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Acute Intermittent Hypoxia on Leg Function Following Spinal Cord Injury

Repetitive Exposure of Intermittent Hypoxia to Enhance Walking Recovery in Persons With Chronic Spinal Cord Injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02274116
Enrollment
30
Registered
2014-10-24
Start date
2014-10-01
Completion date
2027-11-01
Last updated
2026-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Injuries

Keywords

acute intermittent hypoxia, walking, spasticity, incomplete spinal cord injury, breathing, strength

Brief summary

The purpose of this study is to determine how the nervous system controlling leg muscles is altered following spinal cord injury and how they may be affected by brief periods of low oxygen inhalation over time. The investigators hypothesize: * Acute intermittent hypoxia (AIH) exposure will increase maximum voluntary leg strength in persons with incomplete cervical spinal cord injury (SCI) * AIH exposure will increase multijoint reflex excitability of leg muscles in persons with incomplete cervical SCI * AIH exposure will increase walking performance in persons with incomplete cervical SCI

Detailed description

Accumulating evidence suggests that repeatedly breathing low oxygen levels for brief periods (termed intermittent hypoxia) is a safe and effective treatment strategy to promote meaningful functional recovery in persons with chronic spinal cord injury. Repetitive exposure to mild hypoxia triggers a cascade of events in the spinal cord, including new protein synthesis and increased sensitivity in the circuitry necessary for breathing and walking. Recently, the investigators demonstrated that daily (5 consecutive days) of intermittent hypoxia stimulated walking enhancement in persons with chronic spinal cord injury. Despite these exciting findings, important clinical questions remain. For example, the investigators do not know if prolonged, but less intense intermittent hypoxia induces longer-lasting motor recovery as has been shown in rat models. The investigators hypothesize that repetitive exposures to modest bouts of low oxygen will enhance and prolong walking recovery in persons with chronic spinal cord injury. The investigators anticipate intermittent hypoxia-induced improvements in overground walking ability, likely due to greater balance in excitatory and inhibitory neural transmission. Whereas excitatory inputs drive walking, inhibitory inputs sculpt and coordinate muscle activity; yet so often remain compromised after chronic injury. Thus, the investigators also predict that repetitive exposures to intermittent hypoxia will result in improved inhibition and subsequently enhance muscle coordination during walking. The investigators will use multiple experimental approaches, including muscle electromyography, measurements of walking dynamics and stretch reflexes. Finally, it is critical to assure that repetitive exposures to intermittent hypoxia do not elicit pathologies characteristic of more severe, chronic hypoxia experienced by individuals with obstructive sleep apnea. The investigators will confirm that repetitive exposure to mild bouts of intermittent hypoxia is safe.

Interventions

Participants will breathe intermittent room air via air generators. The generators will fill reservoir bags attached to a non-rebreathing face mask. Oxygen concentration will be continuously monitored to ensure delivery of fraction of inspired oxygen (FIO2)=0.21±0.02 (normoxia). Participants will receive treatment 5 times per week for 2 weeks.

Participants will breathe intermittent low oxygen via air generators. The generators will fill reservoir bags attached to a non-rebreathing face mask. Oxygen concentration will be continuously monitored to ensure delivery of fraction of inspired oxygen (FIO2)=0.10±0.02 (hypoxia). Participants will receive treatment 5 times per week for 2 weeks.

Sponsors

Spaulding Rehabilitation Hospital
Lead SponsorOTHER
Foundation Wings For Life
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* 18 to 75 years old (the latter to reduce likelihood of heart disease); * medically stable with clearance from physician to participate; * motor---incomplete SCI at C2---L5 with non---progressive etiology; * \>6 months since SCI to ensure minimal confounds of spontaneous neurological recovery; * those classified as ambulatory must have the ability to advance one step overground without human assistance.

Exclusion criteria

* concurrent illness, including unhealed decubiti, severe neuropathic or chronic pain syndrome, infection, cardiovascular disease, osteoporosis (history of fractures), active heterotopic ossification, or known history of peripheral nerve injury to legs; * less than 24 on the Mini-mental Exam; * recurrent autonomic dysreflexia * cardiopulmonary complications * concurrent physical therapy * pregnancy because of unknown effects of AIH on a fetus, although women will not otherwise be excluded

Design outcomes

Primary

MeasureTime frameDescription
Change in overground walking enduranceBaseline, immediately following intervention (day 5), and at 1, 2, and 4 weekswalking endurance (6 minute walk test - how far one can walk in 6 minutes)

Secondary

MeasureTime frameDescription
Change in overground walking speedBaseline, immediately following intervention (day 5), and at 1, 2, and 4 weekswalking speed (10 meter walk test - how fast one can walk in 10 meters)

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORRandy D Trumbower, PT, PhD

Spaulding Rehabilitation Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 21, 2026