Priming Effects of Ultra-high Frequency Quattro Pulse Transcranial Brain Stimulation Prior to Hand Motor Function Training in Children With Unilateral Spastic Cerebral Palsy (TRAINCP)
Primary Purpose
Cerebral Palsy, Spastic, Transcranial Magnetic Stimulation, Repetitive
Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Quadri-pulse theta burst stimulation
Sponsored by
About this trial
This is an interventional treatment trial for Cerebral Palsy, Spastic focused on measuring Unilateral Spastic Cerebral Palsy, Cortico-spinal Reorganization, Transcranial Magnetic Stimulation, Sham-controlled Trial, Intensive Hand Function Training
Eligibility Criteria
Inclusion Criteria:
- Assured diagnosis of USCP.
- Children aged 6 to 18 years with USCP
- Dated and signed informed consent of legal guardian, informed assent from minor
Exclusion Criteria:
- Epilepsy
- Implanted shunt system
- If singular primary motor cortex cannot be identified by TMS, e.g. because of bilateral cortico-spinal reorganization or resting motor threshold above 80% maximum stimulator output (MSO)
- Chronic medication acting on the central nervous system
- Severe mental retardation
- Psychiatric diseases
- Pregnancy
- Uncooperative patients
Sites / Locations
- Technical University MunichRecruiting
- Clinic for Neuropediatrics and Neurorehabilitation, Epilepsy Center for Children and Adolescents, Schön KlinikRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Intervention
Sahm-control
Arm Description
Real transcranial magnetic stimulation applied
Sham transcranial magnetic stimulation applied
Outcomes
Primary Outcome Measures
Assisting hand assessment
Difference in change of logit assisting hand assessment scores between the TMS and sham-TMS group from baseline to end of 10 days intensive hand function training.
Secondary Outcome Measures
Corticospinal reorganization
Subgroup analyses of the primary endpoint (cortico-spinal organization, age and sex) will be computed.
Assisting hand assessement - smallest detectable difference
Number of patients per treatment group who achieved the smallest detectable difference in logit assisting hand assessment score of 5 points at visit 12.
Assisting hand assessement - Follow up
Difference in the assisting hand assessment logit score between the TMS and sham-TMS group 12 months after the standardized hand motor function training.
Neuronal plasticity
Differences in neuronal plasticity as measured by motor evoked potentials with suprathreshold TMS single pulses between baseline and visit 12 as well as after 12 months follow-up.
Box-and-blocks test
Differences of Blocks transferred with the Box-and-blocks test between the TMS and sham-TMS group between baseline and visit 12 as well as after 12 months follow-up
Goal attainment scaling
Differences in Goal Attainment Scaling between the TMS and sham-TMS group between baseline and visit 12 as well as after 12 months follow-up.
Canadian occupational performance measure
Differences in the Canadian Occupational Performance Measure scale between the TMS and sham-TMS group between baseline and visit 12 as well as after 12 months follow-up.
Full Information
NCT ID
NCT05165472
First Posted
December 7, 2021
Last Updated
June 26, 2023
Sponsor
Technical University of Munich
Collaborators
German Federal Ministry of Education and Research
1. Study Identification
Unique Protocol Identification Number
NCT05165472
Brief Title
Priming Effects of Ultra-high Frequency Quattro Pulse Transcranial Brain Stimulation Prior to Hand Motor Function Training in Children With Unilateral Spastic Cerebral Palsy
Acronym
TRAINCP
Official Title
Priming Effects of Ultra-high Frequency Quattro Pulse Transcranial Brain Stimulation Prior to Hand Motor Function Training in Children With Unilateral Spastic Cerebral Palsy
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2022 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
June 30, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Technical University of Munich
Collaborators
German Federal Ministry of Education and Research
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Unilateral spastic cerebral palsy (USCP) leads to life-long impairment with a hemiparesis of the affected side of the body. Rehabilitation efforts combine evidence based methods such as constrained induced movement therapy (CIMT) or hand-arm bimanual intensive therapy (HABIT) as well as training in daily life activities and psychological support in order to improve participation. It has been tried to enhance hand motor function trainings with non-invasive brain stimulation. However, evidence of this promising approach is limited. This might be due to a non-consideration of the individually different types of cortico-spinal projections to the paretic hand that demonstrated to be of highly relevant for the therapy of these children. Approximately one third of such patients control their paretic hands via crossed projections from the affected hemisphere (CONTRA), while one third uses ipsilateral projections from the contralesional hemisphere (IPSI). This study aims - for the first time - to enhance the effects of the training by priming the primary motor cortex (M1) of the paretic hand with a newly established high frequency quadri-pulse theta burst stimulation (qTBS) in a randomized, patient and evaluator blind, sham-controlled approach, for the first time taking the individual type of cortico-spinal reorganization (CONTRA vs IPSI) into account. This promising and neurophysiologically motivated approach is likely to ameliorate hand function in children with USCP.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy, Spastic, Transcranial Magnetic Stimulation, Repetitive
Keywords
Unilateral Spastic Cerebral Palsy, Cortico-spinal Reorganization, Transcranial Magnetic Stimulation, Sham-controlled Trial, Intensive Hand Function Training
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized, sham-controlled, patient- and evaluator-blind, two-centre, parallel group study
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
32 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Real transcranial magnetic stimulation applied
Arm Title
Sahm-control
Arm Type
Sham Comparator
Arm Description
Sham transcranial magnetic stimulation applied
Intervention Type
Other
Intervention Name(s)
Quadri-pulse theta burst stimulation
Intervention Description
High frequency transcranial quadri-pulse theta burst stimulation prior to hand motor function training
Primary Outcome Measure Information:
Title
Assisting hand assessment
Description
Difference in change of logit assisting hand assessment scores between the TMS and sham-TMS group from baseline to end of 10 days intensive hand function training.
Time Frame
10 days
Secondary Outcome Measure Information:
Title
Corticospinal reorganization
Description
Subgroup analyses of the primary endpoint (cortico-spinal organization, age and sex) will be computed.
Time Frame
1 year
Title
Assisting hand assessement - smallest detectable difference
Description
Number of patients per treatment group who achieved the smallest detectable difference in logit assisting hand assessment score of 5 points at visit 12.
Time Frame
1 year
Title
Assisting hand assessement - Follow up
Description
Difference in the assisting hand assessment logit score between the TMS and sham-TMS group 12 months after the standardized hand motor function training.
Time Frame
1 year
Title
Neuronal plasticity
Description
Differences in neuronal plasticity as measured by motor evoked potentials with suprathreshold TMS single pulses between baseline and visit 12 as well as after 12 months follow-up.
Time Frame
1 year
Title
Box-and-blocks test
Description
Differences of Blocks transferred with the Box-and-blocks test between the TMS and sham-TMS group between baseline and visit 12 as well as after 12 months follow-up
Time Frame
1 year
Title
Goal attainment scaling
Description
Differences in Goal Attainment Scaling between the TMS and sham-TMS group between baseline and visit 12 as well as after 12 months follow-up.
Time Frame
1 year
Title
Canadian occupational performance measure
Description
Differences in the Canadian Occupational Performance Measure scale between the TMS and sham-TMS group between baseline and visit 12 as well as after 12 months follow-up.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Assured diagnosis of USCP.
Children aged 6 to 18 years with USCP
Dated and signed informed consent of legal guardian, informed assent from minor
Exclusion Criteria:
Therapy refractory epilepsy
Seizures within the last 2 years
More than 1 anti epileptic drugs
Implanted shunt system
If singular primary motor cortex cannot be identified by TMS, e.g. because of bilateral cortico-spinal reorganization or resting motor threshold above 80% maximum stimulator output (MSO)
Severe mental retardation
Psychiatric diseases
Pregnancy
Uncooperative patients
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Volker Mall, Prof.
Phone
+49 (0)89 71009-233
Email
volker.mall@kbo.de
First Name & Middle Initial & Last Name or Official Title & Degree
Nikolai Jung, PD Dr. med
Phone
+49 (0)89 71009-236
Email
nikolai.jung@tum.de
Facility Information:
Facility Name
Technical University Munich
City
Munich
ZIP/Postal Code
81377
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Volker Mall, Prof.
Phone
+49 (0)89 71009-233
Email
volker.mall@kbo.de
First Name & Middle Initial & Last Name & Degree
Nikolai Jung, Dr.
Phone
+49 (0)89 71009-236
Email
nikolai.jung@tum.de
Facility Name
Clinic for Neuropediatrics and Neurorehabilitation, Epilepsy Center for Children and Adolescents, Schön Klinik
City
Vogtareuth
ZIP/Postal Code
83569
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Steffen Berweck, Prof.
Phone
+49 (0)8038 901418
Email
sberweck@schoen-kliniken.de
First Name & Middle Initial & Last Name & Degree
Julia Hartmann
Phone
+49 (0)8038 901418
Email
JHartmann@schoen-klinik.de
12. IPD Sharing Statement
Plan to Share IPD
Undecided
IPD Sharing Plan Description
Sharing upon request planned
Learn more about this trial
Priming Effects of Ultra-high Frequency Quattro Pulse Transcranial Brain Stimulation Prior to Hand Motor Function Training in Children With Unilateral Spastic Cerebral Palsy
We'll reach out to this number within 24 hrs