Writer's Cramp

2

Review clinical trials related to Writer's Cramp. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Brain Networks in Dystonia

To date, there is only limited knowledge about the distinct neural abnormalities that lead to the development of different forms of focal dystonia. The goal of this study is to dissect the pathophysiological mechanisms underlying this clinical phenomenon using multi-level brain network analysis in patients with focal dystonia.

Participants needed: 141
Trial details
Age: 21-80Biological sex: AllType: ObservationalSponsor: Massachusetts Eye and Ear InfirmaryUpdated: Dec 8, 2025Locations: 1
Eligibility criteria

Patients will have clinically documented focal dystonia [+5]

Subjects who are incapable of giving an informed consent. [+8]

Status: Recruiting

Video-supervised Motor and Awareness Training in Writer's Cramp

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.

Participants needed: 54
Trial details
Phase: Phase 2Age: 18-80Biological sex: AllType: InterventionalSponsor: University Hospital Schleswig-HolsteinUpdated: Dec 10, 2024Locations: 1
Eligibility criteria

Right handed idiopathic WC according to standardized criteria (simple and comple... [+1]

Additional neurological or psychiatric diseases [+6]