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Spinal injury study probes the Brain's sense of self

NCT ID NCT06688916

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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 Results may not be published yet.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
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This status has not been confirmed recently, so it may be out of date.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 looks at how spinal cord injury (SCI) affects a person's sense of their own body, known as embodiment. Researchers will use questionnaires and brain scans (fMRI) to compare 80 people with and without SCI. The goal is to understand why some people with SCI feel disconnected from their body and how this affects daily life.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this study could reveal how spinal cord injury alters body awareness, potentially guiding future rehabilitation strategies.
What could go wrong
This is an observational study, not a treatment trial. It will not directly improve symptoms or provide a therapy.

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.

Participants

About 80 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2025

Expected to finish

May 2026

An estimate. End dates often move.

Lead sponsor

A research network

The lead sponsor is a research network or cooperative group.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Individuals with spinal cord injury and healthy controls.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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 for all participants: * Age between 18 and 60 * Normal or corrected-to-normal visual acuity * German or Italian native speaker Additional Inclusion Criteria only for individuals with SCI: * Diagnosis of traumatic spinal cord injury * Lesion level below T1 (first thoracic vertebra) * Time since injury \>= 12 months * Residual sensation on the upper leg (sensory capability of 1 or higher on at least one leg in the dermatomes L2 and L3 for both light touch and pin prick). Exclusion Criteria for all participants: * Pregnancy or breastfeeding * Diagnosis of other psychiatric or neurological disorders (e.g. epilepsy, tumor in the central nervous system) * Confirmed diagnosis of alcohol and/or drug abuse with active consumption within the last 6 months * Confirmed diagnosis of traumatic brain injury, intended as visible changes in the brain diagnosed by a radiologist * Stroke * Inability to perform study procedures (e.g. inability to consent) Additional Exclusion Criteria for both HC and SCI undergoing the fMRI procedure: * Active medical devices (e.g. cardiac pacemaker) * Inability to perform study procedures (e.g. claustrophobia)

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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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Swiss Paraplegic Research

    RECRUITING

    Nottwil, Canton of Lucerne, 6207, Switzerland

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