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PAS for Lower Extremity Rehabilitation in Tetraplegic Patients

Long-term Paired Associative Stimulation for Rehabilitation of Lower Extremities in Persons With Incomplete Tetraplegia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03459885
Enrollment
5
Registered
2018-03-09
Start date
2018-02-28
Completion date
2019-06-28
Last updated
2025-05-13

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

Conditions

Spinal Cord Diseases, Spinal Cord Injuries

Brief summary

The investigators have recently shown in incomplete SCI patients that long-term paired associative stimulation is capable of restoring voluntary control over some paralyzed muscles and enhancing motor output in the weak muscles (1,2). In this study, the investigators will administer long-term paired associative stimulation to patients with incomplete cervical level SCI and investigate its effectiveness for lower extremity rehabilitation.

Interventions

DEVICEPaired associative stimulation (with eXimia magnetic stimulator and Dantec Keypoint® electroneuromyography device)

Paired associative stimulation (PAS) administered several times per week for 8 weeks to lower limbs. PAS comprises transcranial magnetic stimulation (eXimia magnetic stimulator, Nexstim Ltd, Helsinki, Finland) and peripheral nerve stimulation (given with Dantec Keypoint® electroneuromyography device (Natus Medical Incorporated, Pleasanton, CA, USA)).

Sponsors

Validia Rehabilitation Centre
CollaboratorUNKNOWN
Helsinki University Central Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* cervical incomplete SCI

Exclusion criteria

* epilepsy * metal inclusion in the head area * pacemaker * hearing device * high intracranial pressure

Design outcomes

Primary

MeasureTime frameDescription
Daniels and Worthingham's Muscle Testing2 days after the last stimulation sessionLeg muscle stenght is evaluated on 0-5 scale (0=no movement, 5=normal)

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026