Can Transcutaneous Electrical Stimulation Garment Improve Gait in Children With Cerebral Palsy?

Cerebral Palsy Clinical Trial

Official title:

Effectiveness in Improving Gait and Feasibility of a Transcutaneous Electrical Stimulation Garment in Children With Cerebral Palsy in Singapore

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04715334
• Other study ID #: 2020/2150
• Status: Recruiting
• Phase: N/A
• Start date: December 8, 2020
• Est. completion date: December 31, 2021

Study information

• Verified date: January 2021
• Source: KK Women's and Children's Hospital
• Contact: Zhi Min Ng, MBBS
• Phone: +65-6394 8975
• Email: ng.zhi.min[@]singhealth.com.sg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Living with cerebral palsy is challenging for the child as well as the family charged with their care and support needs. Many families seek effective and sustainable interventions to improve gait of their children with cerebral palsy. The Mollii suit is a non-invasive therapeutic technology using electrical stimulation in the form of whole-body garment with multiple electrodes individually programmed to stimulate selected muscles. This study aims to examine if the Mollii suit improve gait in ambulant children with cerebral palsy and if the Mollii suit is acceptable and tolerable to children with cerebral palsy. We will recruit up to 20 children with cerebral palsy. This study will evaluate change in gait and function following a four-week intervention period using a protocol of wearing the Mollii suit at home for one hour every day for four weeks using instrumented 3-dimensional gait analysis and objective standardised assessment tools.

Description:

BACKGROUND Living with cerebral palsy is challenging for the child as well as the family charged with their care and support needs. Many families seek effective and sustainable interventions to improve gait of their children with cerebral palsy. An intervention that could be used in the home setting, assessed periodically by health care professionals of a tertiary pediatric centre, that has a benefit on gait and motor function in children with cerebral palsy might be feasible to families in the local Singapore healthcare setting. The Mollii suit is a non-invasive therapeutic technology using electrical stimulation in the form of whole-body garment with multiple electrodes individually programmed to stimulate selected muscles. Based on small preliminary studies, it is suggested that the Mollii suit improves mobility, gait, function and quality of life. OBJECTIVES This study aims to examine the effectiveness of the Mollii suit in improving gait in children with cerebral palsy. It also aims to determine the value of the Mollii suit by evaluating the acceptability, tolerance and compliance of the Mollii suit in children with cerebral palsy. METHODOLOGY This is a single-centre study that will recruit up to 20 children with cerebral palsy, GMFCS I-III. This study will evaluate change in gait and function following a four-week intervention period using a protocol of wearing the Mollii suit at home for one hour every day for four weeks using instrumented 3-dimensional gait analysis and objective standardised assessment tools. Primary outcome is improvement in gait, measured using the Gait Profile Score, Gait Deviation index, gait speed and cadence. Secondary outcomes include changes in functional assessments such as Functional Assessment Questionnaire (FAQ), Gross Motor Function Measure (GMFM), 10 metre walk test, Goal attainment Scale (GAS) and quality of life measures.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. completion date: December 31, 2021
• Est. primary completion date: December 31, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 4 Years to 18 Years

Eligibility

Inclusion Criteria:

• Aged 4-18
• GMFCS level I to III
• Spasticity as the dominant motor feature
• Children agree to wear the Mollii suit as per procedures and consent to the study
• Parents/carers agree to assist their child to wear the Mollii suit as per procedures
• Medical practitioner's approval

Exclusion Criteria:

• Individuals with electrical implanted stimulatory device
• Individuals with medical devices that are affected by magnets, such as programmable shunts.
• Individuals with cardiovascular diseases, infectious diseases, malignance (cancer), fever, pregnancy, rashes or skin problems.
• Individuals who have had Botulinum toxin done 6 months prior intervention or soft tissue release surgery done 6 months prior intervention.
• Individuals who have had change in oral medication for spasticity 1 month prior intervention.

Related Conditions & MeSH terms

• Cerebral Palsy
• Muscle Spasticity
• Spasticity, Muscle

Intervention

Device:
• Mollii suit
The Mollii suit is a new technology of electrical stimulation in the form of whole-body garment with multiple electrodes individually programmed to stimulate the selected muscles. Based on preliminary studies, it is suggested that the Mollii suit improves spasticity. Recent studies also proposed that it improves mobility, gait, function and quality of life. However, these studies are based on qualitative and subjective measures.

Locations

Country	Name	City	State
Singapore	KKWCH	Singapore

Sponsors (2)

Lead Sponsor	Collaborator
KK Women's and Children's Hospital	Inerventions AB

Country where clinical trial is conducted

Singapore, 

References & Publications (2)

Mills PB, Dossa F. Transcutaneous Electrical Nerve Stimulation for Management of Limb Spasticity: A Systematic Review. Am J Phys Med Rehabil. 2016 Apr;95(4):309-18. doi: 10.1097/PHM.0000000000000437. Review. — View Citation

Wright PA, Durham S, Ewins DJ, Swain ID. Neuromuscular electrical stimulation for children with cerebral palsy: a review. Arch Dis Child. 2012 Apr;97(4):364-71. doi: 10.1136/archdischild-2011-300437. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Gait Profile Score (GPS)	GPS is a single index measure that summarises the overall deviation of kinematic gait data relative to normative data. It ranges from 0 to 30, the higher the score, the more severe the gait. We will measure change in GPS pre and post intervention.	1 month post intervention
Primary	Change in Gait Profile Score (GPS)	GPS is a single index measure that summarises the overall deviation of kinematic gait data relative to normative data. It ranges from 0 to 30, the higher the score, the more severe the gait. We will measure change in GPS pre and post intervention.	2 months post intervention
Primary	Change in Gait deviation index (GDI)	GDI provides a numerical value that expresses overall gait pathology (ranging from 0 to 100, where 100 indicates the absence of gait pathology). The higher the GDI, the better the result.	1 month post intervention
Primary	Change in Gait deviation index (GDI)	GDI provides a numerical value that expresses overall gait pathology (ranging from 0 to 100, where 100 indicates the absence of gait pathology). The higher the GDI, the better the result.	2 months post intervention
Primary	Change in Gait speed (metre/sec)	The faster the gait speed, the better the result.	1 month post intervention
Primary	Change in Gait speed (metre/sec)	The faster the gait speed, the better the result.	2 months post intervention
Primary	Change in Cadence (steps/ minute)	The higher the cadence, the better the result.	1 month post intervention
Primary	Change in Cadence (steps/ minute)	The higher the cadence, the better the result.	2 months post intervention
Secondary	Change in Gross motor function measure (GMFM)	GMFM is an assessment tool designed and evaluated to measure changes in gross motor function with intervention in children with cerebral palsy. The closer the score to 100%, the better the score.	1 month post intervention
Secondary	Change in Gross motor function measure (GMFM)	GMFM is an assessment tool designed and evaluated to measure changes in gross motor function with intervention in children with cerebral palsy. The closer the score to 100%, the better the score.	2 months post intervention
Secondary	Change in Functional Assessment Questionnaire (FAQ)	FAQ is a 10 point scale (with 10 being most able) which was designed specifically to be used as an outcome measure in individuals with physical disability. The higher the score the better the result.	1 month post intervention
Secondary	Change in Functional Assessment Questionnaire (FAQ)	FAQ is a 10 point scale (with 10 being most able) which was designed specifically to be used as an outcome measure in individuals with physical disability. The higher the score the better the result.	2 months post intervention
Secondary	Change in EQ5D	EQ5D is a standardised measure of health status to provide a simple, generic measure of health for clinical and economic appraisal. The descriptive system comprises 5 dimensions. Score ranges from 5 to 15. The higher score the poorer the result. The EQ VAS records the respondent's self-rated health on a vertical, visual analogue scale 0-100. The higher the score, the better the self-rated health.	1 month post intervention
Secondary	Change in EQ5D	EQ5D is a standardised measure of health status to provide a simple, generic measure of health for clinical and economic appraisal. The descriptive system comprises 5 dimensions. Score ranges from 5 to 15. The higher score the poorer the result. The EQ VAS records the respondent's self-rated health on a vertical, visual analogue scale 0-100. The higher the score, the better the self-rated health.	2months post intervention
Secondary	Change in ICF-CY ratings	The WHO International Classification of Functioning, Disability and Health, Children & Youth version (ICF-CY) is a measure to grade function of activities of daily living (ADLs). Few ICF-CY categories have been selected and graded based on the frequency, intrusiveness or severity of the specific impairment. In each category, rating ranges from 0 to 4. The higher the rating, the worse the outcome.	1 month post intervention
Secondary	Change in ICF-CY ratings	The WHO International Classification of Functioning, Disability and Health, Children & Youth version (ICF-CY) is a measure to grade function of activities of daily living (ADLs). Few ICF-CY categories have been selected and graded based on the frequency, intrusiveness or severity of the specific impairment. In each category, rating ranges from 0 to 4. The higher the rating, the worse the outcome.	2 months post intervention
Secondary	Compliance	Compliance is measured using log of use of mollii suit.	1 month post intervention
Secondary	Compliance	Compliance is measured using log of use of mollii suit.	2 months post intervention
Secondary	Acceptance	Acceptance to the mollii suit is evaluated qualitatively using an open-ended questionnaire filled up by patient and caregivers	1 month post intervention
Secondary	Acceptance	Acceptance to the mollii suit is evaluated qualitatively using an open-ended questionnaire filled up by patient and caregivers	2 months post intervention