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Supervised Fitness Program for Adults With Cerebral Palsy

Virginia Commonwealth University (VCU) logo

Virginia Commonwealth University (VCU)

Status

Completed

Conditions

Cerebral Palsy

Treatments

Behavioral: Home Exercise Group
Behavioral: Fitness Center Group

Study type

Interventional

Funder types

Other

Identifiers

NCT03218774
HM20009344

Details and patient eligibility

About

The purpose of this study is to compare the effectiveness of 2 community intervention approaches to maintain community mobility and walking speed in adults with cerebral palsy who have previously completed an 8 week course of physical therapy.

Full description

The proposed study will address the lifelong need for fitness in adults with cerebral palsy compared to individuals provided with a home exercise program at the end of their individualized physical therapy, individuals in the fitness group will...

Primary Hypothesis:

  1. Have higher Pediatric Evaluation of Disability Inventory Computer Adapted Test (PEDICAT) scores at the +12 weeks post intervention visit

  2. Increase their PEDICAT scores across the study period, while the home fitness group will decrease performance on the PEDICAT.

  3. Complete the Timed Up and Go (TUG) more quickly at +12 weeks post intervention

    Secondary Hypothesis (study not powered for these variables):

  4. Walk further on the Six Minute Walk Test (6MWT) at the +12 weeks post intervention visit

Enrollment

18 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults with cerebral palsy Gross Motor Function Classification System (GMFCS) level I, II, or III
  • Completion of episode of physical therapy provided by the Developmental Disabilities program at Sheltering Arms within the one month prior to the baseline assessment
  • Lives within the community in their own home or group housing

Exclusion criteria

  • GMFCS level IV or V
  • Unable to follow two-step directions
  • Adults who have a medical or legal power of attorney who sign their health authorization

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

18 participants in 2 patient groups

Home Group
Other group
Treatment:
Behavioral: Home Exercise Group
Center Group
Experimental group
Treatment:
Behavioral: Fitness Center Group

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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