Established Stroke, Ischemic Stroke, Stroke
Conditions
Keywords
Hyperbaric Oxygen, HBOT, Hyperbaric Chamber, Pressurized Oxygen
Brief summary
The purpose of this study is to examine the role of Hyperbaric Oxygen Therapy (HBOT) in improving neurological function in patients who are 6 to 36 months post ischemic stroke.
Detailed description
The purpose of this study is to examine the role of Hyperbaric Oxygen Therapy (HBOT) in improving neurological function in patients who are 6 to 36 months post ischemic stroke. Hyperbaric oxygen therapy (HBOT) involves the administration of inhaled 100% oxygen at increased ambient pressure inside a closed vessel. HBOT produces greatly elevated arterial and tissue oxygen tensions, producing a wide variety of physiological effects at the cellular and sub cellular level. Some of these effects have been postulated to be beneficial in the context of ischemic stroke. Most of the recovery after stroke occurs in the first 30 to 90 days after the acute event. Recovery is largely based on recovery of brain that is injured, but viable. Physiological imaging studies (PET, EEG) have demonstrated that brain tissue may remain alive but not functional for months or years after ischemic insult. Subjects will be selected from the stroke population based on an expectation that they would experience a clinically significant improvement. Eligible subjects will have suffered an ischemic stroke involving the cerebral cortex within the last 6 to 36 months. The study will be enrolling 140 subjects and will be randomized to two different treatment arms: experimental group and a waitlist group. Each subject will receive a series of forty 2 hour treatments, delivered once a day, 5 days a week, within the hyperbaric oxygen chamber.There will be assessments completed before treatment series begins, 3 weeks and 6 weeks into treatment and then again at the end of treatment. After treatment ends, the investigators will conduct these assessments again at 3 months, 6 months, 9 months and 1 year from the date of the participants last treatment.
Interventions
OTHERHyperbaric Oxygen
The only intervention given will be 100% oxygen under hyperbaric pressure.
Sponsors
University of British Columbia
Study design
Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
1. Age between 19 and 85. 2. Able to speak English and give informed consent or have a substitute decision maker and able to assent. 3. One or more ischemic stroke(s) involving the cerebral cortex or cerebellum within the last 6 to 36 months 4. Able to sit in the chamber with the assistance of a waist and chest strap for 120 minutes.
Exclusion criteria
1. Contraindication to HBOT (Appendix C) including: 1. Untreated collapsed lung (pneumothorax) 2. Have taken the chemotherapy drug Doxorubicin within 72 hours 3. Have taken the chemotherapy drug Bleomycin within 4 months 4. Bowel obstruction 5. Heart pacemaker of unknown make and model 6. Pregnancy 7. Cigarette Smoking 8. Chronic Obstructive Pulmonary Disease (COPD) 2. Participation in other stroke related studies. 3. Previous history stroke \> 36 months prior to study baseline
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in the Stroke Impact Scale (SIS-16) from baseline over the duration of the study | Pre treatment (Baseline and after waiting period is completed), During Treatment (3 weeks, 6 weeks) and Post Treatment (9 weeks post baseline, 8 months post and 14 months) |
Secondary
| Measure | Time frame |
|---|---|
| Digital Symbol Substitution Test | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
| Berg Balance Test | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
| 6 metre walk test | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
| 6 minutes walk test | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
| National Institute of Health Stroke Scale (NIHSS) | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
| Trail Making Test | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
| Grip Strength | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
| Centre for Epidemiologic Studies Depression Scale (CESD) | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
| Medical Outcomes Study Short Form (SF-36) | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
| Montreal Cognitive Assessment (MoCA) | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
| Health Economics Questionnaire | Pre treatment (Baseline and after waiting period) and Post Treatment (5 months, 8 months, 11 months and 14 months) |
| Nine hole peg board | Pre treatment (Baseline and after waiting period) and Post Treatment (9 weeks post baseline, 8 months post and 14 months post) |
Countries
Canada
Outcome results
None listed