AI helps paralyzed patients walk better in real time
NCT ID NCT07452133
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new AI system that adjusts electrical stimulation to the spine in real time while people with spinal cord injury walk. The goal is to improve muscle activation and walking ability compared to standard stimulation. The study involves 7 participants and focuses on safety and feasibility.
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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 7 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2028
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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21 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.
Inclusion Criteria: Healthy volunteers: 1. Adults aged 21 years or older with the mental capacity to provide informed consent. 2. No prior diagnosis of neuromuscular or neurological conditions affecting the lower limbs. 3. Able to walk independently with a normal gait pattern, as confirmed by clinical observation done by the study team. SCI patients: 1. Age 21 -75 years; 2. Non-progressive, incomplete SCI (traumatic or non-traumatic). 3. International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) /ASIA Impairment scale (AIS) grade B, C, or D, with Lower Extremity Motor Scores (ISNCSCI-LEMS) less than or equal to 40; 4. Injury level at/above L1 (above conus medullaris) with intact segmental reflexes below level of lesion; 5. Able to provide informed consent; 6. No contraindication for tSCS, such as pace makers or other implantable electrical devices; 7. Eligible for body-weight support treadmill training; 8. Able to stand with body weight support and/or assistance. Exclusion Criteria: Healthy voluteers: 1. Presence of significant or unstable medical comorbidities, including uncontrolled cardiopulmonary disease or severe cognitive impairment, as determined by the study team. 2. Diagnosis of any neuromuscular or musculoskeletal disorders (e.g., congenital skeletal deformity, limb amputation, neurological disorders, myopathy). 3. Abnormal gait pattern due to underlying medical co-morbidities, as identified through physical examination and clinical assessment, and confirmed by the study team. 4. Current pregnancy. SCI patients: 1. Significant or unstable medical co-morbidities, including uncontrolled cardiopulmonary disease, severe cognitive impairment, or severe dysautonomia, as determined by the study team; 2. Uncontrolled neuropathic or musculoskeletal pain, or contractures affecting participation in therapy; 3. Known history of peripheral nerve injury (e.g., traumatic nerve injury, entrapment neuropathy); 4. Pregnancy; 5. Active malignancy or ongoing cancer treatment; 6. Skin conditions (e.g., ulcers, infections, malignant lesions) that limit the application of tSCS electrodes; 7. Prior exposure to tSCS or eSCS interventions.
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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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Singapore General Hospital
Singapore, Singapore
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Other studies related to the condition(s) this trial covers.
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