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Study Effects of Intermittent Hypoxia on Restoring Hand Function Following SCI

Primary Purpose

Spinal Cord Injury

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Acute Intermittent Hypoxia (AIH)
SHAM-Intermittent Room Air
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinal Cord Injury focused on measuring spinal cord injury, low oxygen, strength, motor control

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • age 18 and 65 years
  • medical clearance to participate
  • lesion below the 5th cervical spinous process (C5) and above the first thoracic spinous process (T1) with non-progressive etiology
  • classified as motor-incomplete injury greater than 12 months
  • independent breathing

Exclusion Criteria:

  • Concurrent severe medical illness (i.e., infection, cardiovascular disease, ossification, recurrent autonomic dysreflexia, unhealed decubiti, and history of cardiac or pulmonary complications)
  • Pregnant women because of the unknown affects of acute intermittent hypoxia on pregnant women and fetus
  • Concomitant acquired brain injury
  • History of seizures, brain injury, and/or epilepsy
  • Diagnosed with obstructive sleep apnea
  • Undergoing concurrent physical therapy
  • Any contraindications to EMG testing procedures (skin sensitivity)
  • Any contraindications to passive movement of the limbs
  • Score of < 24 on Mini-Mental Exam

Sites / Locations

  • Emory Center for Rehabilitation Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

AIH/Sham

Sham/AIH

Arm Description

Subjects with chronic, motor-incomplete SCI receive AIH and then SHAM

Subjects with chronic, motor-incomplete SCI receive SHAM and then AIH

Outcomes

Primary Outcome Measures

Hand grasp

Secondary Outcome Measures

Grip strength

Full Information

First Posted
January 4, 2011
Last Updated
January 23, 2016
Sponsor
Emory University
Collaborators
University of Saskatchewan, University of Wisconsin, Madison
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1. Study Identification

Unique Protocol Identification Number
NCT01272336
Brief Title
Study Effects of Intermittent Hypoxia on Restoring Hand Function Following SCI
Official Title
Intermittent Hypoxia Promotes Restoration of Hand Function Following SCI
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
December 2010 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
October 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University
Collaborators
University of Saskatchewan, University of Wisconsin, Madison

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of the study is to examine the effects of repeated breathing episodes of mild intermittent hypoxia (reduced oxygen) training on hand strength and grasping ability following cervical spinal injury, and to determine whether these changes result in improved hand function. If so, such changes may indicate hypoxia-induced spinal plasticity (ability of the nervous system to strengthen neural pathways based on new experiences), which could result in improvements in hand use for persons with spinal cord injury (SCI).
Detailed Description
The goal of the study is to examine the effects of repeated breathing episodes of mild intermittent hypoxia (reduced oxygen) training on hand strength and grasping ability following cervical spinal injury, and to determine whether these changes result in improved hand function. If so, such changes may indicate hypoxia-induced spinal plasticity (ability of the nervous system to strengthen neural pathways based on new experiences), which could result in improvements in hand use for persons with spinal cord injury (SCI). This idea stems from animal studies on respiration, in which investigators have shown that intermittent hypoxia induces spinal plasticity, strengthening neural connections within the spinal cord by a mechanism known as respiratory long-term facilitation. Exposure to mild hypoxia triggers oxygen sensors in the nervous system resulting in a cascade of events, including increased production of key proteins and, increased sensitivity of spinal cord circuitry necessary for improved respiration. Because previous work using animal models has shown that similar events occur along non-respiratory pathways, the investigators propose to investigate whether a comparable dosing scheme of daily, mild intermittent hypoxia can positively affect upper limb function in persons with cervical SCI. First, the investigators hypothesize that daily exposure of intermittent hypoxia training (7 consecutive days) will result in a sustained improvement in rat forelimb function that is dose-dependent. To test this hypothesis, the investigators will quantify the effects of variations in the number of intermittent hypoxia episodes on forelimb function in cervical spinal injured rats. Second, the investigators hypothesize that daily exposure of intermittent hypoxia training will improve hand function in persons with cervical spinal injury. To test this hypothesis, the investigators will quantify the effect of mild intermittent hypoxia exposure, using a protocol derived from the animal model, on volitional grip strength and grasp function in persons with cervical SCI. The effects of mild intermittent hypoxia, known to increase spinal motor activity, will be assessed as a possible therapeutic intervention to promote functionally useful hand recovery. Results from this study will be valuable for identifying novel strategies to control spinal neuron excitability and for improving motor function in persons with spinal cord injury.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injury
Keywords
spinal cord injury, low oxygen, strength, motor control

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
AIH/Sham
Arm Type
Active Comparator
Arm Description
Subjects with chronic, motor-incomplete SCI receive AIH and then SHAM
Arm Title
Sham/AIH
Arm Type
Active Comparator
Arm Description
Subjects with chronic, motor-incomplete SCI receive SHAM and then AIH
Intervention Type
Drug
Intervention Name(s)
Acute Intermittent Hypoxia (AIH)
Other Intervention Name(s)
Hypoxia air mixture
Intervention Description
Participants will breath 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 FIO2=0.09±0.02 (hypoxia) air for 15 minutes.Participants will receive treatment for up to seven visits.
Intervention Type
Other
Intervention Name(s)
SHAM-Intermittent Room Air
Other Intervention Name(s)
Room air mixture
Intervention Description
This is a sham intervention to the AIH intervention. Participants will breath 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 FIO2=0.21±0.02 (normoxia). Participants will receive treatment for up to seven visits.
Primary Outcome Measure Information:
Title
Hand grasp
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Grip strength
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: age 18 and 65 years medical clearance to participate lesion below the 5th cervical spinous process (C5) and above the first thoracic spinous process (T1) with non-progressive etiology classified as motor-incomplete injury greater than 12 months independent breathing Exclusion Criteria: Concurrent severe medical illness (i.e., infection, cardiovascular disease, ossification, recurrent autonomic dysreflexia, unhealed decubiti, and history of cardiac or pulmonary complications) Pregnant women because of the unknown affects of acute intermittent hypoxia on pregnant women and fetus Concomitant acquired brain injury History of seizures, brain injury, and/or epilepsy Diagnosed with obstructive sleep apnea Undergoing concurrent physical therapy Any contraindications to EMG testing procedures (skin sensitivity) Any contraindications to passive movement of the limbs Score of < 24 on Mini-Mental Exam
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Randy D Trumbower, PT, PhD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emory Center for Rehabilitation Medicine
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
28972191
Citation
Trumbower RD, Hayes HB, Mitchell GS, Wolf SL, Stahl VA. Effects of acute intermittent hypoxia on hand use after spinal cord trauma: A preliminary study. Neurology. 2017 Oct 31;89(18):1904-1907. doi: 10.1212/WNL.0000000000004596. Epub 2017 Sep 29.
Results Reference
derived

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Study Effects of Intermittent Hypoxia on Restoring Hand Function Following SCI

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