Assessment of Exercise Capacity in Virtual Reality
2 november 2020 bijgewerkt door: Sebastian Rutkowski, The Opole University of Technology
Evaluation of the Impact of Immersive Virtual Reality During the Submaximal Cardiorespiratory Fitness
The 20th century brought a dynamic development of new technologies, including virtual reality (VR).
VR is an artificial image generated by IT technologies.
It is most often associated with entertainment, but has a much wider application in other fields.
The aim of the study is to assess the influence of the application of immersive virtual reality during an exercise capacity test on a bicycle ergometer.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Scientists suggests that there are four types of virtual reality: immersive virtual reality, desktop virtual reality (i.e., low-cost homebrew virtual reality), projection virtual reality, and simulation virtual reality.
The sense of presence or immersion is a critical feature distinguishing virtual reality from other types of computer applications.
It seems interesting whether immersion in virtual reality can influence the assessment of exercise capacity.
The aim of the study is to assess the influence of the application of immersive virtual reality during an exercise capacity test on a bicycle ergometer.
It is assumed that an exercise capacity test on a cycloergometer will be performed in a traditional form and in a virtual reality.
Studietype
Ingrijpend
Inschrijving (Werkelijk)
70
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Opole, Polen, 45-758
- Institute of Physiotherapy, Department of Physical Education and Physiotherapy, Opole University of Technology
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
20 jaar tot 25 jaar (Volwassen)
Accepteert gezonde vrijwilligers
Ja
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
1. Female and male, age: 20-25 years
Exclusion Criteria:
- diagnosed internal diseases
- diseases and injuries of the locomotors system impairing the function of transport 3 Cognitive disorders preventing contact with the patient, Mini-Mental State Examination < 24 points.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Diagnostisch
- Toewijzing: Gerandomiseerd
- Interventioneel model: Crossover-opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Traditional exercise capacity test
Patients of the Ministry of the Interior and Administration hospital in Głuchołazy with a diagnosed disease unit of Chronic Obstructive Pulmonary Disease (COPD).
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Patients will be assessed by symptom-limited maximal cardiopulmonary exercise testing (CPET) following a 25W, tree-minute stage, beginning at 25W (healthy volunteers will start the test with a load of 50W).
For both sexes and arms, participants will be instructed during the test to remain at the frequency between 60 to 80 rotations per minute (rpm).
Heart rate (HR) will be continuously recorded using a monitor Polar H10.
Andere namen:
Patients will be assessed by symptom-limited maximal cardiopulmonary exercise testing (CPET) following a 25W, tree-minute stage, beginning at 25W (healthy volunteers will start the test with a load of 50W).
For both sexes and arms, participants will be instructed during the test to remain at the frequency between 60 to 80 rotations per minute (rpm).Heart rate (HR) will be continuously recorded using a monitor Polar H10.
VR HTC Vive Pro goggles along with VR health care (aerobic exercise) VR Cycling software will be used for stimulation throughout the duration of the test.
The HTC Vive Tracker device will be also use to link images in virtual reality with the pedal speed.
Andere namen:
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Experimenteel: Immersive virtual reality exercise capacity test
Healthy volunteers, Students of Department of Physical Education and Physiotherapy, Opole University of Technology, Opole, Poland
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Patients will be assessed by symptom-limited maximal cardiopulmonary exercise testing (CPET) following a 25W, tree-minute stage, beginning at 25W (healthy volunteers will start the test with a load of 50W).
For both sexes and arms, participants will be instructed during the test to remain at the frequency between 60 to 80 rotations per minute (rpm).
Heart rate (HR) will be continuously recorded using a monitor Polar H10.
Andere namen:
Patients will be assessed by symptom-limited maximal cardiopulmonary exercise testing (CPET) following a 25W, tree-minute stage, beginning at 25W (healthy volunteers will start the test with a load of 50W).
For both sexes and arms, participants will be instructed during the test to remain at the frequency between 60 to 80 rotations per minute (rpm).Heart rate (HR) will be continuously recorded using a monitor Polar H10.
VR HTC Vive Pro goggles along with VR health care (aerobic exercise) VR Cycling software will be used for stimulation throughout the duration of the test.
The HTC Vive Tracker device will be also use to link images in virtual reality with the pedal speed.
Andere namen:
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Exercise Testing- cycle ergometer
Tijdsspanne: First or second day of the assessment - the traditional exercise test
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The exercise test on an electronically-braked cycle ergometer (Lode Excalibur Sport PFM) was used for evaluation.
Test began with a unloaded cycling for 3 minutes, then 50W for 3 minutes followed by an incremental phase in which work rate increased by 25 watts every 3 minutes.
Heart rate (HR) was continuously recorded.
These submaximal tests were terminated when the subjects reached 85% of the age-predicted maximal HR (calculated as 220 - age)
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First or second day of the assessment - the traditional exercise test
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HRV
Tijdsspanne: First or second day of the assessment - the exercise test in VR
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The Polar H10 monitor (Polar Electro Oy Inc., Kempele, Finland) was employed to record heart rate series at a sampling frequency of 1000 Hz.
All HRV analyses were carried out with the Kubios HRV Premium version 3.3.1 (HRV analysis, University of Eastern Finland).
The R-R interval series were filtered with the artifact correction algorithm which was set at the automatic mode.
Time- and frequency-domain HRV parameters were analyzed.
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First or second day of the assessment - the exercise test in VR
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Onderzoekers
- Hoofdonderzoeker: Sebastian Rutkowski, PhD, The Opole University of Technology
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
17 december 2019
Primaire voltooiing (Werkelijk)
27 juni 2020
Studie voltooiing (Werkelijk)
27 september 2020
Studieregistratiedata
Eerst ingediend
5 december 2019
Eerst ingediend dat voldeed aan de QC-criteria
10 december 2019
Eerst geplaatst (Werkelijk)
12 december 2019
Updates van studierecords
Laatste update geplaatst (Werkelijk)
4 november 2020
Laatste update ingediend die voldeed aan QC-criteria
2 november 2020
Laatst geverifieerd
1 november 2020
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Andere studie-ID-nummers
- OpoleUofTech1
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .