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BreathinG-induced Myocardial and Cerebral Perfusion in Anxiety Disorders (B-GLAD)

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McGill University

Status

Enrolling

Conditions

Generalized Anxiety Disorder
Oxygenation Sensitive CMR

Treatments

Diagnostic Test: Cardiac MRI

Study type

Observational

Funder types

Other

Identifiers

NCT05574140
2020-6298

Details and patient eligibility

About

This study aims to view variations in MRI measurements of the heart and the brain in people with anxiety versus healthy volunteers. The MRI measurements used will be Oxygenation-Sensitive Cardiac MRI (OS-CMR), a recent type of MRI which is safe, fast, and non-invasive.

Full description

The investigators will prospectively analyze OS-CMR data from patients with a generalized anxiety disorder from one site. The investigators will observe how an anxiety disorder affects the OS-CMR data. In a follow-up MRI scan, the investigators will look at the OS-CMR of a subgroup who have anxiety disorder and are also undertaking cognitive behavioural therapy to asses how and if this therapy affects the OS-CMR data.

Enrollment

84 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Patient population:

Age 18-55,

  • Confirmation of an anxiety disorder as identified by the PSWQ,
  • No known, current or history, of significant medical conditions that may affect or directly involve the neurological, cardiovascular or respiratory system (except anxiety and depression)
  • Non-smoker

Healthy Volunteers:

  • Age 18-55
  • No known, current or history, of significant medical conditions that may affect or directly involve the neurological, cardiovascular or respiratory system
  • Non-smoker

Exclusion criteria

  • General MRI contraindications: pacemakers, defibrillating wires, implanted defibrillators, intracranial aneurysm clips, metallic foreign bodies in the eyes, pregnancy
  • History of significant neurological disease or illness that is not anxiety (e.g. Dementia, stroke)
  • Hemodynamically unstable conditions
  • Significant or uncontrolled arrhythmias
  • Severe pulmonary disease
  • Recent (<90 days) myocardial infarction
  • Recent (<90 days) surgery or coronary intervention
  • Consumption of caffeine (caffeinated beverages, coffee, tea, cocoa, chocolate) within 12h of the exam
  • Use of benzodiazepines or other short-acting anxiety medications (<1 day)

Trial design

84 participants in 2 patient groups

Patient Population
Description:
Participants diagnosed with Generalized Anxiety Disorder
Treatment:
Diagnostic Test: Cardiac MRI
Healthy Volunteers
Description:
Participants with no pre-existing conditions and who are on no medications.
Treatment:
Diagnostic Test: Cardiac MRI

Trial contacts and locations

1

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Central trial contact

Elizabeth Konidis, Master; Mayssa Moukarzel

Data sourced from clinicaltrials.gov

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