Tremor occurs in up to 55% of dystonia patients, which is known as dystonic tremor syndrome (DTS). Tremor can be present in the body part affected by dystonia (dystonic tremor, DT), or an unaffected body part (tremor associated with dystonia, TAWD). DTS can be treated with botulinum neurotoxin (BoNT) injections, but BoNT is effective in only about 60-70% of patients. It is unknown which patients benefit most from BoNT treatment. The investigators aim to explore the associations between clinical and pathophysiological tremor characteristics and BoNT efficacy. To do so, the investigatorswill measure clinical, electrophysiological, ultrasonographic and (functional) magnetic resonance imaging ((f)MRI) characteristics before the start of BoNT treatment and measure BoNT efficacy after three three-monthly BoNT sessions.
Rationale: Tremor occurs in up to 55% of dystonia patients, which is known as dystonic tremor syndrome (DTS). Tremor can be present in the body part affected by dystonia (dystonic tremor, DT), or an unaffected body part (tremor associated with dystonia, TAWD). DTS can be treated with botulinum neurotoxin (BoNT) injections, but BoNT is effective in only about 60-70% of patients. It is unknown which patients benefit from BoNT treatment. This highlights the need for personalized treatment. Objective: The primary objective is to explore the associations between clinical, electrophysiological, ultrasonographic and (functional) magnetic resonance imaging ((f)MRI) tremor characteristics and BoNT efficacy in DTS of the upper extremity. The secondary objectives are to: * Explore the clinical, electrophysiological, ultrasonographic and (f)MRI differences between DT and TAWD of the upper extremity. * Explore the agreement between a clinical assessment, polymyography (PMG) and muscle ultrasound (MUS) on muscle selection in DTS of the upper extremity. Study design: An uncontrolled multi-centre low-intervention clinical trial where subjects participate for ± 8 months Study population: 60 adults with DTS (± 30 DT/ 30 TAWD) of the upper extremity who start 12-weekly BoNT treatment in normal clinical practice. Main study parameters/endpoints: the associations between clinical, electrophysiological, ultrasonographic, and (f)MRI tremor characteristics at baseline and BoNT efficacy (change in TRG Essential Tremor Rating Assessment Scale (TETRAS) from baseline to 28 weeks). Secondary trial endpoints: * The clinical, electrophysiological, ultrasonographic and (f)MRI differences between DT and TAWD at baseline. * The agreement between a clinical assessment, PMG and MUS on muscle selection. Intervention: Participants are treated with three consecutive BoNT sessions in normal clinical practice. Participants will undergo additional diagnostic procedures: 2 clinical assessments, 2 PMGs, 1 MUS recordings and 1 fMRI assessment and will fill in 2 questionnaires before and after the BoNT sessions.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
60
We will measure muscle activity using surface electromyography and tremor using inertial measurement units while subjects perform rest, posturing and kinetic tasks.
We will obtain B-mode images and videos of upper extremity muscles of the most affected upper extremity.
Subjects will undergo (f)MRI scanning involving concurrent electromyography, accelerometry and functional magnetic resonance imaging.
We will assess tremor and dystonia severity using clinical scales.
We will collect patient-reported outcomes.
Three consequetive botulinum toxin injections of the upper extremities
Donders Centre for Cognitive Neuroimaging
Nijmegen, Gelderland, Netherlands
RECRUITINGRadboud University Medical Center
Nijmegen, Gelderland, Netherlands
RECRUITINGCanisius-Wilhelmina Ziekenhuis
Nijmegen, Gelderland, Netherlands
RECRUITINGTremor severity assessed by the TRG Essential Tremor Rating Assessment Scale (TETRAS)
The primary outcome is the clinical tremor severity measured by the TRG Essential Tremor Rating Assessment Scale (TETRAS) at 28 weeks. The scale ranges between 0 and 112 points, with higher scores indicating a more severe tremor. The TETRAS consists of two subcategories: a 12-item activities of daily living subscale and a 9-item performance scale. The daily living subscale is scored by interviewing the participant. The performance scale is rated by observing the participants while they are performing multiple tasks.
Time frame: Baseline, 28 weeks
Tremor severity assessed by the Fahn-Tolosa-Marin Tremor Rating Scale (FTM-TRS)
FTM-TRS \[0-152\]: higher scores indicate a more severe tremor.
Time frame: Baseline, 28 weeks
Dystonia severity assessed by the Burke-Fahn-Marsden Dystonia Rating Scale (BFM-DRS)
BFM-DRS \[0-150\]: higher scores indicate more severe dystonia.
Time frame: Baseline, 28 weeks
Additional neurological signs assessed by the Standardised Tremor Elements Assessment (STEA)
STEA \[0-27\]: higher scores make a diagnosis of dystonic tremor syndrome instead of essential tremor more likely.
Time frame: Baseline
Quality of life assessed by the Quality of Life Essential Tremor Questionnaire (QUEST)
QUEST \[0-120\]: higher scores indicate greater dissatisfaction.
Time frame: Baseline, 28 weeks
Psychological stress assessed by the Perceived stress scale (PSS)
PSS \[0-4\]: higher scores indicate higher levels of perceived stress
Time frame: Baseline, 28 weeks
Pain assessed by the Numeric Pain Rating Scale (NPRS)
NPRS \[0-10\]: 0 indicates no pain and 10 the worst imaginable pain
Time frame: Baseline, 28 weeks
Patient-reported change in tremor severity assessed by the Patient Global Impression of Change (PGIC)
PGIC \[-3: much worse, -2: moderately worse, -1: slightly worse, 0: no change, 1: slightly better, 2: moderately better, 3: much better\]
Time frame: 28 weeks
Electrophysiological characteristics
e.g. tremor power, dominant frequency, frequency-width at half-width power, intermuscular coherence, tremulous muscles
Time frame: Baseline, 28 weeks
Ultrasonographic tremulous activity
Time frame: Baseline
Tremor related cerebral activity
Quantified using functional MRI scanning
Time frame: Baseline
Botulinum toxin parameters
e.g. injection schemes, rationale for muscle selection, adherence
Time frame: Baseline, 12 and 24 weeks
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