Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
ID06638515

Effects of Walking Apnea At Low Lung Volume on Hypoalgesia

Led by Universidad Rey Juan Carlos · Updated on 2024-10-15

60

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how a 6-minute session of intermittent walking apneas at low lung volume affects pain sensitivity in healthy adults aged 18 to 64 years. The study also looks at how this type of breathing impacts cardiovascular and respiratory functions during the exercise. This randomized controlled trial aims to better understand the body's response to this specific walking and breathing pattern. Participants are divided into two groups: one group walks on a treadmill at 6 km/h with a 10% slope while performing intermittent apneas (holding their breath) for 5 seconds followed by normal breathing for 5 seconds during 6 minutes. The other group walks under the same conditions but breathes normally throughout. This intervention is designed to compare the effects of breathing patterns on pain response and physiological measures. During the study, researchers will measure pain pressure threshold on various body areas before and up to 30 minutes after the intervention. Other assessments include stress levels, sleep quality, physical activity questionnaires before the session, and monitoring oxygen saturation, blood pressure, heart rate, and perceived exertion during and after walking. The study runs from November 2024 to May 2025 and involves healthy volunteers between 18 and 65 years old.

CONDITIONS

Brief Title

Effects of Walking Apnea At Low Lung Volume on Hypoalgesia

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Asymptomatic subjects aged between 18 and 64 years.
Not Eligible

You will not qualify if you...

  • 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.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Single session

Participants either walk on a treadmill at 6 km/h with intermittent apneas at low lung volume or walk normally with regular breathing for 6 minutes.

1 in-person visit

Trial Site Locations

Total: 1 location

1

CSEU LaSalle

Madrid, Spain

Actively Recruiting

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Research Team

F

Francisco de Asís Fernandez

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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