TY - JOUR
T1 - Brain stimulation for arm recovery after stroke (B-STARS)
T2 - protocol for a randomised controlled trial in subacute stroke patients
AU - van Lieshout, Eline C.C.
AU - Visser-Meily, Johanna M.A.
AU - Neggers, Sebastiaan F.W.
AU - van der Worp, H. Bart
AU - Dijkhuizen, Rick M.
N1 - Funding Information:
Funding This work was supported by the Netherlands Organization for Scientific Research(VICI 016.130.662).
Publisher Copyright:
© 2017 Article author(s). All rights reserved.
PY - 2017/8/1
Y1 - 2017/8/1
N2 - Introduction: Many patients with stroke have moderate to severe long-term sensorimotor impairments, often including inability to execute movements of the affected arm or hand. Limited recovery from stroke may be partly caused by imbalanced interaction between the cerebral hemispheres, with reduced excitability of the ipsilesional motor cortex while excitability of the contralesional motor cortex is increased. Non-invasive brain stimulation with inhibitory repetitive transcranial magnetic stimulation (rTMS) of the contralesional hemisphere may aid in relieving a post-stroke interhemispheric excitability imbalance, which could improve functional recovery. There are encouraging effects of theta burst stimulation (TBS), a form of TMS, in patients with chronic stroke, but evidence on efficacy and long-term effects on arm function of contralesional TBS in patients with subacute hemiparetic stroke is lacking. Methods and analysis: In a randomised clinical trial, we will assign 60 patients with a first-ever ischaemic stroke in the previous 7-14 days and a persistent paresis of one arm to 10 sessions of real stimulation with TBS of the contralesional primary motor cortex or to sham stimulation over a period of 2 weeks. Both types of stimulation will be followed by upper limb training. A subset of patients will undergo five MRI sessions to assess post-stroke brain reorganisation. The primary outcome measure will be the upper limb function score, assessed from grasp, grip, pinch and gross movements in the action research arm test, measured at 3 months after stroke. Patients will be blinded to treatment allocation. The primary outcome at 3 months will also be assessed in a blinded fashion. Ethics and dissemination: The study has been approved by the Medical Research Ethics Committee of the University Medical Center Utrecht, The Netherlands. The results will be disseminated through (open access) peer-reviewed publications, networks of scientists, professionals and the public, and presented at conferences.
AB - Introduction: Many patients with stroke have moderate to severe long-term sensorimotor impairments, often including inability to execute movements of the affected arm or hand. Limited recovery from stroke may be partly caused by imbalanced interaction between the cerebral hemispheres, with reduced excitability of the ipsilesional motor cortex while excitability of the contralesional motor cortex is increased. Non-invasive brain stimulation with inhibitory repetitive transcranial magnetic stimulation (rTMS) of the contralesional hemisphere may aid in relieving a post-stroke interhemispheric excitability imbalance, which could improve functional recovery. There are encouraging effects of theta burst stimulation (TBS), a form of TMS, in patients with chronic stroke, but evidence on efficacy and long-term effects on arm function of contralesional TBS in patients with subacute hemiparetic stroke is lacking. Methods and analysis: In a randomised clinical trial, we will assign 60 patients with a first-ever ischaemic stroke in the previous 7-14 days and a persistent paresis of one arm to 10 sessions of real stimulation with TBS of the contralesional primary motor cortex or to sham stimulation over a period of 2 weeks. Both types of stimulation will be followed by upper limb training. A subset of patients will undergo five MRI sessions to assess post-stroke brain reorganisation. The primary outcome measure will be the upper limb function score, assessed from grasp, grip, pinch and gross movements in the action research arm test, measured at 3 months after stroke. Patients will be blinded to treatment allocation. The primary outcome at 3 months will also be assessed in a blinded fashion. Ethics and dissemination: The study has been approved by the Medical Research Ethics Committee of the University Medical Center Utrecht, The Netherlands. The results will be disseminated through (open access) peer-reviewed publications, networks of scientists, professionals and the public, and presented at conferences.
KW - arm
KW - brain stimulation
KW - clinical trial
KW - intervention
KW - rehabilitation
KW - repetitive transcranial magnetic stimulation
KW - stroke
KW - Stroke Rehabilitation/methods
KW - Humans
KW - Middle Aged
KW - Male
KW - Recovery of Function
KW - Transcranial Magnetic Stimulation
KW - Young Adult
KW - Aged, 80 and over
KW - Adult
KW - Female
KW - Upper Extremity
KW - Hand Strength
KW - Stroke/complications
KW - Movement
KW - Brain/physiopathology
KW - Adolescent
KW - Aged
KW - Paresis/etiology
KW - Research Design
UR - http://www.scopus.com/inward/record.url?scp=85046987632&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2017-016566
DO - 10.1136/bmjopen-2017-016566
M3 - Article
C2 - 28851789
AN - SCOPUS:85046987632
SN - 2044-6055
VL - 7
SP - e016566
JO - BMJ Open
JF - BMJ Open
IS - 8
M1 - e016566
ER -