedure (oral explanation) was applied.

Control Group

In order to increase knowledge, skills and satisfaction, isolation training was given with virtual reality glasses.

Virtual Reality Glasses Group(Experiment)

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • The caregiver;
  • The patient has a hospital infection that requires isolation,
  • The patient has immune deficiency and the implementation of isolation measures,
  • Not visually impaired
  • Being able to read and write
  • Written and verbal consent is obtained for participation in the study.

You may not qualify if:

  • The caregiver;
  • The patient does not have a hospital infection that needs to be isolated,
  • The patient has immune deficiency and isolation measures are not applied,
  • Having a visually impaired being illiterate
  • Written and verbal consent is not obtained for participation in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Beykent University

Istanbul, 34500, Turkey (Türkiye)

Location

Related Publications (4)

  • Butt, A. L., Kardong-Edgren, S., & Ellertson, A. (2018). Using game-based virtual reality with haptics for skill acquisition. Clinical Simulation in Nursing, 16, 25-32.

    RESULT
  • Onturk ZK, Ugur E, Kocatepe V, Ates E, Ocaktan N, Unver V, Karabacak U. Use of simulation from high fidelity to low fidelity in teaching of safe-medication practices. J Pak Med Assoc. 2019 Feb;69(2):195-200.

  • Kolbe L, Jaywant A, Gupta A, Vanderlind WM, Jabbour G. Use of virtual reality in the inpatient rehabilitation of COVID-19 patients. Gen Hosp Psychiatry. 2021 Jul-Aug;71:76-81. doi: 10.1016/j.genhosppsych.2021.04.008. Epub 2021 Apr 29.

  • Kizil H, Altintop I. Evaluation of the effectiveness of isolation training given to the caregivers of patients in isolation with different methods: a randomized controlled study. BMC Nurs. 2025 Sep 29;24(1):1219. doi: 10.1186/s12912-025-03662-0.

MeSH Terms

Conditions

Personal Satisfaction

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Hamiyet Kızıl, PhD RN

    Beykent University

    PRINCIPAL INVESTIGATOR
  • Hamiyet Kızıl

    Beykent University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD RN Assistant Professor Hamiyet KIZIL

Study Record Dates

First Submitted

November 22, 2022

First Posted

October 15, 2024

Study Start

August 1, 2022

Primary Completion

September 1, 2022

Study Completion

October 1, 2022

Last Updated

October 15, 2024

Record last verified: 2024-10

Data Sharing

IPD Sharing
Will not share

Locations