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Mechanism of Action of Transcranial Direct Current Stimulation in Neurofibromatosis Type 1

Not Applicable
Completed
Conditions
Neurofibromatosis 1
Interventions
Other: Transcranial direct current stimulation
Registration Number
NCT04991428
Lead Sponsor
University of Manchester
Brief Summary

Intellectual impairment, particularly working memory deficits are a significant cause of morbidity in children with Neurofibromatosis type (NF1) with long-term implications on academic and occupational functioning. Whilst significant discoveries have been made in Nf1 animal models in trying to find treatments for these conditions, human translational studies have not been successful. This mechanistic experimental study will investigate the neural mechanisms underlying working memory deficits in NF1. In particular, we will investigate how individual differences in inhibitory neurotransmitter GABA relate to performance on working memory tests. Further, we will investigate the use of a novel, experimental intervention called transcranial Direct Current Stimulation (tDCS);known to modulate GABA. Using a randomized, crossover design in a cohort of 30 adolescents aged 11-17 years, we will apply real or sham tDCS to the dorsolateral prefrontal cortex (DLPFC). State-of-art real time imaging techniques such as Magnetic Resonance Spectroscopy (MRS) and task based functional MRI (fMRI) will be used to investigate the effect of tDCS on GABA concentration, changes in functional plasticity and working memory. We expect that results from this study will help elucidate the neural mechanisms underlying working memory deficits in people with NF1 and show biologic activity for a novel, low-cost intervention that can be used for cognitive remediation in NF1. This kind of focused mechanism trial method is a highly promising approach to understanding the complex neural system pathology in a multifactorial neurodevelopmental condition like NF1.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
31
Inclusion Criteria
  1. Meets National Institute of Health NF1 diagnostic criteria
  2. Children aged 11-17 years
  3. Written informed consent/assent
Exclusion Criteria
  1. No history of intracranial pathology other than asymptomatic optic pathway glioma or other asymptomatic and untreated NF1-associated white matter lesion
  2. No history of epilepsy or any major mental illness
  3. No MRI contraindications.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Sham stimulationTranscranial direct current stimulationSimilar set-up but no actual stimulation
Active trancranial direct current stimulationTranscranial direct current stimulationActive stimulation for 15 minutes
Primary Outcome Measures
NameTimeMethod
Corsi Block taskimmediately after the intervention

memory span task

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Manchester

🇬🇧

Manchester, Greater Manchester, United Kingdom

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