Feasibility Study of Physiotherapy for Functional Motor Symptoms
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT02275000|
Recruitment Status : Completed
First Posted : October 27, 2014
Last Update Posted : May 16, 2016
|Condition or disease||Intervention/treatment||Phase|
|Conversion Disorder||Other: 5 Day Physiotherapy Programme Other: Physiotherapy||Not Applicable|
Participants will be recruited from outpatient neurology clinics at Queen Square. Those who consent to take part will complete baseline outcome measures (Time 1) before being randomised to either a Treatment as Usual control group or the Intervention group.
Treatment as Usual group -
- Participants will be directed to online patient information resources (www.neurosymptoms.org)
- Participants will be placed on the waiting list to be assessed for the inpatient treatment programme for functional symptoms at The National Hospital for Neurology and Neurosurgery. The waitlist is currently greater than 12 months.
- A referral is made to local community therapy services (which may include physiotherapy, occupational therapy and psychological therapy). If the participant has had contact from their community therapy services in the previous 12 months, a letter summarising the participant's diagnosis and physiotherapy needs will be sent.
- Participants will be asked to return at 4 weeks to complete outcome measures for a second time (Time 2)
A referral to community therapy for such patients is usual practice in the UK, although the form in which the community therapy is provided tends to be inconsistent across the UK. In most cases it will entail between 1 and 8 outpatient or domiciliary physiotherapy appointments. Some communities will have access to Occupational Therapy, which may entail supported practice and advice to increase independence with functional tasks and the provision of equipment. The provision of community therapy to participants will be monitored through the CSRI.
Intervention Group -
For participants allocated to the intervention group, a 5 day admission on the Day Hospital at the National Hospital for Neurology and Neurosurgery is arranged. The physiotherapy intervention will take place in the physiotherapy department. Participants will be admitted individually (and not in groups). Outside of physiotherapy times participants are encouraged to rest in the day hospital and complete a workbook. A single independent physiotherapist will be trained to deliver the intervention.
The participant (+/- family member) will attend an initial meeting with the consultant neurologist and the treating physiotherapist. The neurologist will perform a brief neurological assessment and confirm the diagnosis.
- The diagnosis will be explained again to the patient, using the word "functional" to describe the diagnosis.
- Physical signs of FMS will be demonstrated to the patient. This includes distractibility, Hoover's sign and entrainment.
- The treatment programme will be explained to the patient, linking resolution of symptoms with treatment rationale.
- The participant will attend 8-9 physiotherapy sessions over the 5 days. The intervention is a combination of education on functional motor symptoms, movement retraining and development of a self management plan.
- After the final physiotherapy session, the participant will complete the outcome measures (Time 2) and a feedback form.
Both groups will be followed up at 6 months after recruitment to the study (Time 3). An independent assessor will administer the outcome measures.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||60 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Randomised Feasibility Study of a Physiotherapy Programme for Patients With Functional Motor Symptoms (FMS).|
|Study Start Date :||September 2014|
|Actual Primary Completion Date :||January 2016|
|Actual Study Completion Date :||January 2016|
5 Day physiotherapy programme at the National Hospital for Neurology and Neurosurgery, Queen Square, London UK.
Other: 5 Day Physiotherapy Programme
The experimental group will complete a 5 day physiotherapy programme consisting of education, movement retraining and a self management plan.
Active Comparator: Treatment as usual
Participants are referred to their local neuro-physiotherapy service and if appropriate placed on a waiting list for inpatient rehabilitation.
Treatment as usual physiotherapy. The participant will be referred to their closest NHS outpatient neuro-physiotherapy service.
- Clinical Global Impression Scale of Change [ Time Frame: Approximately 4 weeks after randomisation (this will be immediately after treatment for the experimental arm) and 6 months ]Self rated 5 point Likert scale of change
- Short Form 36 [ Time Frame: Baseline and 6 months ]
- Hospital Anxiety and Depression Scale [ Time Frame: Baseline, approximately 4 weeks after randomisation and 6 months ]
- EQ-5D-5L [ Time Frame: Baseline, approximately 4 weeks after randomisation and 6 months ]
- Brief Illness Perception Questionnaire [ Time Frame: Baseline, approximately 4 weeks after randomisation and 6 months ]
- Work and Social Adjustment Scale [ Time Frame: Baseline, approximately 4 weeks after randomisation and 6 months ]
- Disabilities of the Arm, Shoulder and Hand (DASH) [ Time Frame: Baseline, approximately 4 weeks after randomisation and 6 months ]self reported questionnaire of upper limb function
- Functional Mobility Scale [ Time Frame: Baseline, approximately 4 weeks after randomisation and 6 months ]Scale of assistance required when walking 5, 50 and 500 metres.
- Psychogenic Movement Disorders Rating Scale (PMDRS) [ Time Frame: Baseline, approximately 4 weeks after randomisation and 6 months ]Blind video analysis of movement
- Berg Balance Scale [ Time Frame: Baseline, approximately 4 weeks after randomisation and 6 months ]
- 10 metre Walk Test [ Time Frame: Baseline, approximately 4 weeks after randomisation and 6 months ]timed walk over 10 metres
- Client Services Receipt Inventory (CSRI) [ Time Frame: Baseline and 6 month follow up ]This questionnaire collects retrospective information about the use of health and social care services, income, employment and benefits. It can be used to calculate service costs and total costs of care.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02275000
|The National Hospital for Neurology and Neurosurgery|
|London, United Kingdom, WC1N 3BG|
|Principal Investigator:||Glenn Nielsen||UCL|