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Study identifier: NCT07493096 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Intensive Multimodal Neurorehabilitation Targeting Neuroplasticity in Pediatric Neurodevelopmental and Chromosomal Disorders

Condition: Neurodevelopmental Disorders · Neurodevelopmental Disorders (NDD) · Neurodevelopmental Disorders and Developmental Abnormalities  ·  Sponsor: Healing Hope International

PhaseN/A
Planned participants100
Who can joinAll sexes, 4 Years to 12 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Genelle Mills, OTR/L  ·  (480) 620-4514  ·  genelle@abilityandbeyond.com

Tamara Tamas, MS RA  ·  (863) 354- 5131

Always discuss trial participation with your own doctor first.

Locations (1)

Ability and BeyondThe Woodlands, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07493096