Arm workouts may boost heart function after spinal cord injury — a trial puts it to the test
NCT ID NCT07725952
First seen Jul 24, 2026 · Last updated Sep 04, 2026 · Updated 2 times
Summary
This trial tests whether an 8-week upper-limb resistance training program can improve cardiovascular autonomic function in adults with chronic spinal cord injury. Participants are randomly assigned to either supervised arm exercises three times per week or a control group. Researchers will measure heart rate variability, baroreflex sensitivity, blood pressure changes, and quality of life to see if strength training helps regulate heart function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a supervised upper-limb resistance training program
- What this could lead to
- If it works, this could point toward a simple exercise program to improve cardiovascular health and reduce dizziness in people with spinal cord injury.
- What could go wrong
- This is a small, early-stage trial with only 20 participants, so results may not apply widely. The training requires consistent effort, and benefits may vary.
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
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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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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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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19 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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.
Inclusion Criteria: * Provided written informed consent and agreed to participate in the study. * Adults aged 19 to 85 years. * Chronic spinal cord injury (SCI) of traumatic or non-traumatic etiology, at least 6 months after injury. * Cervical or thoracic spinal cord injury. * Classified as American Spinal Injury Association (ASIA) Impairment Scale (AIS) grade A, B, C, or D. * Sufficient upper-limb range of motion to perform resistance training. * Elbow extensor muscle strength of Manual Muscle Test (MMT) grade 3 or higher. Exclusion Criteria: * Presence of any serious medical condition that would preclude participation in the study. * Inability to understand or perform the exercise program. * Uncontrolled diabetes mellitus or progressive neurological disease. * Uncontrolled hypertension (systolic blood pressure \>140 mmHg or diastolic blood pressure \>90 mmHg). * History of cardiovascular disease within the past 6 months. * Current use of medications that may affect heart rate variability (HRV) or baroreflex sensitivity (BRS). * Severe orthostatic hypotension (OH) or autonomic dysreflexia (AD). * Considered unsuitable for participation in the study by a board-certified specialist in Physical and Rehabilitation Medicine.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Pusan National University Yangsan Hospital
Yangsan, Gyeongsangnam-do, 50612, South Korea
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Determination of efficacy of sustained motor contraction generated using StimWave peripheral nerve stimulator
- Can magnetic pulses to the brain restore hand control after spinal injury?
- Robotic legs may help rebuild bone in people with spinal cord injury
- Could a muscle hormone shield bones after spinal cord injury?
- Can hope and trust boost engagement with rehab robots?
- Spinal zaps may calm muscle spasms after injury