Blood pressure cuff trick may boost hand function in paralysis
NCT ID NCT03851302
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This small study tested whether briefly restricting blood flow to one arm (called remote ischemic conditioning, or RIC) could improve hand function in people with spinal cord injury or ALS. Participants did hand exercises while receiving either active RIC or a sham version. The goal was to see if RIC could boost nerve signals and reduce inflammation. The study included 21 people and measured changes in muscle responses and blood markers.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- remote ischemic conditioning (brief blood-flow restriction using a blood pressure cuff)
- What this could lead to
- If this approach works, it could point toward a simple, low-cost way to boost hand function during rehabilitation for people with spinal cord injury or ALS.
- What could go wrong
- This is a very small, early-stage study with only 21 participants. The results may not apply to everyone, and the effects might be too small to make a real difference in daily life.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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21 people
The number who actually took part.
- Started
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Oct 2019
- Finished
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Oct 2022
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Able-bodied participants 1. Age between 18 and 75 years; 2. No known central or peripheral neurological disease or injury. SCI participants Inclusion Criteria: 1. Age between 18 and 75 years; 2. Chronic (more than 12 months since injury) motor-incomplete SCI between neurological levels C2-C8 3. Detectable F-wave responses of the left or right abductor pollicis brevis (APB) to median nerve stimulation; 4. Detectable motor evoked potentials in left or right APB muscles to transcranial magnetic stimulation; 5. Able to perform thumb-middle finger opposition pinch task with detectable APB EMG muscle activity. ALS participants 1. Age between 21 and 75 years; 2. Diagnosis of probable or definite ALS. 3. Incomplete weakness of left or right wrist or hand muscles: score of 2, 3, or 4 (out of 5) on manual muscle testing of finger extension, finger flexion, or finger abduction. 4. Detectable motor evoked potentials in left or right APB muscles to transcranial magnetic stimulation; 5. Able to perform thumb-middle finger opposition pinch task with detectable APB electromyography (EMG) muscle activity. Exclusion Criteria: 1. Multiple spinal cord lesions; 2. History of seizures; 3. Use of medications that significantly lower seizure threshold, such as amphetamines and bupropion; 4. History of implanted brain/spine/nerve stimulators, aneurysm clips, or cardiac pacemaker/defibrillator; 5. Any extremity soft tissue, orthopedic, or vascular condition or injury that may contraindicate remote limb ischemic conditioning (RLIC) (uncontrolled hypertension, peripheral vascular disease, hematological disease, severe hepatic or renal dysfunction); 6. Any other contraindication to undergoing magnetic resonance imaging (except for claustrophobia); 7. Clinically significant infection of any kind (urinary tract, pulmonary, skin or other) 8. Significant coronary artery or cardiac conduction disease; 9. Open skin lesions over the neck, shoulders, or arms; 10. Pregnancy 11. Unsuitable for study participation as determined by study physician. In addition, a medical record review will be conducted to identify any other medical concerns that might increase the risks associated with participation.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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James J. Peters VA Medical Center
The Bronx, New York, 10468, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Serotonin precursor probed for spinal cord injury effects
- Breathing device tested to slow lung decline in ALS
- Can hospital codes reliably track home ventilation in ALS?
- Breathing brief Low-Oxygen bursts may boost sleep apnea treatment
- Pure oxygen tested as a switch for dormant nerves after spinal cord injury
- Spinal stimulation tested to help kids with spinal cord injuries sit taller