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Effects of Static Apnea at High Lung Volume on Hypoalgesia, Cardiovascular Function and Respiratory Function

C

Centro Universitario La Salle

Status and phase

Enrolling
Phase 3

Conditions

Hypercapnia
Apnea
Hypoxia
Pain

Treatments

Other: Voluntary apnoea

Study type

Interventional

Funder types

Other

Identifiers

NCT06150677
CSEULS-PI-015/2023

Details and patient eligibility

About

The aim of this randomized controlled study is to explore the hypoalgesic response of a 6 minutes of intermittent static apneas training session at high lung volume in healthy subjects; also, as secondary objectives, to analyze the cardiovascular and respiratory response produced during the intervention.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Asymptomatic subjects aged between 18 and 64 years.

Exclusion criteria

  • Cardiovascular, respiratory, metabolic, neurological or osteomuscular signs or pathologies.
  • History of epilepsy.
  • Pregnant.
  • Pharmacological treatment.
  • Participants who present any type of pain on the day of the measurements or who have frequently suffered pain during the previous 4 weeks.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Static apnea at High Lung Volume
Experimental group
Description:
Participants will remain at rest in the supine position for 6 minutes. Participants in the experimental group will perform intermittent apneas at high lung volume with a density of 30 seconds, followed by a normal breath of 10 seconds (9 cycles of 30s apnea - 10s normal breathing, until completing the 6 minutes).
Treatment:
Other: Voluntary apnoea
Static at normal breathing
No Intervention group
Description:
Participants will remain at rest in the supine position for 6 minutes. Participants in the control group will remain breathing normally for these 6 minutes

Trial contacts and locations

1

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Central trial contact

Fran DeAsís-Fernández

Data sourced from clinicaltrials.gov

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