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Completed

NCT Number: NCT03833674

FLO2 for Recovery After SCI

Acute intermittent hypoxia (AIH) involves short (~1-2min) bouts of breathing low oxygen air to stimulate spinal neuroplasticity. Studies in rodents and humans indicate that AIH improves motor function after spinal cord injury (SCI). This study will use a double blind, cross-over design to test if the combination of AIH and respiratory strength training improves breathing function more than either approach alone in adults with chronic SCI.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Brooks Rehabilitation Hospital

Jacksonville, Florida, 32216, United States

About this study

Spinal cord injury (SCI) disrupts neural pathways to respiratory motor neurons, causing muscle paralysis and decreased breathing capacity. Since respiratory impairment is the major cause of illness and death with SCI, it is critical to devise new strategies to restore breathing function.

Repetitive exposure to brief episodes of low oxygen (acute intermittent hypoxia or AIH) has demonstrated to increase respiratory function in humans with chronic SCI. Additionally pre-clinical studies demonstrate that AIH-induced functional benefits are enhanced by combining AIH with task-specific training. The investigator's central hypothesis is that combined daily AIH (dAIH) and respiratory strength training will elicit greater and more sustained gains in respiratory function than either treatment alone in people with chronic SCI.

This study is a double-blind, randomized, cross-over design where participants will complete 4 random-ordered blocks, consisting of a 5-day intervention followed by a 3-week washout period, during which 1-day, 3-day, and 1-week post-tests will be conducted. Participants will include 53 adults with chronic, incomplete SCI with >20% respiratory impairment based on maximal inspiratory or expiratory pressure generation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Chronic incomplete SCI for ≥ 1 year at or below C-1 to T-12
  • Incomplete SCI based on residual sensory and motor function below the level of the injury or injury classification of B, C, D at initial screening according to the American Spinal Injury Association Impairment Classification and the International Standards for the Neurological Classification of SCI

-OR-

Chronic complete SCI for ≥ 1 year at or below C-4 to T-12

  • Complete SCI based on the absence of residual sensory or motor function below the level of injury or injury classification of A at initial screening according to the American Spinal Injury Association Impairment Classification and the International Standards for the Neurological Classification of SCI.
  • Medically stable with clearance from physician
  • SCI due to non-progressive etiology
  • >20% impairment in maximal inspiratory or expiratory pressure generation, relative to established normative values.

Exclusion criteria

  • Current diagnosis of an additional neurologic condition such as multiple sclerosis, Parkinson's disease, stroke, or brain injury
  • Presence of unstable or uncontrolled medical conditions such as cardiovascular disease, myocardial infarction, <1 year lung disease, infections, hypertension, heterotopic ossification.
  • Severe neuropathic pain
  • Known pregnancy
  • Severe recurrent autonomic dysreflexia
  • History of seizure disorder < 1 year

Treatment and study plan

Daily AIH Block

Other

Daily sessions of AIH (dAIH) with use of short episodes of low oxygen (9% O2)

Other names: dAIH Block

Sham dAIH Block

Other

Daily sessions of sham dAIH which includes breathing room air (21% O2)

Respiratory Strength Training Block

Other

Respiratory strength training using a hand-held device that resists inspiration or expiration.

AIH + Strength Training Block

Other

AIH followed by respiratory strength training.

Primary outcomes

  1. Change in maximal inspiratory pressure

    Time frame: Baseline, Day 1, Day 6, Day 8, Day 15

    Maximal inspiratory pressure is a non-invasive measure of the maximal force achieved when breathing in against an occluded airway.

  2. Change in maximal expiratory pressure

    Time frame: Baseline, Day 1, Day 6, Day 8, Day 15

    Maximal expiratory pressure is a non-invasive measure of the maximal force generated when breathing out against an occluded airway.

Sponsors and collaborators

Lead sponsor

University of Florida

Other

Collaborators

  • Brooks Rehabilitation
  • United States Department of Defense

Registry information

Official study title

Acute Intermittent Hypoxia and Respiratory Strength Training to Improve Breathing Function After Spinal Cord Injury

Important dates

Study start
2020
Primary completion
2024
Study completion
2024
First posted
Feb 7, 2019
Registry last updated
May 29, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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