Active Transcranial Direct Current Stimulation
DeviceParticipants will receive 20 min of tDCS over the scalp during 20 min of motor training.
NCT Number: NCT04725019
The goal of this study is to test the effects of transcranial direct current stimulation (tDCS) on motor learning and brain plasticity in children with unilateral spastic cerebral palsy (USCP).
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Notify Me6 year–17 year
All sexes
Interventional
Not applicable
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Children between 6-17 years old who have been diagnosed with cerebral palsy, with the following joint mobility: wrist extension 20º, metacarpophalangeal and proximal interphalangeal joints 10º. Ability to cooperate and follow simple directions.
Exclusion criteria
Participants will receive 20 min of tDCS over the scalp during 20 min of motor training.
Participants will engage in a high number of repetition of movements that use both hands while playing with toys and games. Training will be provided 20 min/day, for 5 consecutive days.
Time frame: Day before intervention begins, compared to day after intervention ends (approximately 1 week)
Investigators will measure changes in how well the child uses both hands cooperatively for bimanual activities.
Time frame: Day before intervention begins, compared to day after intervention ends (approximately 1 week)
Investigators will measure changes in the movement speed of the hands.
Time frame: Day before intervention begins, compared to day after intervention ends (approximately 1 week)
Investigators will measure change in measurements of cortical excitability using transcranial magnetic stimulation (TMS) from baseline to follow-up (1 week).
Boston University Charles River Campus
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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