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
About this trial
This is an interventional treatment trial for Spasticity
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
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
NCT ID
NCT02261142
First Posted
October 1, 2014
Last Updated
July 10, 2015
Sponsor
Linkoeping University
Collaborators
University of Borås, University Hospital, Linkoeping, Sodra Alvsborgs Hospital
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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Efficacy and Cost-effectiveness of Spasticity Treatment With Multifocal TENS
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