Spinal Cord Injury Clinical Trial
— SCI_CogOfficial title:
Magnetic Resonance Imaging of Cognitive Deficits in the Brain of Individuals With Spinal Cord Injury
NCT number | NCT06309888 |
Other study ID # | 2023-18 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | February 1, 2024 |
Est. completion date | December 2026 |
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).
Status | Recruiting |
Enrollment | 60 |
Est. completion date | December 2026 |
Est. primary completion date | December 2026 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | 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) |
Country | Name | City | State |
---|---|---|---|
Switzerland | Swiss Paraplegic Research | Nottwil | Lucerne |
Lead Sponsor | Collaborator |
---|---|
Swiss Paraplegic Research, Nottwil |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Brain activity | Brain 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 | Baseline | |
Secondary | Behavioral performance | Accuracy on cognitive inhibition task (in percentage) | Baseline | |
Secondary | Behavioral performance | Reaction time (in milliseconds) on cognitive inhibition task | Baseline | |
Secondary | Behavioral performance | Number of errors on cognitive inhibition task | Baseline | |
Secondary | Behavioral performance | Number of correct words on verbal fluency task | Baseline | |
Secondary | Behavioral performance | Number of mistakes on verbal fluency task | Baseline | |
Secondary | Brain morphometry | Volume of brain structures in cubic millimetres | Baseline | |
Secondary | Level of life satisfaction | Satisfaction with Life Scale (validated questionnaire assessing life satisfaction) | Baseline | |
Secondary | Level of anxiety | State-Trait Anxiety Inventory (validated questionnaire assessing anxiety) | Baseline | |
Secondary | Level of pain | Validated questionnaire assessing pain severity | Baseline | |
Secondary | Quality of sleep | Pittsburgh Sleep Quality Index (validated questionnaire assessing sleep quality) | Baseline | |
Secondary | Level of attention and awareness | Mindful Attention and Awareness scale (validated questionnaire assessing level of attention and awareness) | Baseline | |
Secondary | Motor symptom severity | Motor symptoms severity (from level A to E) based on the International Standards for Neurological Classification of spinal cord injury (ISNCSCI) | Baseline | |
Secondary | Demographics | Demographic information such as age, sex and education level, as well as time since injury | Baseline |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT02574572 -
Autologous Mesenchymal Stem Cells Transplantation in Cervical Chronic and Complete Spinal Cord Injury
|
Phase 1 | |
Recruiting |
NCT05941819 -
ARC Therapy to Restore Hemodynamic Stability and Trunk Control in People With Spinal Cord Injury
|
N/A | |
Completed |
NCT05265377 -
Safety and Usability of the STELO Exoskeleton in People With Acquired Brain Injury and Spinal Cord Injury
|
N/A | |
Recruiting |
NCT02331979 -
Improving Bladder Function in SCI by Neuromodulation
|
N/A | |
Completed |
NCT02777281 -
Safe and Effective Shoulder Exercise Training in Manual Wheelchair Users With SCI
|
N/A | |
Recruiting |
NCT02978638 -
Electrical Stimulation for Continence After Spinal Cord Injury
|
N/A | |
Completed |
NCT02161913 -
Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers
|
N/A | |
Withdrawn |
NCT02237547 -
Safety and Feasibility Study of Cell Therapy in Treatment of Spinal Cord Injury
|
Phase 1/Phase 2 | |
Completed |
NCT02262234 -
Education Interventions for Self-Management of Pain Post-SCI: A Pilot Study
|
Phase 1/Phase 2 | |
Completed |
NCT01642901 -
Zoledronic Acid in Acute Spinal Cord Injury
|
Phase 3 | |
Completed |
NCT01884662 -
Virtual Walking for Neuropathic Pain in Spinal Cord Injury
|
N/A | |
Terminated |
NCT02080039 -
Electrical Stimulation of Denervated Muscles After Spinal Cord Injury
|
N/A | |
Completed |
NCT01471613 -
Lithium, Cord Blood Cells and the Combination in the Treatment of Acute & Sub-acute Spinal Cord Injury
|
Phase 1/Phase 2 | |
Terminated |
NCT01433159 -
Comparison of HP011-101 to Standard Care for Stage I-II Pressure Ulcers in Subjects With Spinal Cord Injury
|
Phase 2 | |
Completed |
NCT02149511 -
Longitudinal Morphometric Changes Following SCI
|
||
Completed |
NCT01467817 -
Obesity/Overweight in Persons With Early and Chronic Spinal Cord Injury (SCI)
|
N/A | |
Completed |
NCT00663663 -
Telephone Intervention for Pain Study (TIPS)
|
N/A | |
Terminated |
NCT01005615 -
Patterned Functional Electrical Stimulation (FES) Ergometry of Arm and Shoulder in Individuals With Spinal Cord Injury
|
Phase 1/Phase 2 | |
Completed |
NCT01025609 -
Dietary Patterns and Cardiovascular (CVD) Risk in Spinal Cord Injury (SCI) Factors In Individuals With Chronic Spinal Cord Injury
|
||
Completed |
NCT01086930 -
Early Intensive Hand Rehabilitation After Spinal Cord Injury
|
Phase 3 |