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NCT06874166Not yet recruiting

Social Cognition in Dystrophinopathies and Neurodevelopmental Disorders

Social Cognition in Dystrophinopathies and Neurodevelopmental Disorders. Behavioural and Psychophisiological Measures

Source: ClinicalTrials.gov · Last updated 13 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The primary aim of this observational study is to investigate specific aspects of social cognition in dystrophinopathies. Body awareness, interpersonal distance and emotional processing will be measured in a sample of patients affected by Becker (BMD) and Duchenne (DMD) muscular dystrophy, compared with a sample of patients affected by osteogenesis imperfecta (OI), and both compared with a control sample with typical development. The secondary aim is to study cortical activity at rest, by means of electroencephalography (EEG), to explore frequencies and time course of EEG responses. Moreover, the relationship between EEG activity and neuropsychological, dispositional and subjective measures will be explored through correlational analyses.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
45 (estimated)
First submitted
17 Feb 2025
Start date
Sept 2025
Primary completion date
Sept 2027
Lead sponsor
IRCCS Eugenio Medea
NCT number
NCT06874166

What you commit to

  • Study type: Observational
  • Planned participants: 45
  • From Sept 2025 to the primary completion date, Sept 2027
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • specific condition that could prevent the application of the tests and tasks under study, such as: a) the need for PEG; b) the need for tracheostomy; c) the need for assisted ventilation.

Other

  • presence of comorbid diagnoses,
  • sensory deficit
  • cognitive level lower than 60.

Who the study is looking for

  • Patients diagnosed with Duchenne and Becker muscular dystrophy (genetic and histological diagnosis and clinical diagnosis) (ambulant and non-ambulant).
  • Patients diagnosed with osteogenesis imperfecta.
  • Control group: participants without any neurological or psychiatric disorder

Age in the registry: 4 years to - · Sex: Male · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.