Clinical trials

33

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Condition / disease
Location
Status: Recruiting

Clinical Improvement Due to the Home Use of Agilik in Children With Cerebral Palsy

The goal of this clinical trial is to learn if a two month training with the Agilik powered orthosis improves the knee extension or the endurance in pediatric patients with Cerebral palsy and a crouch gait. It will also learn about the safety of Agilik. The main questions it aims to answer are: Does the Agilik powered orthosis increase the value of the knee extension during walking? What medical problems do participants have when using the Agilik powered orthosis? Researchers will compare a group of patients using the Agilik powered exoskeleton with a group of patients treated with standard therapy. Participants will: Use Agilik at home or perform standard therapy for 2 months Visit the clinic at the beginning of the study, after 3 months and after 1 additional month.

Participants needed: 40
Trial details
Age: 5-17Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Jun 26, 2026Locations: 6
Eligibility criteria

Diagnosis of CP and a crouch gait [+9]

Any severe neurological, musculoskeletal and/or cardiorespiratory involvement pr... [+3]

Status: Not yet recruiting

AI-based Model for Rehabilitation Engagement and Motor Performance Evaluation in Pediatric Patients: A Pilot Study

What is the purpose of this study? This study aims to evaluate the usability and feasibility of an artificial intelligence-based model designed to monitor in real-time the engagement and motor performance of pediatric patients during technology-assisted rehabilitation. Who can take part? 15 participants between 5 and 17 years old with neuromotor impairments will take part, along with at least 5 of their referring physiotherapists. What will happen in the study? Each pediatric patient will take part in a single, 1-hour rehabilitation session using either the Lokomat or GRAIL system, according to their standard clinical prescription. During the session, the physiotherapist will have access to a display showing real-time data from the AI model, including the patient's heart rate, engagement level, pleasantness, activation, and motor performance. At the end of the session, the physiotherapist will complete a System Usability Scale (SUS) questionnaire and provide direct feedback on how to improve the model. Why is this study important? Assessing the usability of this real-time monitoring tool is a necessary step to understand if it is practical for clinical use. Providing therapists with objective, real-time insights into a child's psychological and physical state can ultimately help tailor therapy to the specific needs of each patient, improving the overall rehabilitation experience.

Participants needed: 15
Trial details
Age: 5-17Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Subjects aged between 5 and 17 years with neuromotor impairments who are undergo...

Uncooperative subjects.

Status: Recruiting

I-TOPS With Patients With Genetic Syndrome SYN-TOPS

Genetic syndromes involving the central nervous system are often associated with cognitive, behavioral and communication difficulties that negatively impact adaptive functioning and quality of life. Despite advances in digital health, there remains a lack of evidence-based interventions targeting executive functions and psychosocial outcomes in this population. This multicenter study aims to evaluate the feasibility and efficacy of an adapted version of the Teen Online Problem-Solving (TOPS) program, a web-based intervention designed to enhance problem-solving, self-regulation and communication skills in everyday contexts. The adapted intervention (I-TOPS) will be tailored for adolescents and young adults with genetic syndromes involving the central nervous system. The I-TOPS intervention requires the participation of both the adolescent/young adult and at least one parent, caregiver or legal guardian, as it is a family-centered program. Participants will complete online modules at home, supported by bimonthly videoconference sessions with a cognitive-behavioral psychologist. Outcomes will be assessed through pre- and post-intervention measures of executive functioning, adaptive behavior and psychological well-being, reported by both participants and caregivers. Psychological well-being of participating parents/caregivers/guardians will also be evaluated. The study aims to provide evidence for an accessible, scalable telehealth intervention to improve cognitive and behavioral outcomes in this underserved population.

Participants needed: 42
Trial details
Age: 11-39Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: May 1, 2026Locations: 1
Eligibility criteria

Diagnosis of genetic syndrome [+4]

Presence of severe or profound intellectual disability; [+2]

Status: Not yet recruiting

Transdiagnostic Dimensional Profiling of Neurodevelopmental Disorders

In recent years, the growing awareness of the multifactorial nature of neurodevelopmental disorders has stimulated interest in transdiagnostic approaches aimed at investigating underlying etiological mechanisms beyond traditional diagnostic categories. In this context, the present study seeks to provide a transdiagnostic profiling of both domain-general cognitive functions (attention, working memory, executive control) and domain-specific functions (phonological awareness, rapid naming, vocabulary, reading) underlying the main neurodevelopmental disorders in a large sample of preschool and school-age children (3-11 years), through the use of CRAB (Computerized Reading-related Assessment Battery). CRAB is a digital platform specifically developed by SUPSI and the Université de Genève to integrate, within a single testing environment, the assessment of the main domain-general and domain-specific cognitive functions underlying neurodevelopmental disorders. In particular, participating families will receive an email containing a link to access the CRAB platform, which will not include their personal data but rather a code provided by the staff of IRCCS Medea. A screen will open displaying several game-like tasks designed to measure both domain-general and domain-specific cognitive functions, which must be completed by the participating subject. The main objective is to obtain a fine-grained and multidimensional mapping of cognitive profiles prior to the standard diagnostic process, in order to identify early patterns of (a)typical or at-risk functioning.

Participants needed: 300
Trial details
Age: 3-11Biological sex: AllType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: Apr 22, 2026Duration: 6 Months
Eligibility criteria

Age between 3 and 11 years; [+4]

Age outside the specified range; [+5]

Status: Recruiting

Cortical Tracking of Speech in the First Year of Life

The goal of this observational study is to investigate early neural mechanisms underlying the processing of spoken language, specifically the phenomenon of cortical tracking, and to determine whether these mechanisms can serve as early predictors of later language development outcomes in infants, including both typical and atypical trajectories. The main questions it aims to answer are: * How do infants with and without a familial history of language and learning impairments differ in their neural ability to track speech and non-speech auditory stimuli at an early stage of development (around 8 months of age)? * To what extent do early cortical tracking mechanisms predict later language abilities, including both receptive and expressive skills, measured at approximately 18 months of age? Researchers will compare infants with a familial risk for language and learning impairments (FH+) to infants without such risk (FH-) to determine whether differences in early neural processing of auditory stimuli are associated with later language outcomes. Participants will: * undergo a neurophysiological assessment involving non-invasive electroencephalographic (EEG) recording while being exposed to auditory stimuli, including: speech stimuli (pre-recorded simple stories in Italian, presented in infant-directed speech); non-speech stimuli (musical sounds matched for rhythmic and acoustic properties) * take part in a developmental assessment at approximately 8 months of age, including standardized measures of cognitive and early linguistic abilities * be involved in a follow-up assessment approximately 10 months later (around 18 months of age), during which standardized tests will evaluate language comprehension and production abilities * have additional background information collected, including family history of language and learning disorders and socio-demographic characteristics, to better understand potential risk and protective factors The study follows a longitudinal design and uses non-invasive procedures that do not require active responses from the infant.

Participants needed: 50
Trial details
Age: 30-34Biological sex: AllType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: Apr 15, 2026Locations: 1
Eligibility criteria

Healthy infants aged between 7 and 8 months [+2]

Gestational age < 37 weeks and/or birth-weight < 2500 grams [+3]

Status: Recruiting

Sleep Disturbance in Subjects With Autism Spectrum Disorders (ASD) in Preschool Age (18-60 Months)

An observational study is one that aims to collect data from routine clinical practice, without altering a patient's standard diagnostic and therapeutic pathway (no additional instrumental or laboratory tests beyond those performed in clinical practice are envisaged). The overall objective of this study is to investigate sleep disorders in preschool-aged children with Autism Spectrum Disorder. Sleep plays a key role in early brain development. The prevalence of sleep disorders in childhood is reported to be between 10 and 50%, with a prevalence of up to 86% in children with neurodevelopmental disorders. Over the past few decades, numerous studies have demonstrated a significant bidirectional connection between sleep problems and various areas of child development. Therefore, early identification of sleep disorders in childhood is essential for adequate treatment and prevention of negative cognitive and socioemotional impacts. Recent studies have demonstrated a hypothetical role for vitamin D and iron in regulating sleep. The objectives of the study are to describe sleep disturbances in a group of preschool-aged subjects with ASD (18-60 months), to measure blood ferritin and vitamin D levels, and to assess a possible correlation with specific subtypes of sleep disturbances. Given the impact that sleep disturbances have on various areas of children's development, secondary objectives include assessing a possible positive correlation between the severity of sleep disturbances and symptoms related to Autism Spectrum Disorder and/or other psychiatric comorbidities.

Participants needed: 200
Trial details
Age: 18-60Biological sex: AllType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: Mar 24, 2026Locations: 2
Eligibility criteria

Subjects with ASD [+1]

Status: Recruiting

Implementation and Validation of Instrumented Stair Climb Test

The aim of this study is to design an instrumented test for the evaluation of the climb of stairs. In particular, the main purpose is to characterize and compare the performance of subjects, both pediatrics and adults, with different pathologies (cerebral palsy, amputee, Parkinson's disease, stroke and arthroplasty) in carrying out the instrumented test of climbing and descending stairs. This would provide potentially useful information to complement the clinical assessment, including investigating the existence of correlations between the instrumental data obtained and the clinical scales collected. The secondary objective is to evaluate, in a first phase of the study, the feasibility and reliability of the test, analyzing the validity of the indices obtained in terms of intra- and inter-operator reliability on healthy subjects.

Participants needed: 64
Trial details
Age: 4-80Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Feb 27, 2026Locations: 3
Eligibility criteria

Need for help from an operator or use of orthoses to make the stairs; [+18]

Status: Recruiting

Antenatal Stress and Infants In MAR

The goal of this observational longitudinal study is to examine the association between prenatal psychological and biological stress and neonatal health outcomes in couples who conceived through medically assisted reproduction. The study includes expectant mothers and fathers during pregnancy and at birth and focuses on pregnancies achieved through homologous fertilization and heterologous fertilization via oocyte donation. The main questions this study aims to answer are: 1. How do psychological and biological indicators of stress manifest during pregnancy in women who have undergone medically assisted reproduction? 2. Is prenatal maternal stress associated with neonatal health outcomes independently of genetic factors? 3. How does perceived stress present in expectant fathers during pregnancy? Researchers will compare couples who conceived through homologous fertilization with couples who conceived through heterologous fertilization via oocyte donation to understand whether associations between prenatal maternal stress and neonatal outcomes are independent of shared genetic background. Participants will: * Complete a remote eligibility assessment collecting information on pregnancy characteristics, parental health, and maternal psychological well-being * Complete online questionnaires at multiple time points during pregnancy and at birth assessing anxiety and depressive symptoms, perceived social support, and self-efficacy (both parents), as well as pregnancy-specific measures and prenatal bonding (mothers only) * In late pregnancy, mothers will collect saliva samples at home over two consecutive days to assess biological markers of stress (cortisol and alpha-amylase)

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: Feb 13, 2026Locations: 1
Eligibility criteria

Pregnant women in the first trimester and their respective partners. [+4]

Parents under 18 years of age. [+12]

Status: Recruiting

Characterization of (A)Typical Sensorimotor Pathways in Individuals With Autism

The goal of this interventional study is to understand whether sensorimotor skills could represent an endophenotype for autism, i.e. a specific class of biomarkers that bridges the gap between biological components of a condition and the behavioral/clinical dimensions. Motor and sensory differences are often observed in people with autism and may appear early in development or be shared among family members. The study will address three main questions: * What are the developmental effects of early differences in motor and sensory skills? * Are motor and sensory abilities influenced by family relationships? * Can studying motor and sensory differences in autism help researchers better understand the biological mechanisms underlying the condition? This study is structured in three topic-oriented work packages (WPs): WP1, a longitudinal assessment of sensorimotor skills as early predictors of later social characteristics in a mixed sample of infant siblings of autistic children (at elevated likelihood of autism) or with typical familial likelihood (no first-degree relatives with autism) (Q1); WP2, a cross-sectional investigation of sensorimotor abilities in autistic children and their parents as compared with typically developing children and their parents (Q2); and WP3, a dense-phenotyping approach to establish, within individuals, associations between traits across behavioral, neural, and molecular levels.

Participants needed: 300
Trial details
Age: 1+Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Feb 5, 2026Locations: 1
Eligibility criteria

children aged 2 to 12 years (both autistic and typically developing) [+3]

Presence of medical and/or neurological conditions of clinical significance, inc... [+2]

Status: Recruiting

Observational Study to Observe Variations of Gait Parameters in Patients With Neuromuscular Diseases

This study has the general objective of observing walking parameters during a clinical test to objectively estimate fatigue in patients with neuromuscular diseases. Furthermore, the investigators want to evaluate the feasibility of collecting physical activity in daily life conditions during a one-week monitoring period using a wearable sensor.

Participants needed: 120
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: Jan 20, 2026Locations: 2
Eligibility criteria

Ambulant adult patients with genetic diagnosis of muscular dystrophy/myopathy (d... [+1]

Dilated or ischemic heart disease with moderate impairment; [+1]

Status: Recruiting

Assessing Real Life Effectiveness of Treatment in Neurodevelopmental Disorders

The goal of this observational study is to learn if and how pharmacological and psychotherapeutic group treatments can treat clinical symptoms of children and adolescent patients with ADHD. The main questions it aims to answer are: * Are pharmacological and psychotherapeutic treatments effective on the clinical symptoms of patients with ADHD? * Are pharmacological and psychotherapeutic treatments effective on symptoms of emotion-behavioral dysregulation? * Is it possible to find associations between individual characteristics and treatment responses evaluating behavioral and neural correlates in children and adolescents with traits of emotion-behavioral dysregulation, externalizing disorders, and/or ADHD, using a panel of multimodal measures. May the data collected contribute to the definition of profiles useful for generating predictive hypotheses aimed at developing more personalized interventions? Researchers will compare the data collected from patients treated with pharmacological and psychotherapeutic group treatments with the data of subjects of comparable sex/gender, age, diagnoses, on the waiting list for treatment to see if pharmacological and psychotherapeutic treatments effects ADHD and emotional dysregulation symprtoms. Participants, patients who are offered treatment by clinicians according to standard clinical practice, will be asked to participate in the study by undergoing experimental assessments before and after the treatment. The multimodal panel of proposed assessments includes: * behavioral assessments, conducted through the completion of clinical and socio-demographic questionnaires; * neuropsychological assessments, conducted through standardized computerized neuropsychological tests; * neurophysiological assessments, conducted through the recording of NIRS (near infrared spectroscopy) and EEG (electroencephalogram) signals during an attentional task (Go-NoGo) and via a smartwatch.

Participants needed: 80
Trial details
Age: 8-15Biological sex: AllType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: Dec 9, 2025Locations: 1Duration: 9 Months
Eligibility criteria

Children and adolescents aged 8-15 years; [+2]

IQ < 75; [+7]

Status: Recruiting

Cortical Correlates of Spatial Navigation Skills in an Immersive Virtual Reality Environment

The goal of this study is to investigate the neural mechanisms that undergoes spatial navigation skills in children/adolescents aged between 8 and 17 years. These skills play an important role in daily life, as they allow us to orient ourselves in familiar and unfamiliar environments, locate objects, interact with them and memorize their position. Navigation abilities vary widely between individuals, change with age and might be affected by diseases, such as the cerebral palsy (CP). Previous studies have, in fact, demonstrated differences in the learning and adaptation methods of spatial navigation skills in children affected by CP compared to typically developing (TD) peers. Through the use of the electroencephalogram (EEG) we want to shed light on the mechanisms that govern this ability with the aim of: 1. better characterize spatial navigation skills in children/adolescents, both TD and affected by CP; 2. investigate the origin of the differences found between the spatial navigation skills of TD children and those affected by CP, improving knowledge of the pathology and thus allowing, in the future, to identify more adequate rehabilitation interventions.

Participants needed: 70
Trial details
Age: 8-17Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Nov 19, 2025Locations: 2
Eligibility criteria

typically developing subjects aged between 8 and 17 years; [+1]

subjects aged under 8 or over 17 years; [+3]

Status: Recruiting

Speech Therapy and Parenting for Early Socio-communicAtive sKills

Every year, millions of children are diagnosed with neurodevelopmental disabilities. This term covers a wide range of conditions, from genetic syndromes to brain injuries such as cerebral palsy. Children with neurodevelopmental disabilities often struggle in multiple areas, including language development. While standard speech therapy mainly focuses on understanding and producing words, these children may also have difficulties with the social and communicative skills needed for language. The parent-child relationship is especially important for helping kids develop in their early years. This clinical trial aims to find out if an intervention focused on early social and communication skills, and involving parents, can help children with neurodevelopmental disabilities. The study includes children aged 6 months to 5 years. It seeks to answer two key questions: * Does this intervention improve social and communication skills better than standard speech therapy? * Does this intervention affect how parents interact with their child? To find the answers, the study will compare two groups: one group will get the parent-involved intervention that focuses on early communication skills, while the other group will get standard speech therapy. In the first intervention, therapists will guide parents in observing and supporting their child's social and communication behaviors during various activities like playtime and snack time. In contrast, the standard speech therapy will focus on traditional goals, such as improving the child's ability to vocalize, understand, and use words, without involving parents. Both interventions will follow the same schedule-eight weekly sessions, each lasting 45 minutes, over two months. Before and after the interventions, the children and parents will: * Have an assessment of the child's language, social, and communication development. * Participate in a 10-minute video recording of parent-child playtime, which will be used to study parenting behavior.

Participants needed: 60
Trial details
Age: 6-59Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Nov 24, 2025Locations: 9
Eligibility criteria

Age between 6 months (corrected age in cases of prematurity) and 5 years. [+7]

Age greater than 5 years at the time of recruitment. [+6]

Status: Not yet recruiting

Transition to Adulthood in People With Muscular Dystrophy

The study will involve boys with Duchenne Muscular Dystrophy (DMD), from adolescence to adulthood living in Italy, and their families/ caregivers. The Investigators want to explore patients' mental health, social cognition and perception of body image as well as patients'and caregivers' ability to adapt to changes related to both the disease and various personal and social needs, through the use of short and simple questionnaires, neuropsychological tests and neurocognitive evaluation in ecological scenarios using Virtual Reality. The desire for autonomy and the awareness of both personal and social difficulties in achieving them put a strain on both patients and their families.Some studies conducted in the USA and in various European countries underline that the transition to adulthood of patients with muscular dystrophy is featured by a good ability to adapt to the more advanced stages of the disease in general; nevertheless, facing the worsening of health entails experiences of anxiety and depression.In this historical phase, clinical trials of gene therapy and gene modulating therapies are involving an increasing number of patients, mainly represented by children in the early phase of the disease. Hence, adolescents and young adults could develop feelings of exclusion from research efforts, losing confidence and hope in any future improvement of their condition, social participation and quality of life.This study could lead to identify strengths and weaknesses in social cognition and psychosocial adaptation; through the evaluation of characteristics of patients/caregivers or exogenous factors influencing higher levels of social adaptation, we ultimately aim to define strategies to improve not only physical (already defined by guidelines) but also psychological care, social cognition and social support in all stages of DMD, particularly in later ones.

Participants needed: 250
Trial details
Age: 14+Biological sex: MaleType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Aug 3, 2025Locations: 1
Eligibility criteria

Defined diagnosis of DMD [+3]

Clinical history of cerebral palsy, severe intellectual deficit, severe behavior... [+1]

Status: Recruiting

Electroencephalogram in Patients With Friedreich's Ataxia for the Study of the Structural and Functional Connectome.

Prospective, exploratory, multicenter pilot study investigating the structural and functional connectome in patients with Friedreich's Ataxia (FRDA) using high-density electroencephalogram (HD-EEG). The aim is to identify neurophysiological biomarkers and analyze the relationship between cortical connectivity, cognitive functioning, and clinical severity, particularly in response to rehabilitation treatment.

Participants needed: 30
Trial details
Age: 8-60Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Jul 31, 2025Locations: 1
Eligibility criteria

age between 8 and 60 years; [+3]

age different from the range 8-60 years; [+3]

Status: Recruiting

Personalization of Visual Characters and Text-to-Speech (TTS) to Support Learning in Students With Reading Difficulties

Previous research has shown the importance of font type, size and spacing to facilitate text reading in dyslexia. A special automatized procedure was designed to select the most favorable parameters for both text visualization and text-to-speech (TTS) conversion to be used by students with reading difficulties. The validation of its outcomes will be carried out through a systematic comparison of the use of the personalized versus standard fonts and voices in reading and writing tests.

Participants needed: 90
Trial details
Age: 7-15Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: May 4, 2025Locations: 3
Eligibility criteria

age 7-15 years [+2]

special educational needs or diagnosis of neurodevelopmental disorders [+8]

Status: Recruiting

Dynamic Assessment of the Risk for Language and Reading Disorders in Monolingual and Multilingual Children

The project represents the completion of a part of the recently concluded European project MultiMind, in which a computer platform called MuLiMi was developed and validated. The platform hosts screening tests for the identification of the risk of Language and Learning Disorders in preschool and primary school children, respectively. The aim is to validate the Dynamic Assessment (DA) tests (a first test assessing the capacity to learn new words for preschool children and a second one assessing the capacity to learn a new spelling code for school-age children) in a population of monolingual and bilingual children attending preschool and primary school. The main goal of the study is to complete the validation of the two Dynamic Assessment tests implemented in the MuLiMi platform developed for the MultiMind project.

Participants needed: 150
Trial details
Age: 4-9Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: May 4, 2025Locations: 1
Eligibility criteria

age 4-6 years (Kindergarten) or 7-9 years (Primary school); [+3]

Intellectual disability, major psychopathological disorders, exposure to Italian...

Status: Recruiting

Robot-assisted Walking Treatment in Hereditary Spastic Paraplegia (HSP)

Patients will undergo a combined rehabilitation treatment consisting of 15 sessions on Lokomat and 15 sessions of physical therapy over three weeks for a total of 30 sessions. Two sessions/day for 5 days a week. The same subjects will conduct clinical-functional assessments before, at the end of treatment, and after a 3-month follow-up: 3D Gait Analysis with defined protocol (BTSBioenginner); Spastic Paraplegia Rating Scale (SPRS); Six-Minute Walk Test (6MWT), Ten Meters Walk Test (10MWT), Gross Motor Function Measure-88 (GMFM-88) and Berg Balance Scale (BBS); Quality of life questionnaires: Medical Outcome Survey Short Form (SF-36) and ad hoc questionnaire for subjective assessment of symptoms during walking (HSP-SNAP). This study is part of normal clinical practice and does not involve any changes to the current rehabilitation course for patients.

Participants needed: 50
Trial details
Age: 4-70Biological sex: AllType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: May 4, 2025Locations: 1
Eligibility criteria

genetic or clinical diagnosis of HSP. [+3]

botulinum toxin injection or lower limb surgery in the previous 6 months [+6]

Status: Recruiting

Cp eArly REhabilitation

The present study aims to investigate the efficacy of play-based rehabilitation delivered as usual care in children with cerebral palsy in a rehabilitation center offering both intensive and extensive care. Up to now, few studies described and examined treatments' efficacy in this population. Secondary aim of the study will be comparing the efficacy of the two rehabilitation treatment formats (intensive vs. extensive), which will have the same dose (sessions delivered) and ingredients (content). The intervention delivered as extensive care (3 sessions per week per 15 weeks) will be offered in community rehabilitation centers (Centri di Riabilitazione-CDR), while the one delivered as intensive care (3 sessions daily per 5 days a week for 3 weeks) will be offered to children admitted to hospital inpatient care units. This comparison allows verifying if delivery time may affect outcomes.

Participants needed: 96
Trial details
Age: 36-5Biological sex: AllType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: May 1, 2025Locations: 6
Eligibility criteria

age between 6 months (corrected age in case of prematurity) and 5 years; [+1]

profound deafness and/or severe hypovisus/blindness; [+1]

Status: Recruiting

Efficacy of Stabilometric Platform to Improve Standing Balance in Patients With Friedreich's Ataxia

The primary objective is to evaluate the potential effectiveness of an individualized intensive rehabilitation intervention using the "Prokin 252" stabilometric platform in the treatment of adolescent and adult patients with Friedreich's Ataxia. The secondary objective is to assess the retention of the rehabilitation treatment effects over time. Enrolled patients will be randomized and assigned to one of two treatment groups for four weeks. Three assessments will be conducted for each patient: one before treatment (T0), one at the end of treatment (T1), and a follow-up assessment 90 days after T1 via telemedicine (T2). This study is: * Exploratory: The study aims to explore the usefulness of the stabilometric platform in a rehabilitative setting in combination with conventional therapy; * Not "first-in-human"; * Longitudinal: The study will investigate changes over time in motor and functional ability scales, as well as stabilometric platform parameters, within the same cohort; * Randomized, controlled, open-label; * Monocentric: The study will be conducted only at the "La Nostra Famiglia" Association in Conegliano and Pieve di Soligo - IRCCS Eugenio Medea in Conegliano - UOC Neuromotor Rehabilitation in Pieve di Soligo, Via Monte Grappa, 96, 31053 Pieve di Soligo TV; * Prospective; * Post-market.

Participants needed: 24
Trial details
Age: 14+Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: May 2, 2025Locations: 1
Eligibility criteria

Age ≥ 14 years; [+3]

Age < 14 years; [+7]

Status: Recruiting

Sustained Endogenous Attention Deficits in Attention Deficit Hyperactivity Disorder

Subjects with ADHD may exhibit deficits in sustained internal attention. The "Sustained-Paced Finger Tapping" test was recently developed and experimentally used in international literature to assess sustained internal attention in typically developing children. This clinical study has several objectives: 1) to assess the presence of "internal" sustained attention deficits in children with ADHD through the "Sustained-Paced Finger Tapping"; 2) to evaluate the discriminant and ecological validity of the "Sustained-Paced Finger Tapping."

Participants needed: 50
Trial details
Age: 6-13Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Mar 28, 2025Locations: 2
Eligibility criteria

ADHD Group (1) Subjects with a diagnosis of ADHD of any severity level and subty... [+3]

for both groups, symptomatology suggestive of autism spectrum disorders, psychot... [+4]

Status: Not yet recruiting

Social Cognition in Dystrophinopathies and Neurodevelopmental Disorders

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.

Participants needed: 45
Trial details
Age: 4+Biological sex: MaleType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: Mar 13, 2025
Eligibility criteria

Patients diagnosed with Duchenne and Becker muscular dystrophy (genetic and hist... [+2]

presence of comorbid diagnoses, [+3]

Status: Recruiting

Assessment of Navigation Abilities in Children With Cerebral Palsy and Their Peers

Spatial navigation skills are very important in everyday activities and quality of life but spatial navigation abilities are not part of the standard process of assessment and rehabilitation of patients. Furthermore, it is known that children with cerebral palsy have impaired visuo-spatial competences. The main objective of this study is to evaluate and compare the spatial navigation abilities of typically developing children and of children with cerebral palsy using the "StarMaze" application delivered by means of a Head Mounted Display (HMD). The second aim is to investigate the user experience during the session. A similar application was already developed and tested in a virtual reality large scale platform whose size and cost limit the accessibility. Therefore, the assessment (and future training) of navigation abilities with affordable and easy-to-use technology such as HMD open new perspectives.

Participants needed: 26
Trial details
Age: 13+Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Feb 26, 2025Locations: 1
Eligibility criteria

IQ higher than 70

Subjects with epileptic issues [+2]

Status: Recruiting

Expanding NGS Data with Optical Genome Mapping (OGM)

Over 50% of pediatric neurological and neurodevelopmental disorders lack a molecular diagnosis after standard DNA sequencing and molecular karyotyping. This is due to technical limitations, incomplete variant interpretation, and inadequate genotype-phenotype correlations. New sequencing technologies are crucial for clinical decision-making, offering complete profiles of variants in a patient's DNA to personalize treatment. Optical Genome Mapping (OGM) can detect nearly all structural variants in one experiment. This project aims to use OGM alongside NGS to improve diagnostic yield in 60 children with severe disorders who tested negative for NGS/CMA.

Participants needed: 60
Trial details
Age: 2+Biological sex: AllType: InterventionalSponsor: IRCCS Eugenio MedeaUpdated: Feb 28, 2025Locations: 1
Eligibility criteria

individuals without a molecular diagnosis (negative to ES/CMA analyses); [+3]

individuals who have not undergone initial diagnostic genetic tests (ES/CMA)

Status: Recruiting

Intensive Physiotherapy in Children Affected by Posterior Fossa Tumors

The objective of the current study is to describe the effectiveness of conventional and intensive physiotherapeutic intervention in improving gross motor skills (i.e. postural changes, walking and balance skills) in children affected by posterior fossa tumors

Participants needed: 40
Trial details
Age: 0-25Biological sex: AllType: ObservationalSponsor: IRCCS Eugenio MedeaUpdated: Feb 18, 2025Locations: 3
Eligibility criteria

subjects who underwent to surgical resection of tumors located in posterior foss...

Subjects that are currently addressed to rehabilitative protocols availing of te...