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Taking peoplePhase 2

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

Key facts

Who runs it
University Hospital Schleswig-Holstein
Where
Germany1 site in 1 countryChoose a country to see its sites
Trial code
Status
Recruiting
Phase
Phase 2
People taking part
54 people, planned
Started
26 Jun 2020
Expected to end
1 Jan 2027
Type of study
Interventional, 2 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • motor training
  • mindfulness exercises
Record updated
10 December 2024

Who can take part

Age
18 years to 80 years
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 9 criteriaShow less

Who can take part

  • 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

Who cannot take part

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

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

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.

The 2 groups in the trial

  • motor trainingTreatment being tested

    intervention: motor training

  • awareness trainingExisting treatment, for comparison

    intervention: mindfulness exercises

    Treatment: mindfulness exercises

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Treatment Effect and Relevance on Daily Life of a Video-supervised Sensorimotor Training Program and Its Influence on the Pathophysiology in Writer's Cramp
Fit questions
Built from NCT04611009, who can take part
Record updated
10 December 2024