Cerebral Palsy Adult Transition Longitudinal Study (CPAT)

University of Colorado Denver (CU Denver)

Status: Active, not recruiting

Conditions: Cerebral Palsy

Study type: Observational

Funder types: Other

Identifiers

NCT02137005

14-0367

H133G130200 (Other Grant/Funding Number)

Details and patient eligibility

About

The purpose of this study is to investigate longitudinally, the walking ability of individuals with cerebral palsy who are transitioning into adulthood and to cross-sectionally examine the health status of these individuals in the context of their walking ability. Young adults who received instrumented gait analysis (IGA) as children will show significant decreases in overall gait performance, as measured by kinematics, kinetics, temporal-spatial parameters, and gait deviation index, compared to their last childhood IGA.

Full description

The investigators are proposing a prospective, longitudinal, cross-sectional, and patient-centered outcome study of walking ability and current health status to investigate important health outcomes that impact the quality of life, participation, and activity on adults with cerebral palsy who took part in a gait analysis during childhood at the Center for Gait and Movement Analysis (CGMA). The goal is to see whether their health and walking ability has changed since leaving the Children's Hospital Colorado (CHCO) system and understand if there is a relationship between maintaining proper walking ability and health status. The investigators are including the measure of health outcomes to better understand if a decline in walking ability relates to a decline in health status. The first aim is to study the walking ability of adults with cerebral palsy by comparing their results of a gait analysis to the same results collected when they were children. The second aim is to study the presence of heart disease risk factors by testing each participant's blood levels of lipids, glucose, and insulin. The investigators will also measure each participant's blood pressure. The third aim is to study the relationship(s) between inflammatory markers, neurotrophic factors, and pain and fatigue levels. The investigators will measure inflammatory markers through a blood test and pain and fatigue levels through standardized assessments. The fourth aim is to study each participant's mental health. The investigators will measure this through standardized psychological assessments. The fifth aim is to study each participant's self-perceived health and quality of life as well as employment status. The investigators will measure these levels also through standardized assessments.

Enrollment: 72 estimated patients

Sex: All

Ages: 18 to 45 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male and female adults (aged 18 years or older) with cerebral palsy (CP)
• Adults with CP who are part of the CGMA data registry
• Adults with CP who have previously participated in an IGA at the CGMA
• Adults with CP who are able to walk (with or without assistance) three times down a ~35 foot walkway at a comfortable and self-selected pace
• Adults with CP who are able to give informed consent, or have a legally authorized representative to give informed consent
• Adults with CP who are able to understand and communicate in English or Spanish (medical interpreters will be utilized for this study when needed)
• If medicated, adults with CP will need to be on a stable medication regimen for at least six months prior to study enrollment (including non-steroidal anti-inflammatory drugs (NSAIDs))
• Adults with CP who are able to devote sufficient time to participate in a health/physical exam, respond to questions asked during assessments, and participate in an IGA
• Adults with CP who have no recent history of seizure or blackout

Exclusion criteria

• Male and female children (aged 17 years or younger) with CP
• Adults with CP who have never participated in an IGA at the CGMA
• Adults with CP whose mobility is impaired to the point of being unable to move (even with assistance)
• Adults with CP who are taking any medication(s) that might interfere with the ability to move
• Adults with CP who are unable to devote sufficient time to participate in a health/physical exam, respond to questions asked during assessments, and participate in an IGA
• Adults with CP who have any medical issue impacting performance

Trial design

72 participants in 1 patient group

Cerebral Palsy

Description:

Patients with cerebral palsy who were seen at the Center for Gait and Movement Analysis (CGMA) at Children's Hospital Colorado as children.