NCT07493096Recruiting
Intensive Multimodal Neurorehabilitation Targeting Neuroplasticity in Pediatric Neurodevelopmental and Chromosomal Disorders
Functional and Neurodevelopmental Outcomes Following Intensive Multimodal Neurorehabilitation in Pediatric Patients With Neurodevelopmental Disorders, Including Chromosomal Abnormalities
Source: ClinicalTrials.gov · Last updated 25 Mar 2026
Brief summary (registry, in English)
This observational study evaluates functional and developmental outcomes in pediatric participants undergoing a two week intensive multimodal neurorehabilitation program. The program is designed for children with neurodevelopmental disorders, including but not limited to cerebral palsy, autism spectrum disorder, developmental delay, hypoxic ischemic encephalopathy (HIE), and chromosomal or genetic abnormalities. Participants receive individualized therapy sessions for approximately 2.5 hours per day over a two week period. The intervention is not standardized but is tailored to each child's specific needs and may include components such as sensory integration, motor planning, reflex integration, oculomotor training, executive functioning activities, communication support, and other brain based therapeutic approaches. The purpose of this study is to observe changes in functional abilities, including attention, motor coordination, emotional regulation, communication, and activities of daily living. Outcomes are assessed using clinician observation and parent reported changes before and after the intensive program, with limited follow-up when available. This study does not assign participants to a specific treatment as part of a research protocol. Instead, it collects real world data from children already participating in a clinical therapy program to better understand potential benefits of intensive, individualized neurorehabilitation approaches.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 100 (estimated)
- First submitted
- 19 Mar 2026
- Start date
- 1 Mar 2026
- Primary completion date
- 1 Jan 2028
- Lead sponsor
- Healing Hope International
- Diseases
- Autism
- NCT number
- NCT07493096
What you commit to
- Study type: Observational
- Planned participants: 100
- From 1 Mar 2026 to the primary completion date, 1 Jan 2028
- 1 site in 1 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.
Prior treatment
- Concurrent participation in another structured intervention or clinical study that would confound interpretation of functional outcomes, at the discretion of the investigator.
Other illness
- Medical instability or acute medical condition that would prevent safe participation in an intensive therapy program.
- Severe uncontrolled seizure activity or other neurologic condition that would interfere with participation in structured therapeutic activities, as determined by the treating clinician.
- Behavioral or psychological conditions that would prevent safe engagement in the therapy environment despite appropriate support.
Other
- Inability to attend or complete the full two-week intensive program.
- Lack of sufficient baseline or post-intervention data to assess change in functional performance.
Who the study is looking for
- Pediatric participants between approximately 4 and 12 years of age at the time of enrollment.
- Diagnosed with or presenting with neurodevelopmental, neurologic, or genetic conditions, including but not limited to:
- cerebral palsy
- autism spectrum disorder
- developmental delay
- hypoxic ischemic encephalopathy (HIE)
- traumatic brain injury
- sensory processing disorder
- chromosomal or genetic abnormalities
- Demonstrate functional impairments in one or more neurodevelopmental domains, including:
- motor coordination or motor planning
- sensory processing
- attention or executive functioning
- oculomotor or visual processing
- communication
- emotional or behavioral regulation
- activities of daily living
- Enrolled in and able to participate in a two-week intensive therapy program consisting of approximately 2.5 hours per day/ 5 days per week
- Able to complete baseline and post-program clinical assessment using clinician-observed or caregiver-reported measures.
- Parent or legal guardian able to provide informed consent and participate in reporting functional outcomes when applicable.
Age in the registry: 4 years to 12 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Ability and Beyond Coordinator of this site? Confirm its status | The Woodlands | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.