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Effect of Non-invasive Magnetic Stimulation of the Brain on Breathlessness in Healthy Individuals.

Not Applicable
Recruiting
Conditions
Dyspnea
Interventions
Device: Sham or actual non-invasive (Magnetic) brain stimulation
Registration Number
NCT05623696
Lead Sponsor
Oxford Brookes University
Brief Summary

The purpose of this study is to see if the front part of the brain called the "Dorsolateral Prefrontal Cortex" (DLPFC) has a role in our ability to feel breathlessness. The experiment will use a device that sits on the top of the head which produces a magnetic field that penetrates the scalp and excites the brain tissue directly under it. This procedure is called repetitive transcranial magnetic stimulation (rTMS), it is a painless procedure and known to be safe in healthy individuals. Previous research has shown that the pain felt when capsaicin, the active ingredient in 'chilli' powder, is applied to the hand is reduced by applying the rTMS on the scalp directly above the DLPFC part of the brain. In this experiment we want to see if breathlessness is also reduced. We will use a breathing task that will generate a moderate amount of breathlessness by adding a small amount of carbon dioxide to the inhaled air, while preventing the increase in the amount of breathing we would normally see in response to this. If we find that breathlessness produced by this breathing task is reduced after rTMS over the DLPFC, this may lead to new drugs that target this part of the brain in patients suffering from breathlessness due to heart or lung disease. The study will also improve our knowledge of how the brain enables us to feel breathlessness

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
16
Inclusion Criteria

healthy individuals, over 18 years old, with no history of heart, lung or neurological conditions

Exclusion Criteria
  • Any history of respiratory problems (including Asthma that involves regular use of inhalers)
  • Any history of heart or circulatory problems (e.g. palpitations, arrhythmias, angina, BP)
  • Any history of epilepsy, convulsions or seizures, migraines, or fainting
  • Any history of anxiety disorders (e.g. panic attacks)
  • Any history of serious head injury or brain surgery
  • Any metal parts in the head (except dental wire)
  • Any implants (e.g. pacemaker, insulin pump, neurostimulator)
  • Pregnancy or problems with alcohol or drug abuse.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Stimulation of Left DLPFCSham or actual non-invasive (Magnetic) brain stimulationIntervention applied to Left DLPFC located by the BeamF3 technique
Stimulation of Right DLPFCSham or actual non-invasive (Magnetic) brain stimulationIntervention applied to Right DLPFC located by the BeamF3 technique
Sham StimulationSham or actual non-invasive (Magnetic) brain stimulationSham intervention applied to either the left or right DLPFC
Primary Outcome Measures
NameTimeMethod
Air hungerAverage of 4 steady state ratings in the last minute of air hunger tests

Visual analog scale ratings of air hunger

Secondary Outcome Measures
NameTimeMethod
Dyspnoea-12 total, physical and emotion scoresAdministered immediately following pre and post intervention air hunger tests in relation to the "test just completed"

Multidimensional D12-Questionnaire

Mood assessmentimmediately following pre and post intervention air hunger tests

Bond Lader Mood questionnaire

Trait and state anxiety scoresimmediately following pre and post intervention air hunger tests

Spielberger's State-Trait anxiety inventory

Trial Locations

Locations (1)

Oxford Brookes University

🇬🇧

Oxford, Oxfordshire, United Kingdom

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