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TMS and Attentional Bias in Functional Motor Disorder

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ClinicalTrials.gov Identifier: NCT02102906
Recruitment Status : Completed
First Posted : April 3, 2014
Last Update Posted : February 9, 2016
Sponsor:
Information provided by (Responsible Party):
University of Edinburgh

Tracking Information
First Submitted Date  ICMJE March 31, 2014
First Posted Date  ICMJE April 3, 2014
Last Update Posted Date February 9, 2016
Study Start Date  ICMJE October 2014
Actual Primary Completion Date November 2015   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: April 4, 2014)
  • Patient-rated disability [ Time Frame: An average of 3 months after day of attendance for TMS treatment. ]
    SF36 score and Modified Rankin Score
  • Patient rated symptom severity [ Time Frame: An average of 3 months after day of attendance for TMS treatment ]
    Assessed using a Likert scale.
Original Primary Outcome Measures  ICMJE
 (submitted: March 31, 2014)
  • Patient-rated disability [ Time Frame: 3 months after treatment ]
    SF36 score and Modified Rankin Score
  • Patient rated symptom severity [ Time Frame: 3 months after treatment ]
    Assessed using a Likert scale.
Change History
Current Secondary Outcome Measures  ICMJE
 (submitted: April 4, 2014)
  • Grip strength [ Time Frame: Between 10 minutes and one hour before TMS treatment, and between 10 minutes and 1 hour after TMS treatment. ]
  • Hand tapping frequency [ Time Frame: Between 10 minutes and one hour before TMS treatment, and between 10 minutes and 1 hour after TMS treatment ]
  • Patient rated treatment discomfort [ Time Frame: Between 10 minutes and 1 hour after TMS treatment. ]
Original Secondary Outcome Measures  ICMJE
 (submitted: March 31, 2014)
  • Grip strength [ Time Frame: Immediately before and after treatment ]
  • Hand tapping frequency [ Time Frame: Immediately before and after treatment. ]
  • Patient rated treatment discomfort [ Time Frame: Immediately after treatment ]
Current Other Pre-specified Outcome Measures
 (submitted: April 4, 2014)
Attentional focus / distractibility [ Time Frame: Tests performed during the 1-2 hours before treatment. ]
A short series of neurocognitive experiments based on a modified Posner test will examine for differences in attentional focus between affected and unaffected limbs and will also compare performance with a group of healthy controls recruited from spouses.
Original Other Pre-specified Outcome Measures
 (submitted: March 31, 2014)
Attentional focus / distractibility [ Time Frame: Tests performed before treatment. ]
A short series of neurocognitive experiments based on a modified Posner test will examine for differences in attentional focus between affected and unaffected limbs and will also compare performance with a group of healthy controls recruited from spouses.
 
Descriptive Information
Brief Title  ICMJE TMS and Attentional Bias in Functional Motor Disorder
Official Title  ICMJE TMS and Attentional Bias in Functional Motor Disorder
Brief Summary

Functional motor disorders, also called motor conversion disorder, are common reasons for attendance at neurology outpatient clinics. Patients with functional motor disorders are more common than patients with multiple sclerosis and have similar levels of disability but more psychological morbidity.

There is limited evidence for effective treatments in functional motor disorders. A small number of studies of transcranial magnetic stimulation (TMS), a painless method of cortical stimulation, have reported improvement in functional weakness after this treatment including in patients with symptoms of several years duration. The Investigators intend to trial TMS in a group of 40 patients with functional motor disorder, randomising patients to immediate or delayed treatment and therefore comparing a single session of TMS with routine clinical care. The Investigators will also ask patients to undergo tests of attentional focus in a cognitive neuroscience laboratory - these experiments will be analysed separately from TMS trial data.

Detailed Description

A randomised non-blinded controlled study design will be used, with 3 months of treatment as usual as the control condition and a single session of TMS as the treatment condition.

40 patients with functional unilateral upper limb weakness will be recruited from neurology and neuropsychiatry clinics in Edinburgh and randomised to either immediate treatment or to 3 month delay during which they will receive routine clinical care. Randomisation will be performed using computerised random number generator by a person not involved with the study.

Patients randomised to delay will complete baseline measures of disability and motor function including SF36, modified Rankin score and study specific questionnaires, and will repeat these after 3 months. Patients undergoing immediate treatment will complete the same questionnaires immediately before and 3 months after treatment. All individuals receiving TMS treatment will undergo tests of grip strength and tapping frequency immediately before and after treatment.

The treatment and experiments involved will be as follows. Patients will attend the PPLS Cognitive Neuroscience Laboratory at George Square, University of Edinburgh for a single 2 hour session. During the first hour they will complete baseline symptom severity and disability questionnaires and will undertake a series of 3 experiments. Experiments involve participants sitting with their head on a chin-rest looking at either a computer screen or at lights projected onto their own hands, and for one experiment with a vibrating 'buzzer' taped to each hand. They will be asked to respond verbally in experiments which test their response to distracting attentional 'cues' either visual or vibrotactile. These experiments will take less than 1 hour. In anaylsis, performance will be compared between affected and unaffected sides (ie left hand and right hand), and will also be compared with performance of a group of 15 healthy control participants recruited from spouses or partners.

Patient participants will then receive treatment with 20 single pulses of TMS to the motor cortex at 120% motor threshold. These will cause visible and palpable 'jerks' of the affected limb. Between stimulations the researcher will offer verbal encouragement and ask the participant to move the affected limb if possible. Treatment will take less than 1 hour.

The primary outcome measures are patient-rated symptom severity and disability and simple statistical analysis will be used to compare outcome after 3 months of treatment as normal and 3 months after a single session of TMS treatment. Secondary outcome measures include grip strength and tapping frequency before and after treatment. Data will be analysed on an intention-to-treat basis. Data from attentional tests will be analysed separately.

Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE Conversion Disorder
Intervention  ICMJE Procedure: Transcranial magnetic stimulation
Single pulse TMS - 20 pulses at 120% motor threshold. Using the Magstim rapid 2 stimulator, which has a CE mark and will be used within the indications specified by the CE mark.
Study Arms  ICMJE Experimental: TMS treatment
Patients will receive a single session of 20 single pulses of TMS to motor cortex contralateral to affected upper limb at 120% motor threshold, with verbal encouragement throughout. Half of the patients recruited will be randomised to a 3 month delay during which they will receive treatment as normal.
Intervention: Procedure: Transcranial magnetic stimulation
Publications * McWhirter L, Ludwig L, Carson A, McIntosh RD, Stone J. Transcranial magnetic stimulation as a treatment for functional (psychogenic) upper limb weakness. J Psychosom Res. 2016 Oct;89:102-6. doi: 10.1016/j.jpsychores.2016.08.010. Epub 2016 Aug 25.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: February 8, 2016)
13
Original Estimated Enrollment  ICMJE
 (submitted: March 31, 2014)
40
Actual Study Completion Date  ICMJE November 2015
Actual Primary Completion Date November 2015   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • clinical diagnosis, by a consultant neurologist, of functional motor disorder
  • functional unilateral upper limb weakness present for 50% or more of the time
  • age 18-75
  • ability to give informed consent

Exclusion Criteria:

  • difficulties in understanding spoken or written English
  • history of epileptic seizures (non-epileptic seizures will not be an exclusion criteria)
  • alcohol dependence
  • severe co-morbid physical or psychiatric disorder
  • factitious disorder
  • patients unable to receive TMS because of metal implants such as pacemakers
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 18 Years to 75 Years   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE United Kingdom
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT02102906
Other Study ID Numbers  ICMJE TMS
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement  ICMJE Not Provided
Responsible Party University of Edinburgh
Study Sponsor  ICMJE University of Edinburgh
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Principal Investigator: Jon Stone, MBChB PhD FRCP NHS Lothian
PRS Account University of Edinburgh
Verification Date December 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP