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Magnetic Resonance Imaging of Cognitive Deficits in the Brain of Individuals With Spinal Cord Injury

Magnetic Resonance Imaging of Cognitive Deficits in the Brain of Individuals With Spinal Cord Injury

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06309888
Acronym
SCI_Cog
Enrollment
54
Registered
2024-03-13
Start date
2024-02-01
Completion date
2024-11-18
Last updated
2025-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Injury

Keywords

spinal cord injury, neuroimaging, cognition, executive functions

Brief summary

In the case of spinal cord injury, rehabilitation is particularly focused on motor skills. Non-motor impairments such as thinking difficulties did not receive a lot of attention to date. In this research project, the investigators want to find out how thinking difficulties become noticeable in the brain with spinal cord injury. Participation procedure: Participants who take part will be asked to come to an examination once. The duration of the examination is between 2 and 2.5 hours (including around 55 minutes in the magnetic resonance imaging scanner, including preparation and follow-up).

Interventions

None listed

Sponsors

Swiss Paraplegic Research, Nottwil
Lead SponsorNETWORK

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

(with and without spinal cord injury): * Male or Female * Age between 18 and 60 * German native speaker * Normal or corrected-to-normal visual acuity Additional inclusion criteria (spinal cord injury only): * A diagnosis of traumatic spinal cord injury (SCI) * Time since injury 12 months or longer * American Spinal Injury Association Impairment Scale (AIS) grade A, B, C and D

Exclusion criteria

(with and without spinal cord injury): * Contraindication for magnetic resonance imaging examinations (e.g., cardiac pacemaker etc.) * Pregnancy * Diagnosis of other psychiatric or neurological disorders (including tumor in the central nervous system) * Alcohol and/or drug abuse * Confirmed diagnosis of traumatic brain injury * Insufficient hand function (not able to hold a pen due to the restricted motor abilities)

Design outcomes

Primary

MeasureTime frameDescription
Brain activityBaselineBrain activity defined as changes in oxygen levels in the blood during the execution of cognitive tasks on cognitive inhibition and verbal fluency (executive functions), and at rest

Secondary

MeasureTime frameDescription
Brain morphometryBaselineVolume of brain structures in cubic millimetres
Level of life satisfactionBaselineSatisfaction with Life Scale (validated questionnaire assessing life satisfaction)
Level of anxietyBaselineState-Trait Anxiety Inventory (validated questionnaire assessing anxiety)
Level of painBaselineValidated questionnaire assessing pain severity
Behavioral performanceBaselineAccuracy on cognitive inhibition task (in percentage)
Level of attention and awarenessBaselineMindful Attention and Awareness scale (validated questionnaire assessing level of attention and awareness)
Motor symptom severityBaselineMotor symptoms severity (from level A to E) based on the International Standards for Neurological Classification of spinal cord injury (ISNCSCI)
DemographicsBaselineDemographic information such as age, sex and education level, as well as time since injury
Quality of sleepBaselinePittsburgh Sleep Quality Index (validated questionnaire assessing sleep quality)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026