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Conversion DisorderNCT05943652

Observational Study on "Functional Overlay" in Patients With Movement Disorders

An observational study of Conversion Disorder and Parkinson Disease, run by Medical University of Graz at 1 site in Austria.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The goal of this observational study is to learn about functional neurological disorders in patients with common non-functional movement disorders ("functional overlay"). The main questions it aims to answer are: What is the frequency of functional neurological disorders in patients with non-functional movement… Read more about this study

Who is it for?
Ages 18 to 18 years
Conditions the study is for
Conversion Disorder, Parkinson Disease, Tremor
What is being tested?
Neurological examination, Anamnesis and Neuropsychological testing
Type of treatment
Injection or infusion
How many people
216 participants
Where
1 siteAustria
Study dates
1 Jan 2023to 30 Jun 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 18 years
  • All sexes
  • Adult

Study population: Patients with functional and non-functional movement disorders of the Movement Disorders Outpatient Clinic of the Department of Neurology, Medical University of Graz

Who may be able to join

  • Functional or non-functional movement disorder
  • 18 to 80 years

Who cannot join

  • Patient is not able to consent
  • Patient is not able to understand / speak German fluently (questionnaires are available only in German)

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Austria1 site, 1 recruiting
  • Medical University of graz

    Graz, Styria, 8010

    Daniela Kern, MD, 004331638516051, daniela.eibl@medunigraz.at

    Recruiting

Other trials in Austria

About this study

Official title: Prevalence and Clinical Presentation of Functional Neurological Disorders in Patients With Movement Disorders - A Cross-sectional Study in the Movement Disorders Clinic of the Department of Neurology, Medical University of Graz

The goal of this observational study is to learn about functional neurological disorders in patients with common non-functional movement disorders ("functional overlay"). The main questions it aims to answer are:

  • What is the frequency of functional neurological disorders in patients with non-functional movement disorders (functional overlay)?
  • What are the characteristics of functional neurological disorders in patients with non-functional movement disorders?
Read more

Participants will be examined clinically and electrophysiologically, the examinations consist of:

  • a neurological examination
  • neuropsychological testing
  • electrophysiological tremor diagnostic
  • questionnaires about psychological, biological and social risk factors

Researchers will compare patients with functional motor disorders to patients wit non-functional movement disorders to see if they differ from each other regarding the functional symptoms.

Read the detailed description

Functional neurological disorders (FND) are common neurological disorders that are present in up to 16% of patients in neurological outpatient clinics. They are associated with a significant reduction in quality of life, can lead to permanent impairment, and have a poor prognosis, especially if the diagnosis is delayed.

FND have multifactorial causes and risk factors, including psychological stressors, childhood trauma, female gender, psychiatric disorders such as depression, anxiety disorder, or post-traumatic stress disorder, and other functional disorders such as irritable bowel syndrome or chronic pain syndrome. Patients with FND often report additional cognitive complaints ("cognitive fog").

A mismatch of various regulatory mechanisms, a disruption of sensory processing and motor output is assumed to be a central part of the pathogenesis. A characteristic feature of FND is a variability of symptoms according to attention. FND can be intensified by increased attention and weakened by distraction. Positive diagnostic criteria for FND have been established recently, so that by definition FND are no longer a diagnosis of exclusion.

The clinical presentations of FND are diverse and include impaired limb movement control, disturbances in vigilance that may be associated with seizures, and non-motor symptoms. FND often coincide and often coexist with pain, fatigue, sleep disorders, and cognitive disorders. Particularly non-motor functional symptoms are highly debilitating for patients.

The coincidence of "organic" neurological disorders and FND in the same patients ("functional overlay") is probably not uncommon, but has been investigated primarily in patients with Parkinson's Disease and epilepsy, so far. However, it is important to recognize FND in patients with movement disorders in order to treat them adequately and to protect them from incorrect treatment (surgery, unnecessary medication, etc.). However, the basic prerequisite for this is an exploration of the frequency and characteristics of the functional symptoms in movement disorders.

Being tested
Neurological examination, Anamnesis, Neuropsychological testing, Questionnaires, Tremor recording
Keywords
Accelerometry, Patient Health Questionnaire, Neuropsychology
Medical subject headings
Conversion Disorder, Parkinson Disease, Tremor, Dystonia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Neurological examinationDiagnostic test

    A neurological examination following a protocol to detect positive signs of functional neurological disorders.

  • AnamnesisDiagnostic test

    A standardized question about the patient´s history. The response time is measured.

    Question: "Could you tell me about the problems with the movement disorder you are experiencing?"

  • Neuropsychological testingDiagnostic test

    Neuropsychological cognitive testing including:

    • Montreal Cognitive Assessment (MOCA)
    • Rey-Osterrieth Complex Figure Test (ROCFT)
    • Wechsler Memory Scale IV
    • Comprehensive Trail Making Test (CTMT)
    • semantic and phonematic fluency tests
  • QuestionnairesDiagnostic test

    • Short Form 36 (SF 36)
    • Somatic Symptom Disorder - B Criteria Scale (SSD 12)
    • Patient Health Questionnaire 9 (PHQ 9)
    • Patient Health Questionnaire 15 (PHQ 15)
    • Generalized Anxiety Disorder 7 (GAD 7)
    • Fatigue Severity Scale (FSS)
    • Psychosomatic Competence Inventory (PSCI)
    • Work Ability Index (WAI)
    • Level of Personality Functioning Scale
    • Toronto Alexithymia Scale
    • Levels of Emotional Awareness Scale (short version)
    • Certainty About Mental States Questionnaire
    • Somatosensoric Amplification Scale
    • Personality Inventory for DSM-5 short version (PID5BF+M)
    • Childhood Trauma Questionnaire
    • European Quality of Life 5 Dimensions 5 Level Version (EQ5D5L)
  • Tremor recordingDiagnostic test

    Accelerometry following a standardized protocol, using a triaxial accelerometer transducer (Biometrics ACL300, Sensitivity 6 100 mV/G, Biometrics Ltd, UK)

Study groups in NCT05943652
Study groupRoleWhat they receive
Parkinson DiseaseNot described
Receives: Diagnostic Test: Neurological examination; Diagnostic Test: Anamnesis; Diagnostic Test: Neuropsychological testing; Diagnostic Test: Questionnaires; Diagnostic Test: Tremor recording
Idiopathic DystoniaNot described
Receives: Diagnostic Test: Neurological examination; Diagnostic Test: Anamnesis; Diagnostic Test: Neuropsychological testing; Diagnostic Test: Questionnaires; Diagnostic Test: Tremor recording
Essential TremorNot described
Receives: Diagnostic Test: Neurological examination; Diagnostic Test: Anamnesis; Diagnostic Test: Neuropsychological testing; Diagnostic Test: Questionnaires; Diagnostic Test: Tremor recording
Functional Neurological DisorderNot described
Receives: Diagnostic Test: Neurological examination; Diagnostic Test: Anamnesis; Diagnostic Test: Neuropsychological testing; Diagnostic Test: Questionnaires; Diagnostic Test: Tremor recording
Functional Cognitive DisorderNot described
Receives: Diagnostic Test: Neurological examination; Diagnostic Test: Anamnesis; Diagnostic Test: Neuropsychological testing; Diagnostic Test: Questionnaires; Diagnostic Test: Tremor recording
Alzheimer DiseaseNot described
Receives: Diagnostic Test: Neurological examination; Diagnostic Test: Anamnesis; Diagnostic Test: Neuropsychological testing; Diagnostic Test: Questionnaires; Diagnostic Test: Tremor recording

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Functional neurological symptoms

    Diagnosed by positive signs for functional neurological symptoms, as assessed in the neurological examination

    Measured: on average 30 minutes

Secondary outcomes (21)
  1. Duration of anamnesis

    Duration in seconds of the response to the question: "Could you tell me about the problems with the movement disorder you are experiencing?"

    Measured: 1 to 3 minutes

  2. Tremor diagnostic

    Sum score of a electrophysiological test battery for psychogenic tremor, a scale from 0 to 10 with higher numbers indicating a higher probability for functional tremor

    Measured: up to 20 minutes

  3. Subjective quality of life

    European Quality of Life 5 Dimensions 5 Level Version (EQ 5D 5L), results in a 5-digit number that describes the patient's health state

    Measured: 5 minutes

  4. Subjective health

    Short Form 36 Questionnaire (SF-36), a 36 items questionnaires that results in 8 scales that describe the subjective health state of the patient, higher values indicating better health

    Measured: up to 10 minutes

  5. Fatigue

    Fatigue severity scale (FSS): 9 item questionnaire with a 7 point Likert scale, higher values indicating more fatigue

    Measured: up to 5 minutes

  6. General anxiety

    General anxiety disorder scale 7 (GAD-7): a 7 items questionnaire (0 to 21 points, higher values indicating more anxiety)

    Measured: 3 minutes

  7. Somatic symptoms

    Patient health questionnaire 15 (PHQ 15): a 15 item questionnaire (0 to 30 points, higher values indicating more somatic symptoms)

    Measured: 5 minutes

  8. Depression

    Patient health questionnaire 9 (PHQ 9): a 9 item questionnaire (0 to 27 points, higher values indicating more depressive symptoms)

    Measured: 3 minutes

  9. Psychosomatic Competence

    Psychosomatic Competence Inventory (PSCI): a 44 items questionnaire with a 6 point Likert scale, resulting in 6 subscales, higher values indicate higher psychosomatic competence

    Measured: up to 10 minutes

  10. Work ability

    Work ability index (WAI): 7 item questionnaire, 7 to 49 points, with higher values indicating better work ability

    Measured: 5 minutes

  11. Trauma in childhood

    Child Trauma Questionnaire (CTQ): 28 items questionnaire, 5 point Likert scale, resulting in 5 subscales with 5 to 25 points, with higher values indicating more trauma experience

    Measured: up to 10 minutes

  12. Attachment styles

    Experience of Close Relationships-Revised (ECR-RD 12): 12 items questionnaire with a 7 point Likert scale, resulting in 2 subscales

    Measured: 5 minutes

  13. Alexithymia

    Toronto alexithymia scale (TAS): 26 items questionnaire with a 5 point Likert scale, higher values indicating more alexithymia

    Measured: 5 minutes

  14. Personality traits

    The Personality Inventory for DSM-5 and ICD-11 Plus Modified (PID5BF + M): a 36 items questionnaire, with a 4 point Likert scale, resulting in 6 subscales

    Measured: up to 10 minutes

  15. Personality functioning

    Levels of personality functioning scale (LPFS): a 80 items questionnaire, with a 4 point Likert scale, resulting in 4 subscales

    Measured: up to 15 minutes

  16. Executive function

    Comprehensive trail making test (CTMT)

    Measured: up to 10 minutes

  17. Memory

    Wechsler Memory Scale

    Measured: up to 15 minutes

  18. Visuospatial abilities

    Rey-Osterrieth complex figure test

    Measured: up to 15 minutes

  19. Functional cognitive symptoms

    Incongruence in cognitive tests

    Measured: up to 60 minutes

  20. Semantic word fluency

    number of animals that can be listed in 2 minutes

    Measured: 2 minutes

  21. phonematic word fluency

    number of words, that start with the letter "b", that can be listed in 2 minutes

    Measured: 2 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Jul 2023
  2. Study start1 Jan 2023
  3. Primary completion31 Dec 2025 (estimated)
  4. Study completion30 Jun 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
216 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05943652
Sponsor's protocol ID
34-509 ex 21/22
Status last verified
Sep 2025
First submitted
5 Jul 2023
Last updated
29 Sep 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Conversion Disorder and Parkinson Disease, run by Medical University of Graz at 1 site in Austria.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 29 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Austria. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Daniela Kern, MD (004331638516051, daniela.eibl@medunigraz.at), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Functional neurological symptoms (time frame: on average 30 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Sep 2025; AzTrials last refreshed its copy on 31 Oct 2026.

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