Clinical Trials Logo

Clinical Trial Summary

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.


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03833674
Study type Interventional
Source University of Florida
Contact
Status Completed
Phase N/A
Start date August 15, 2020
Completion date February 20, 2024

See also
  Status Clinical Trial Phase
Recruiting NCT04295538 - Safety And Efficacy Study Of Intravenous (IV) Administration Of Elezanumab To Assess Change In Upper Extremity Motor Score (UEMS) In Adult Participants With Acute Traumatic Cervical Spinal Cord Injury (SCI) Phase 2
Completed NCT01232907 - The Effects of L-carnitine on Fatigue in Spinal Cord Injury Phase 2
Not yet recruiting NCT01771159 - Tissue Bonding Cystostomy(TBC) Phase 1
Completed NCT02052024 - Myobloc Atrophy Study Phase 4
Completed NCT02469675 - Brain and Nerve Stimulation for Hand Muscles in Spinal Cord Injury and ALS N/A
Completed NCT00488280 - Restoring Walking in Non-ambulatory Children With Severe Chronic Spinal Cord Injury (SCI) (Kids STEP Study) Phase 1
Recruiting NCT01772810 - Safety Study of Human Spinal Cord-derived Neural Stem Cell Transplantation for the Treatment of Chronic SCI Phase 1