Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04007380

Psychosocial, Cognitive, and Behavioral Consequences of Sleep-disordered Breathing After SCI

Led by University Health Network, Toronto · Updated on 2024-12-11

24

Participants Needed

1

Research Sites

309 weeks

Total Duration

On this page

Sponsors

U

University Health Network, Toronto

Lead Sponsor

T

The Craig H. Neilsen Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

This clinical trial will examine the efficacy of continuous positive airway pressure (CPAP) therapy in improving psychosocial, neurocognitive and behavioral consequences of moderate-to-severe sleep-related breathing disorders (SRBDs) in people living with spinal cord injury (SCI).

CONDITIONS

Official Title

Psychosocial, Cognitive, and Behavioral Consequences of Sleep-disordered Breathing After SCI

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • English-speaking adults 18 years of age or older
  • Traumatic cervical or thoracic spinal cord injury between levels C5 and T10
  • Moderate or severe spinal cord injury classified as AIS A, B, or C
  • Injury occurred at least 2 months prior to enrollment
  • Presence of clinical warning symptoms or signs for sleep-related breathing disorders
Not Eligible

You will not qualify if you...

  • Non-traumatic spinal cord disease with risk for neurologic progression
  • Diseases affecting the central nervous system
  • Preexisting chronic pain before injury
  • Psychiatric disorders interfering with study compliance
  • Neuromuscular diseases
  • Current substance misuse
  • History of primary hypersomnia
  • Hypothyroidism
  • Moderate or severe iron deficiency anemia
  • Active infections
  • Kidney failure
  • Epilepsy
  • Chronic fatigue syndrome
  • Vitamin B12 deficiency

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Lyndhurst Centre, KITE - TRI UHN

Toronto, Ontario, Canada

Actively Recruiting

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Research Team

M

Mitsue Aibe, MD

CONTACT

J

Julio Furlan, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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