Actively Recruiting

Phase Not Applicable
Age: 5Months - 2Years
All Genders
NCT05781438

Feasibility of an In-home Standing and Walking Intervention for Infants With and at High Risk of Cerebral Palsy

Led by University of Southern California · Updated on 2025-06-26

8

Participants Needed

1

Research Sites

196 weeks

Total Duration

On this page

Sponsors

U

University of Southern California

Lead Sponsor

C

California Physical Therapy Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to evaluate the feasibility and begin to evaluate the effect of an intensive in-home standing and walking intervention for infants with or at high risk of cerebral palsy.

CONDITIONS

Official Title

Feasibility of an In-home Standing and Walking Intervention for Infants With and at High Risk of Cerebral Palsy

Who Can Participate

Age: 5Months - 2Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Infants aged 5 to 12 months with or at high risk of cerebral palsy
  • Diagnosed with cerebral palsy by a medical professional, or considered high risk defined by clinical brain imaging indicating CP
  • High risk also requires a Hammersmith Infant Neurological Examination (HINE) score less than 63 or more than 5 asymmetries
Not Eligible

You will not qualify if you...

  • Prenatal substance abuse
  • Congenital malformations
  • Drug-resistant epilepsy
  • Visual impairment preventing the infant from seeing toys
  • Hearing impairment preventing the infant from responding to sound
  • Living in a location inaccessible to study personnel for in-home visits
  • Participant weighing over 50 pounds

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Southern California

Los Angeles, California, United States, 90089

Actively Recruiting

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Research Team

B

Barbara Sargent, PhD, PT

CONTACT

S

Stacey C Dusing, PhD, PT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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