UCL GOS Institute of Child Health
London, WC1N 1EH, United Kingdom
Location status: Recruiting
Location contact
Anna Kolesnik, PhD
CONTACT
David Skuse, Professor
CONTACT
Francesco Muntoni, Professor
CONTACT
Natasha Aslam, MSc
CONTACT
NCT Number: NCT06581887
Study aims to develop and to evaluate the neurophysiological and physiological response to a classical conditioning task.To better understand how Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) impacts mental health and how to assess it. Participants invited to complete questionnaires about behaviour, cognitive function and social interactions, complete computer tasks and have an optional MRI brain scan,
Interested in participating?
Request Info7 year–17 year
Male
Observational
London, WC1N 1EH, United Kingdom
Location status: Recruiting
Anna Kolesnik, PhD
CONTACT
David Skuse, Professor
CONTACT
Francesco Muntoni, Professor
CONTACT
Natasha Aslam, MSc
CONTACT
The investigation aims to develop and to evaluate the neurophysiological and physiological response to a classical conditioning task, which is comparable to findings that have been made in the mdx dystrophic mouse (deficient in Dp427). The investigators will assess correlations between the specific DMD/BMD genotype and susceptibility to conditioning, as well as the relationship between conditioning and behavioural/emotional characteristics of the syndrome. At the end of the study, the objective is to deliver a comprehensive test battery that is suitable for use in a trial of AON delivery to improve brain function.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
BMD patients:
Control participants:
Exclusion criteria
Control participants:
General exclusion criteria for MRI:
To evaluate the neurophysiological and physiological response to a classical conditioning task, which is comparable to findings that have been made in the mdx dystrophic mouse (deficient in Dp427). The investigators will assess correlations between the specific DMD/BMD genotype and susceptibility to conditioning, as well as the relationship between conditioning and behavioural/emotional characteristics of the syndrome.
Time frame: through study completion, an average of 2 years
Following an emotional response task, an interim analysis will be done after the first 30 patients have been tested (10 DMD, 10 BMD, 10 controls). A favourable outcome will demonstrate a difference in the emotional response of these groups. Groups will complete questionnaires, an emotional response task, and a fine motor assessment.
Time frame: through study completion, an average of 2 years
This will be measured by analysis measuring any difference between and within groups (10 BMD, 10 DMD and 10 control). Physiological responses generated by the task will be measured, along with neural imaging.
Contact information is provided by the study sponsor or research team.
Anna Kolesnik, Dr
CONTACT
Natasha Aslam, MSc
CONTACT
University College, London
Other
Acronym: D-BRAIN
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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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