RECRUITING

School Readiness in Preschool-Aged Children With Cerebral Palsy

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 goal of this feasibility and proof of concept study is to learn about the feasibility, acceptability, and impact of a school readiness program for preschool-aged children with unilateral cerebral palsy. The main question\[s\] it aims to answer are: 1. Is it feasible to implement an intensive school readiness program for preschool-aged children with UCP? 2. Is the program acceptable to the children and their caregivers? 3. What is the impact of the program on school readiness? Participants will complete two pre-intervention assessments, participate in an intensive, goal directed, school readiness program, and complete 1 post-intervention assessment.

Official Title

School Readiness in Preschool-Aged Children With Cerebral Palsy

Quick Facts

Study Start:2023-12-12
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06083220

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:36 Months to 71 Months
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * ages 3 years to 5 years 11 months
  2. * unilateral cerebral palsy
  3. * ability to visually attend to objects
  4. * demonstrates an interest in objects
  5. * attempt to reach for or grasp an item with the impaired upper extremity
  6. * English-speaking participants
  1. * uncontrolled epilepsy
  2. * significant visual impairment
  3. * severe behavioral problems
  4. * inability to complete the assessment protocol

Contacts and Locations

Study Contact

Angela Shierk, PhD
CONTACT
(469) 412-7172
angela.shierk@tsrh.org

Principal Investigator

Angela Shierk, PhD
PRINCIPAL_INVESTIGATOR
Scottish Rite for Children

Study Locations (Sites)

Scottish Rite for Children
Frisco, Texas, 75034
United States

Collaborators and Investigators

Sponsor: Texas Scottish Rite Hospital for Children

  • Angela Shierk, PhD, PRINCIPAL_INVESTIGATOR, Scottish Rite for Children

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 Date2023-12-12
Study Completion Date2025-12

Study Record Updates

Study Start Date2023-12-12
Study Completion Date2025-12

Terms related to this study

Additional Relevant MeSH Terms

  • Unilateral Cerebral Palsy
  • School Readiness