- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05248542
The Effects of Virtual Reality/ Augmented Reality Usage on Oral Care Knowledge in Nursing Students
9. februar 2022 opdateret af: Kaohsiung Medical University Chung-Ho Memorial Hospital
The aim of this study was to investigate the effects of virtual reality usage on oral care knowledge in nursing students.
The participants were randomly assigned to virtual-reality experimental and control groups.
The students in experimental group received a 30 minutes virtual reality (VR) training for elderly oral health care at the second week and the fourth week after the first time survey.
All students self-administrated questionnaire three times at first date of consent form signed, immediately after each of the intervention for period of two weeks.
Linear regression in generalized estimating equations (GEE) compare the differences between both groups.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
A total of 50 first-year to third-year undergraduate nursing students were included from the Department of Nursing, Kaohsiung Medical University, Taiwan.
The students were randomly assigned divided at random into two groups, control (n = 25) and experimental (n = 25).
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
50
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
-
Kaohsiung, Taiwan
- Kaohsiung Medical University
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 25 år (Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- undergraduate freshman, sophomore, and junior nursing students
- those volunteered to participate in this study
Exclusion Criteria:
- students with known negative effects of using VR devices, such as nausea, vomiting, etc.
- those under 20 years of age who had not obtained the consent of a legal representative to participate in this study.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: Virtual Reality group
Each participant in the experimental group received a 30 minutes of individualized VR-based simulation education in a dedicated oral skills training room.
|
Virtual Reality Usage on Oral Care Knowledge about independent older adults
|
Ingen indgriben: Control group
The control group only received repeated questionnaires and did not receive any education about geriatric oral hygiene.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Knowledge of geriatric oral hygiene scale
Tidsramme: through study completion, an average of 4 weeks
|
There were 10 items to evaluate the participants' knowledge of the geriatric oral hygiene scale Each item had three response options: true, false, and unknown.
The total score ranged from 0 to 10 and a higher score indicated a higher level of knowledge of geriatric oral hygiene.
|
through study completion, an average of 4 weeks
|
Attitudes of geriatric oral hygiene scale
Tidsramme: through study completion, an average of 4 weeks
|
The attitudes of geriatric oral hygiene scale included seven items.
Each item was scored on a five-point Likert-type scale ranging from 1 (strongly disagree) to 5 (strongly agree).
The total score ranged from 5 to 35 and a higher score indicated a positive attitude toward geriatric oral hygiene.
|
through study completion, an average of 4 weeks
|
Self-efficacy of geriatric oral hygiene scale
Tidsramme: through study completion, an average of 4 weeks
|
The self-efficacy of geriatric oral hygiene scale included ten items.
Each item was scored on a five-point Likert-type scale ranging from 1 (strongly disagree) to 5 (strongly agree) and the higher score was for a higher level of self-efficacy of geriatric oral hygiene, vise versa.
The total score ranged from 5 to 50.
|
through study completion, an average of 4 weeks
|
Behavioral intention of geriatric oral hygiene scale
Tidsramme: through study completion, an average of 4 weeks
|
The behavioral intention scale of the geriatric oral hygiene included ten items.
Each item was scored on a five-point Likert-type scale ranging from 1 (strongly disagree) to 5 (strongly agree), with a higher score indicated a higher level of the behavioral intention of geriatric oral hygiene.
The total score ranged from 5 to 50.
|
through study completion, an average of 4 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Pei-Chao Lin, Kaohsiung Medical University
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
23. marts 2021
Primær færdiggørelse (Faktiske)
19. april 2021
Studieafslutning (Faktiske)
12. november 2021
Datoer for studieregistrering
Først indsendt
30. december 2021
Først indsendt, der opfyldte QC-kriterier
9. februar 2022
Først opslået (Faktiske)
21. februar 2022
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
21. februar 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
9. februar 2022
Sidst verificeret
1. december 2021
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- KMUHIRB-SV(II)-20200062
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Virtual reality
-
Palo Alto UniversityAfsluttet
-
The Opole University of TechnologyAfsluttet
-
Shenandoah UniversityAfsluttetVirtual realityForenede Stater
-
The Opole University of TechnologyIRCCS San Camillo, Venezia, ItalyAfsluttet
-
The Methodist Hospital Research InstituteNational Institute on Aging (NIA)AfsluttetVirtual realityForenede Stater
-
Seoul National University Bundang HospitalAfsluttet
-
Hacettepe UniversityAfsluttet
-
Sunnybrook Health Sciences CentreIkke rekrutterer endnu
-
Medical University of LodzNational Center for Research and Development, Poland; Senopi AGRekruttering
Kliniske forsøg med Virtual Reality Usage on Oral Care Knowledge
-
University of TorontoIkke rekrutterer endnuVirtual reality | Kirurgisk Uddannelse | Ortopædisk træning
-
National Taiwan Normal UniversityAfsluttet
-
Marta Peciña, MD PhDRekrutteringDepression | Større depressiv lidelseForenede Stater