Skip to content

Brain-STimulation for Arm Recovery after Stroke

Brain-STimulation for Arm Recovery after Stroke - B-STARS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON50466
Enrollment
60
Registered
2016-10-19
Start date
2017-04-14
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

cerebrovascular accident Stroke

Interventions

Contralesional cTBS over the hand area of the primary motor cortex on a daily basis for 2 weeks (except the weekends). Sham stimulation will be done with a reverse coil orientation.

Sponsors

Divisie Beeld
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) Adult patient age * 18; 2) first-ever unilateral ischemic and hemorrhagic stroke (i.e., within the cerebral hemispheres, brainstem); 3) paresis of one arm, with a SA score shoulder abduction *9 (Motricity Index); 4) within the first 3 weeks after stroke onset; 5) signed informed consent.

Exclusion criteria

Exclusion criteria: 1) Disabling medical history (severe or recent heart disease, severe head trauma, coercively treated at a psychiatric ward); 2) history of epilepsy; 3) Normal to almost normal use of hand; maximum Motricity Index hand score (score of 33) 4) severe deficits in communication, memory, or understanding that impede proper study participation, as determined by the treating physician; 5) contraindications for TMS (e.g. metal (implants) in skull/scalp/head or fragments from welding or metalwork, implanted device, pregnancy). N.B. metal fillings (i.e. conductive) or non-ferromagnetic dental implants are an exception to the rule.

Design outcomes

Primary

MeasureTime frame
Performance on an upper limb function test of the paretic arm.

Secondary

MeasureTime frame
Performance on additional upper limb function tests, tests on disability and quality of life and neural network reorganisation. Optional are the MRI scans and a single interview.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)