Functional Motor Disorders
Conditions
Keywords
Virtual Reality
Brief summary
The study aims to demonstrate the effectiveness and superiority of a 5-day immersive VR-rehabilitation treatment versus a 5-day conventional rehabilitation treatment in reducing FMDs symptoms severity, assessed by the Simplified Functional Movement Disorders Rating Scale (S- FMDRS).
Detailed description
This is a single-blind, randomized controlled trial to evaluate the superiority of immersive VR distractors combined with graded physical exercises over conventional rehabilitation (without any VR distractors) to reduce FMDs symptoms and improve gait and balance. Patients will be randomized to receive the experimental training (VRG) or the control training (CRG) (allocation ratio 1:1). The primary and secondary outcomes will be measured by the same examiner before (T0), at the end of the treatment (T1), and at three-month follow-up after the end of the treatment (T2). The test order will be the same across all evaluation sessions. The examiner will be blinded to group assignments.
Interventions
Virtual reality (VR) is a powerful tool to create an illusory state in which the user can feel that they have been transported to a new location (place illusion), that events happening are real (plausibility illusion), and even that bodies have been substituted by an avatar (embodiment illusion). VR illusions are driven by the same neurological mechanisms of everyday perception of the body in the world and induce realistic responses to VR.
BEHAVIORALControl Group intervention
Treatment will follow general treatment principles in physiotherapy for FMDs: (1) education; (2) exploration of how symptoms affect movement and posture; (3) retraining movement using strategies based on redirection of attention; and (4) development of a self-management plan.
Sponsors
Marialuisa Gandolfi
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
An examiner blinded to group allocation will assess all patients. To keep blindness, the examiner will not ask for information about the treatment to the patients or the caregivers, and this last will be instructed not to give any extra information outside of the examiner's questions.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
were: established diagnosis of FMDs, age ≥ 18 years, and acceptance of the diagnosis.
Exclusion criteria
were: prominent dissociative seizures, prominent cognitive and/or physical impairment that precluded signing the informed consent form for study participation based on clinical judgment, incomplete assessment, and questionnaire because of language comprehension difficulties.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in the Simplified Functional Movement Disorders Rating Scale (S-FMDRS) score | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | Objective-rated validated scale to rate the duration and severity of functional motor symptoms (range: 0-54; higher = worse). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in gait speed (cm/sec) | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | Gait analysis will be used to collect gait speed (cm/s). |
| Change in total excursion path (mm) | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | An electronic monaxial stabilometric platform will be used to collect total excursion path (mm). |
| Change in velocity of Cop displacement in the anteroposterior directions (mm/s) | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | An electronic monaxial stabilometric platform will be used to collect the velocity of Cop displacement in the anteroposterior directions. |
| Change in velocity of Cop displacement in the mediolateral directions (mm/s) | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | An electronic monaxial stabilometric platform will be used to collect the velocity of Cop displacement in the mediolateral directions. |
| Change in the Toronto Alexithymia Scale (TAS-20) score | Before the intensive 5-day rehabilitation program (T0) and after 12 weeks (T2). | It evaluates the level of alexithymia (range: 20-100; higher = worse) |
| Change in the Multidimensional Fatigue Inventory Scale (MFI-20) score | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | It evaluates fatigue differentiating general, physical, reduced-activity, reduced-motivation, and mental fatigue (subscale range: 4-20; higher = worse). |
| Change in the Brief Pain Inventory (BPI) score | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | It evaluates pain intensity (range: 0-40; higher = worse) and interference (range: 0-70; higher = worse). |
| Change in the Beck Depression Inventory (BDI-II) score | Before the intensive 5-day rehabilitation program (T0) and after 12 weeks (T2). | It evaluates depression (range: 0-63; higher = worse). |
| Change in the Beck Anxiety Inventory (BAI) score | Before the intensive 5-day rehabilitation program (T0) and after 12 weeks (T2). | It evaluates anxiety (range: 0-63; higher = worse). |
| Change in the 12-item Short-Form Health Survey (SF-12) score | Before the intensive 5-day rehabilitation program (T0) and after 12 weeks (T2). | The health-Related QoL will be evaluated by the Mental Health and Physical functioning of the 12-item Short-Form Health Survey (SF-12) (range: 0-100; higher = better) |
| Change in the Clinical Global Impression (CGI) score | Before the intensive 5-day rehabilitation program (T0) and after 12 weeks (T2). | Self-rated perception of change will be assessed with the 7-point Clinical Global Impression (CGI) scale with scores from 1 (very much improved) to 7 (very much worse). |
| Change in Swing time (%) | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | Gait analysis will be used to collect swing time (%). |
| Change in Stride time (s) | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | Gait analysis will be used to collect stride time (s). |
| Change in Stride length (cm) | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | Gait analysis will be used to collect stride length (cm). |
| Change in sway area (mm2) | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1), and after 12 weeks (T2). | An electronic monaxial stabilometric platform will be used to collect sway area (mm2). |
Other
| Measure | Time frame | Description |
|---|---|---|
| number of falls or event near falling | after the intensive 5-day rehabilitation program (T1) | Falls or event near falling occurred during the rehabilitation in both groups |
| Score on the Simulation Sickness Questionnaire (SSQ) | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1) | It will be used to evaluate the level of symptoms associated with simulator sickness (subscale range: 0-48; higher=worse) |
| Number of drop-out | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1) | The number of dropouts before the end of treatment will be collected. The experimental group will report adverse events on the use of VR. |
| number of patients who refuse the treatment | Before the intensive 5-day rehabilitation program (T0), after the intensive 5-day rehabilitation program (T1) | Recruitment rate |
Countries
Italy
Contacts
Primary ContactMarialuisa Gandolfi, PhD
Backup ContactMichele Tinazzi, PhD
Outcome results
None listed