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Tailored exercise shows promise for spinal cord injury recovery

NCT ID NCT06259227

Symptom relief Sponsor: Sint Maartenskliniek Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early This study
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether personalized fitness training could improve heart and lung fitness in people with incomplete spinal cord injury during early rehabilitation. Nineteen participants were assigned to either personalized training sessions or usual care for six weeks. The study was terminated early, so results are limited.

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

19 people

The number who actually took part.

Started

Jan 2024

Finished

Aug 2025

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Diagnosis of incomplete spinal cord injury based on a stable cause (e.g. traumatic) * Spinal cord injury classification C or D on the American Spinal Injury Association (ASIA) impairment scale * During this study in the subacute phase (\< 6 months post injury) * Hospitalized in the Sint Maartenskliniek for a primary, inpatient rehabilitation program * Older than 18 years of age * Able to understand and perform study related procedures * Capable to sit at least 3 times a day for 2 hours (prerequisites to start the active rehabilitation program) * The ability to use an arm ergometer Exclusion Criteria: * Unable to give informed consent * Language barrier * Participating in another interventional study targeting cardiorespiratory fitness * Have contraindications to perform exercise during the rehabilitation program

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Conditions

The condition(s) this trial relates to.

spinal cord injury

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Exercise training Incomplete spinal cord injury

Contacts and locations

Locations

  • Sint Maartenskliniek

    Ubbergen, 6574 NA, Netherlands

More trials for these conditions

Other studies related to the condition(s) this trial covers.