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Clinical Trials/NCT04611009
NCT04611009RecruitingPhase 2

Treatment Effect and Relevance on Daily Life of a Video-supervised Sensorimotor Training Program and Its Influence on the Pathophysiology in Writer's Cramp

University Hospital Schleswig-Holstein2 sites in 1 country54 target enrollmentStarted: June 26, 2020Last updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Recruiting
Sponsor
Enrollment
54
Locations
2
Primary Endpoint
Canadian Occupational Performance Measure

Study Overview

Brief Summary

Writer's cramp is the most common task-specific dystonia. It is characterized by involuntary co-contraction of antagonistic muscles during writing. This disabling condition may force patients to give up their occupation. In this study the efficacy of a twelve months long-term training in patients with writer's cramp will be investigated. Two different programs will be offered: The first one will consist of a sensorimotor, the second one of an awareness training. All patients will benefit from video-based supervision with the aim to establish a practice-oriented therapeutic approach that will be available to all patients independently of their home location. The treatment effect will be measured primary with the patient-centered Canadian Occupational Performance Measure (COPM) and secondary with clinical scales to assess the clinical efficacy and everyday constraints. Writing will be assessed with a computer-based kinematic writing analysis. To evaluate the influence on the brain network, several functional magnetic resonance imaging (fMRI) evaluations will be performed. This project is of minimal risk without negative side effects from the training. The risks for the MRI experiment are equal to a non-contrast standard MRI investigation.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Masking Description

Participants are blinded towards their participation in the two arms Clinical scales, kinematic writing anlysis and functional MRI will be analyzed by persons, who are blinded to the type of training group allocation

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Right handed idiopathic WC according to standardized criteria (simple and complex WC, any dystonic posture (including flexion, extension, pronation, supination))
  • able to participate in video-calls

Exclusion Criteria

  • Additional neurological or psychiatric diseases
  • left-handed patients
  • last botulinum toxin treatment <3 months, remaining weakness from the last injection
  • concomitant use of anticholinergics or sedating medication
  • Exclusion criteria for MRI:
  • Cardiac pacemaker, electronic or metal implants
  • pregnancy or suspected pregnancy
  • severe ametropia, anxiety in small rooms

Outcomes

Primary Outcomes

Canadian Occupational Performance Measure

Time Frame: Change from baseline to month 4, 8, 12

The Canadian Occupational Performance Measure will serve as the primary outcome measure. Patients grade their self-perceived performance and satisfaction of writing related occupations in daily life in respect to the goals they had identified and prioritized. The COPM ist patient centered end reflects the real life of the participants.

Secondary Outcomes

  • Writer's Cramp Rating Scale(Change from baseline to month 4, 8, 12)
  • kinematic writing analysis(Change from baseline to month 4, 8, 12)
  • writing during functional magnetic resonance imaging (fMRI)(Change from baseline to month 4, 8, 12)
  • qualitative interviews(Change from baseline to month 4, 12)
  • Arm Dystonia Disability Scale(Change from baseline to month 4, 8, 12)
  • Serial Reaction Time Task during functional magnetic resonance imaging (fMRI)(Change from baseline to month 4, 8, 12)

Investigators

Sponsor
University Hospital Schleswig-Holstein
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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