Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
ID07588282

Psychoeducational Diagnosis Communication Impact on Illness Perception, Satisfaction, and Behavior in Functional Neurological Movement Disorders Using a Within-Subject Intervention Design

Led by Medical University of Graz · Updated on 2026-05-14

35

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Functional neurological movement disorders are common conditions that can cause significant limitations in daily life and result from a functional brain disorder. Researchers are studying how a clear, detailed, and empathetic explanation of the diagnosis affects patients' understanding of their condition, symptom progression, and their experience of communication with their doctor. The study also includes a one-time brain imaging scan to explore possible differences in brain function related to symptom changes and quality of life. Participants will receive a structured psychoeducational communication session delivered by physicians using a 14-step framework designed to explain the diagnosis of functional movement disorders. This approach aims to foster a shared understanding of the condition, validate patient experiences, and support rehabilitation efforts. The study follows a within-subject design, with assessments at baseline, before diagnosis, immediately after diagnosis, four weeks later, and three months later. During the study, participants will complete questionnaires and undergo assessments related to illness perception, symptom burden, trust in diagnosis, communication quality, and intentions about seeking additional medical opinions. Physicians' confidence in communicating the diagnosis will also be evaluated. A one-time MRI scan will be performed to examine brain anatomy and function. The total participation period includes a four-week waiting phase without intervention, followed by multiple follow-up assessments to monitor changes over time.

CONDITIONS

Brief Title

The Effect of Psychoeducational Diagnosis Communication on Perception of Illness, Satisfaction, and Behavioral Intentions Among Patients With Functional Neurological Movement Disorders

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 80 years
  • Diagnosis of one or more functional movement disorders such as functional paralysis, seizures, tremor, drop attacks, dystonia, twitching, facial symptoms, tics, or parkinsonism
  • Ability to give informed consent
  • Sufficient German language skills to complete questionnaires
Not Eligible

You will not qualify if you...

  • Unable to give informed consent
  • Temporarily unable to give informed consent
  • Insufficient German language skills to answer the questionnaires

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Baseline Assessment and Waiting Period

Duration - 4 weeks

Participants complete initial assessments and then undergo a four-week waiting period without intervention to serve as a control condition.

1 baseline visit and 1 visit before intervention

Outpatient Treatment

Duration - 1 day (single session)

Participants receive a structured psychoeducational communication session where physicians provide an empathetic and evidence-based explanation of the diagnosis of Functional Movement Disorders.

1 intervention visit (in-person)

Follow-up

Duration - 3 months

Participants complete repeated measurements to assess illness perception, trust in diagnosis, symptom burden, and other outcomes at multiple time points up to 3 months after the intervention.

Visits at immediately post-intervention, 4 weeks later, and 3 months later

Trial Site Locations

Total: 1 location

1

Medical University of Graz

Graz, Austria, 8036

Actively Recruiting

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Research Team

M

Maria Schneller

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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