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Efficacy and Cost-effectiveness of Spasticity Treatment With Multifocal TENS

Primary Purpose

Spasticity, Stroke, Cerebral Palsy

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Multifocal TENS garment (Mollii®)
Sponsored by
Linkoeping University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spasticity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Spasticity due to stroke or Cerebral Palsy
  • Have some preserved walking ability, with or without walking aids
  • Be able to understand the treatment and instruments/interviews used
  • For stroke participants, two years should have elapsed since their injury/insult

Exclusion Criteria:

  • Electronic devices
  • Ventriculoperitoneal shunt
  • Arrhythmia
  • Hearth infarction or unstable angina pectoris
  • Symptomatic hyper- or hypotonia
  • Cancer under treatment
  • Unstable psychiatric disease
  • Lung disease, affecting daily life
  • Unstable epileptic disease
  • Orthopedic surgery last year
  • Obesity with BMI > 35
  • Infectious disease with longstanding treatment
  • Pregnancy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Sham Comparator

    Arm Label

    Multifocal TENS

    Sham treatment

    Arm Description

    Multifocal TENS given in the garment Mollii® (Elektrodress) 1 hour every second day together with individualized training exercises. The steering unit counts down 60 minutes visible for the patient

    Use of the garment Mollii® (Elektrodress) but without the electrical stimulation combined with the individualized training exercises. The steering unit counts down 60 minutes visible for the patient

    Outcomes

    Primary Outcome Measures

    Goal attainment scaling (GAS)
    1 to 3 goals are defined and evaluated using the original GAS scale by Kiresuk
    Arm-hand ability (ARAT + WMFT tasks 1&2)
    Action Research Arm Test (ARAT)measuring grasp, grip, pinch and gross movement and this is complemented by Wolf Motor Function Test (WMFT) tasks 1 and 2 measuring active shoulder abduction
    Mobility
    10 meter walking test, divided into comfortable gait test (CGT) and fast gait test (FGT). Outcome is velocity, cadence and stride length. Timed Up & Go (TUG)

    Secondary Outcome Measures

    Health related Quality of Life/QALY
    SF-36 and EQ-VAS
    Self reported pain and spasticity
    Numeric rating scale (NRS)
    Muscle hypertonicity (Spasticity)
    Modified Ashworth scale (0-5)
    Range of Motion
    Goniometer
    Costs
    Costs directly related to intervention Baseline, week 6, 12, 18 Costs from a societal perspective at baseline and week 52
    Goal Attainment Scaling (GAS)
    1 to 3 goals are defined and evaluated using the original GAS scale by Kiresuk
    Arm-hand ability (ARAT + WMFT tasks 1&2)
    Action Research Arm Test (ARAT)measuring grasp, grip, pinch and gross movement and this is complemented by Wolf Motor Function Test (WMFT) tasks 1 and 2 measuring active shoulder abduction
    Mobility
    10 meter walking test, divided into comfortable gait test (CGT) and fast gait test (FGT). Outcome is velocity, cadence and stride length. Timed Up & Go (TUG)

    Full Information

    First Posted
    October 1, 2014
    Last Updated
    July 10, 2015
    Sponsor
    Linkoeping University
    Collaborators
    University of Borås, University Hospital, Linkoeping, Sodra Alvsborgs Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02261142
    Brief Title
    Efficacy and Cost-effectiveness of Spasticity Treatment With Multifocal TENS
    Official Title
    Evaluation of Efficacy and Cost-effectiveness of Spasticity Treatment With Multifocal Transcutaneous Electrical Stimulation, Through a Garment With built-in Electrodes in Combination With Training.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2013 (undefined)
    Primary Completion Date
    February 2015 (Actual)
    Study Completion Date
    February 2015 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Linkoeping University
    Collaborators
    University of Borås, University Hospital, Linkoeping, Sodra Alvsborgs Hospital

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Spasticity is a common consequence of injury to the central nervous system and can be a major problem in motor function and everyday activities. A method for treating spasticity that applies low-amplitude electrical stimulation through a garment with built-in electrodes, Mollii® (Elektrodress), has been developed. The garment is to be used in combination with individualized training and the stimulation is mainly given to antagonists of spastic muscles. The general objective of this study is to evaluate the efficacy of and costs associated with the Mollii® treatment of spasticity due to stroke or cerebral palsy. Primary objectives are; to study whether treatment with the Mollii® improves function and activity to evaluate the cost-effectiveness of the treatment, from both a health-care perspective and a societal perspective. Secondary objectives are; to study whether there are differences in treatment effect between the stroke and the Cerebral Palsy groups in a subgroup-analysis to assess compliance with treatment to report any adverse effects.
    Detailed Description
    This study is designed as a double-blinded, randomized, cross-over trial (RCT). This part of the study takes 12 weeks (6 weeks of active treatment and 6 weeks of non-active treatment) and is followed by a wash-out period of 6 weeks. An uncontrolled,open phase starts after week 18, where patients are followed one year after inclusion. 30 participants with spasticity due to Stroke and Cerebral Palsy will be included. Two centers are recruiting participants and are collecting data. Outcome measures are chosen to reflect the different dimensions in the International Classification of Functioning, Disability and Health (ICF) and patient reported outcome measures (PROM).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Spasticity, Stroke, Cerebral Palsy

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    31 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Multifocal TENS
    Arm Type
    Experimental
    Arm Description
    Multifocal TENS given in the garment Mollii® (Elektrodress) 1 hour every second day together with individualized training exercises. The steering unit counts down 60 minutes visible for the patient
    Arm Title
    Sham treatment
    Arm Type
    Sham Comparator
    Arm Description
    Use of the garment Mollii® (Elektrodress) but without the electrical stimulation combined with the individualized training exercises. The steering unit counts down 60 minutes visible for the patient
    Intervention Type
    Device
    Intervention Name(s)
    Multifocal TENS garment (Mollii®)
    Other Intervention Name(s)
    Mollii®, Elektrodress, Swedish patent:SE534365.C2
    Intervention Description
    Multifocal transcutaneous electrical stimulation incorporated into a whole-body garment in combination with training
    Primary Outcome Measure Information:
    Title
    Goal attainment scaling (GAS)
    Description
    1 to 3 goals are defined and evaluated using the original GAS scale by Kiresuk
    Time Frame
    12 weeks
    Title
    Arm-hand ability (ARAT + WMFT tasks 1&2)
    Description
    Action Research Arm Test (ARAT)measuring grasp, grip, pinch and gross movement and this is complemented by Wolf Motor Function Test (WMFT) tasks 1 and 2 measuring active shoulder abduction
    Time Frame
    12 weeks
    Title
    Mobility
    Description
    10 meter walking test, divided into comfortable gait test (CGT) and fast gait test (FGT). Outcome is velocity, cadence and stride length. Timed Up & Go (TUG)
    Time Frame
    12 weeks
    Secondary Outcome Measure Information:
    Title
    Health related Quality of Life/QALY
    Description
    SF-36 and EQ-VAS
    Time Frame
    Baseline, week 6, 12, 18, 52
    Title
    Self reported pain and spasticity
    Description
    Numeric rating scale (NRS)
    Time Frame
    Baseline, week 6, 12, 18, 52
    Title
    Muscle hypertonicity (Spasticity)
    Description
    Modified Ashworth scale (0-5)
    Time Frame
    Baseline, week 6, 12, 18, 52
    Title
    Range of Motion
    Description
    Goniometer
    Time Frame
    Baseline, week 6, 12, 18, 52
    Title
    Costs
    Description
    Costs directly related to intervention Baseline, week 6, 12, 18 Costs from a societal perspective at baseline and week 52
    Time Frame
    Baseline, week 6, 12, 18, 52
    Title
    Goal Attainment Scaling (GAS)
    Description
    1 to 3 goals are defined and evaluated using the original GAS scale by Kiresuk
    Time Frame
    52 weeks
    Title
    Arm-hand ability (ARAT + WMFT tasks 1&2)
    Description
    Action Research Arm Test (ARAT)measuring grasp, grip, pinch and gross movement and this is complemented by Wolf Motor Function Test (WMFT) tasks 1 and 2 measuring active shoulder abduction
    Time Frame
    52 weeks
    Title
    Mobility
    Description
    10 meter walking test, divided into comfortable gait test (CGT) and fast gait test (FGT). Outcome is velocity, cadence and stride length. Timed Up & Go (TUG)
    Time Frame
    52 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Spasticity due to stroke or Cerebral Palsy Have some preserved walking ability, with or without walking aids Be able to understand the treatment and instruments/interviews used For stroke participants, two years should have elapsed since their injury/insult Exclusion Criteria: Electronic devices Ventriculoperitoneal shunt Arrhythmia Hearth infarction or unstable angina pectoris Symptomatic hyper- or hypotonia Cancer under treatment Unstable psychiatric disease Lung disease, affecting daily life Unstable epileptic disease Orthopedic surgery last year Obesity with BMI > 35 Infectious disease with longstanding treatment Pregnancy

    12. IPD Sharing Statement

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