RECRUITING

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

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Conditions

Cerebral PalsyInfant

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2023-03-26
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05781438

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:5 Months to 2 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Infants with or at high risk of cerebral palsy (CP) who either:
  2. * have been diagnosed with CP by a medical professional, or
  3. * are at high risk of CP defined as having both:
  4. * clinical brain imaging indicating CP, such as (i) white matter injury (cystic periventricular leukomalacia or periventricular hemorrhagic infarctions), (ii) hypoxic-ischemic encephalopathy, or (iii) neonatal stroke, and
  5. * a score less than 63 or more than 5 asymmetries on the Hammersmith Infant Neurological Examination (HINE).
  1. * prenatal substance abuse,
  2. * congenital malformations,
  3. * drug-resistant epilepsy,
  4. * visual impairment that hinders the infant from seeing toys,
  5. * hearing impairment that hinders the infant from responding to sound,
  6. * living in a location inaccessible by study personnel for in-home data collections,
  7. * participant over 50 lbs in weight.

Contacts and Locations

Study Contact

Barbara Sargent, PhD, PT
CONTACT
323-442-4823
bsargent@pt.usc.edu
Stacey C Dusing, PhD, PT
CONTACT
323-442-1022
stacey.dusing@pt.usc.edu

Principal Investigator

Barbara Sargent, PhD, PT
PRINCIPAL_INVESTIGATOR
University of Southern California, Division of Biokinesiology and Physical Therapy

Study Locations (Sites)

University of Southern California
Los Angeles, California, 90089
United States

Collaborators and Investigators

Sponsor: University of Southern California

  • Barbara Sargent, PhD, PT, PRINCIPAL_INVESTIGATOR, University of Southern California, Division of Biokinesiology and Physical Therapy

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-03-26
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2023-03-26
Study Completion Date2024-12-31

Terms related to this study

Keywords Provided by Researchers

  • Infant

Additional Relevant MeSH Terms

  • Cerebral Palsy