Actively Recruiting
Impact of Immersive Virtual Reality (IVR) on Respiratory Effort: A Pilot Study in Healthy Adults
Led by Pontificia Universidad Catolica de Chile · Updated on 2026-03-27
10
Participants Needed
1
Research Sites
62 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This pilot randomized crossover study will evaluate the acute effects of immersive virtual reality (IVR) on respiratory effort during submaximal exercise in healthy adults. Dyspnea and increased respiratory effort are influenced not only by mechanical and metabolic factors, but also by emotional and central neural inputs. IVR has shown potential to reduce anxiety, promote relaxation, and modulate physiological responses, but its direct effect on respiratory effort has not been adequately studied. Healthy adults will complete two experimental exercise sessions: one session with IVR and one session without IVR, in randomized order. In both conditions, participants will perform a 6-minute constant-load cycling test at a submaximal workload individualized from a prior incremental exercise test. Respiratory effort will be assessed continuously using esophageal pressure monitoring. Additional measurements will include ventilatory variables, perceived dyspnea, acute state anxiety, heart rate, oxygen saturation, and heart rate variability. The primary aim is to determine whether IVR reduces respiratory effort compared with the control condition. This pilot study is intended to provide physiological evidence on the potential role of IVR as a non-pharmacological strategy to modulate respiratory effort and dyspnea, and to inform future research in clinical populations.
CONDITIONS
Official Title
Impact of Immersive Virtual Reality (IVR) on Respiratory Effort: A Pilot Study in Healthy Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy adults aged 18-40 years
- Ability to perform cycle ergometer exercise testing
- No known history of cardiovascular, pulmonary, neurological, or metabolic disease
You will not qualify if you...
- Current respiratory symptoms or acute illness
- Known cardiovascular, pulmonary, neurological, or metabolic disease
- Use of medications that may affect respiratory or cardiovascular responses to exercise
- Contraindications to exercise testing according to standard clinical guidelines
- Pregnancy
- Inability to tolerate placement of an esophageal balloon catheter
- Susceptibility to motion sickness or discomfort with immersive virtual reality devices
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Escuela de Ciencias de la Salud UC. Departamento de Kinesiología.
Santiago, Santiago Metropolitan, Chile, 6904411
Actively Recruiting
Research Team
G
Gonzalo A Valdivia Lobos, Physiotherapy
CONTACT
F
Felipe Damiani R., PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
OTHER
Number of Arms
2
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