Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
48 participants
INTERVENTIONAL
2024-05-01
2026-03-30
Brief Summary
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Detailed Description
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There are three groups: Patients with functional tremor (FT), patients with essential tremor (ET) and healthy controls (HC). The study is carried out on one or two consecutive days. The first appointment is only made for patients with ET and FT and is used for the neurological examination and to assess the severity of the tremor. It takes place at the Outpatient Clinic for Movement Disorders at the University Clinic for Neurology in Graz and lasts a maximum of 30 minutes. The second appointment is at the Institute of Psychology at the University of Graz and requires the active participation of the respondent for 2.5 hours. Subjects are asked not to take any tremor-influencing medication on the day of the examination. HC will only attend the appointment at the Institute of Psychology.
First appointment:
* Clinical Global Impression - Severity Scale (CGI-S): 5-point Likert scale, clinicians assess the severity of the condition
* Patient Global Impression of Severity (PGI-S): 5-point Likert scale, patients assess the severity of the condition
* Fahn Tolosa Marin Tremor Rating Scale (FTM): assesses the tremor severity
* Simplified Version of the Functional Movement Disorders Rating Scale (S-FMDRS): assesses the severity of the functional tremor
Second appointment:
1. Questionnaires:
* Simulator Sickness Questionnaire (SSQ): 4-point Likert scale, assesses nausea, oculomotor and visual disturbances, disorientation (2 timepoints: before and after VR tasks)
* Edinburgh Handedness Inventory (EDI)
* Questionnaire about sociodemographic data
* Technology Usage Inventory (TUI): 7-point Likert scale, acceptance and use of technologies
* Igroup Presence Questionnaire (IPQ): sense of presence in the VR
2. electroencephalogram (EEG) and surface-Electromyography (surface-EMG) of forearm muscles: run synchronously with the examinations
3. VR-tasks: all tasks are carried out in randomized order
1. 3x3 matrix: individual fields light up in random order, participants are instructed to touch the fields in the given sequence as quickly as possible. 30 repetitions with a realistic VR-hand model and 30 repetitions with an abstract VR-hand model.
2. 3x3 matrix: same task as (a) but after each repetition, participants must touch a field labeled "next" to continue the task. 30 repetitions.
3. apple in a box: a virtual apple is to be placed in a virtual box using the hand with the weaker tremor, while the other hand is left resting on the table. 30 repetitions.
4. apple in a box: same task as (c) but the resting hand is not visible. 30 repetitions.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
BASIC_SCIENCE
SINGLE
Study Groups
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Functional Movement Disorder
Virtual reality motor task
After a short practice task, participants perform motor tasks in a virtual reality environment. Reaction time is used to assess task performance.
Essential Tremor
Virtual reality motor task
After a short practice task, participants perform motor tasks in a virtual reality environment. Reaction time is used to assess task performance.
Healthy Control
Virtual reality motor task
After a short practice task, participants perform motor tasks in a virtual reality environment. Reaction time is used to assess task performance.
Interventions
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Virtual reality motor task
After a short practice task, participants perform motor tasks in a virtual reality environment. Reaction time is used to assess task performance.
Eligibility Criteria
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Inclusion Criteria
* In patients with FT and ET: presence of a constant or intermittent tremor during the neurological examination
Exclusion Criteria
* essential tremor plus (ET plus)
* conditions that interfere with EEG diagnostic (skin conditions, skin infections, wounds)
* reflex epilepsy
* cervical degeneration or chronic pain syndrome of the cervical spine
* severe somatic illness
* previous cerebral or head surgery
* implanted pacemaker or deep brain stimulation
* persons who are unable to consent
18 Years
65 Years
ALL
Yes
Sponsors
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Medical University of Graz
OTHER
Responsible Party
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Principal Investigators
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Petra Schwingenschuh, MD
Role: PRINCIPAL_INVESTIGATOR
Medical University of Graz
Locations
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Medical University of Graz, Department of Neurology
Graz, , Austria
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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36-115 ex 23/24
Identifier Type: -
Identifier Source: org_study_id
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