Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
NCT07498816

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

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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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