rTMS Treatment of Spasticity in Children With Cerebral Palsy - a RCT

Sponsor
The University of Hong Kong (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06128746
Collaborator
(none)
20
2
20

Study Details

Study Description

Brief Summary

This RCT aims to investigate the effect of repetitive transcranial magnatic stimulation (rTMS) in treating children with hemiplegoc cerebral palsy. The study will measure any improvement in spasticity after using contra-lesional inhibitory rTMS follow by intensive limb training.

Participants will attend a 10-day rTMS treatment sessions, follow by intensive training of the impaired limb. They will also undergo MRI scans before and after the treatment to investiagte the underlying neurophysiological mechanisms that lead to changes clinically by using TMS as well as MR-DKI. Researchers will compare the intervention group and the sham group to see if rTMS could result in improvement of participants' spasticity.

Condition or Disease Intervention/Treatment Phase
  • Device: Repetitive Transcranial Magnetic Stimulation
  • Device: Sham Repetitive Transcranial Magnetic Stimulation
N/A

Detailed Description

Cerebral palsy is the most common cause of lifelong physical disability in childhood, with an estimated prevalence of 1.5 per 1000 living biths for primary school-aged children. Spasticity is the most common symptoms in children with cerebral palsy, leading to muscle weakness affecting gross motor functions and causing complications such as pain, contracture and subluzation which will lead to inability to perform activity-based training and subsequently lead to further muscle weakness. Standard therapy with regular physiotherapy and occupational therapy are essential but time-consuming and the effects might not last for longer duration. Patients or caregivers decline medications because of side effects drowsiness while other interventions such as intra-thecal baclofen pump, rhizotomy or surgery are invasive.

Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive brain stimulation technique that has the ability to modulate excitation of the motor cortex area of the brain. There were past studies suggesting that using contralesional inhibitory rTMS was safe and feasible for patients with paediatric subcortical stroke and seemed to improve hand function in patients with hemiparesis. However, limited studies have been published on the effects of rTMS on improving spasticity in children with cerebral palsy. Hence, the objective of this study is to use low-frequency rTMS to the contra-lesional hemisphere in children with hemiplegic cerebral palsy to investigate if rTMS follow by intensive limb training would improve spasiticity of these children and whether the improvement can be sustained for a longer time. The underlying mechanisms that lead to the changes clinically will also be investigated by TMS and MRI.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Repetitive Transcranial Magnetic Stimulation (rTMS) for the Treatment of Spasticity in Children With Hemiplegic Cerebral Palsy - a Randomized Controlled Trial
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
May 1, 2025
Anticipated Study Completion Date :
Jul 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Interventional rTMS group

The intervention group will receive 1 Hz active rTMS during treatment, lasting for 20 minutes, follow up by 30 minutes of intensive limb training.

Device: Repetitive Transcranial Magnetic Stimulation
1 Hz rTMS treatment for 20 mins, follow by 30 mins intensive limb training

Sham Comparator: Sham rTMS group

The sham group will not receive any Hz of rTMS during treatment, also lasting for 20 minutes with 30 minutes of intensive limb training afterwards.

Device: Sham Repetitive Transcranial Magnetic Stimulation
Sham Hz rTMS treatment for 20 mins, follow by 30 mins intensive limb training

Outcome Measures

Primary Outcome Measures

  1. Modified Ashworth Scale [Day 10, 17 of intervention and 2 months post intervention]

    Clinical measure of spasticity. Scores range from 0 to 4, with a higher score indicate worse in muscle tone

  2. The range of motion scores [Day 10, 17 of intervention and 2 months post intervention]

    ROM of thumb adduction, wrist dorsal flexion and extension, and elbow dorsal flexion and extension. Patients' range of motion score will be compared to the normative values

Secondary Outcome Measures

  1. Zancolli scale [Day 10, 17 of intervention and 2 months post intervention]

    Severity of forearm alignment. Scores range from 0 to 3 with a higher score indicate worse hand function

  2. House functional classification scale [Day 10, 17 of intervention and 2 months post intervention]

    Rating of functional use of the impaired upper limb. Scale consists of nine grades from 0 (does not use) to 8 (full spontaneous use)

  3. Gross motor function measure [Day 10, 17 of intervention and 2 months post intervention]

    Changes in motor function. A 4-point Likert scale with higher score indicates better motor function

  4. Assisting hand assessment [Day 10, 17 of intervention and 2 months post intervention]

    Test of hand function

  5. Pediatric Quality of Life Cerebral Palsy module [Day 10, 17 of intervention and 2 months post intervention]

    Quality of life measurement. Scores range from 0 to 100 with higher score indicate better quality of life.

  6. MRI Brain: fMRI and DKI [Day 10, 17 of intervention and 2 months post intervention]

    Functional MRI and Diffusion Kurtosis Imaging measuring the brain microstructural changes and structural connectivity during the intervention

Eligibility Criteria

Criteria

Ages Eligible for Study:
7 Years to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients aged between 7 years and 18 years

  • Diagnosis of cerebral palsy with hemiplegia

  • Upper limb spasticity ≥ 1

  • IQ ≥ 50

Exclusion Criteria:
  • Any contra-indications to rTMS

  • Severe spasticity (score of 4 or more in Ashworth scale)

  • Uncontrollable epilepsy

  • History of Botulinum toxin A injection in previous 6 months

  • Upper limb casting in previous 6 months

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • The University of Hong Kong

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Winnie Wan Yee Tso (Dr), Clinical Assistant Professor, The University of Hong Kong
ClinicalTrials.gov Identifier:
NCT06128746
Other Study ID Numbers:
  • rTMSCPHKU
First Posted:
Nov 13, 2023
Last Update Posted:
Nov 13, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Winnie Wan Yee Tso (Dr), Clinical Assistant Professor, The University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 13, 2023