CHAMP Project (Child Hand Arm Movement Project)

  • STATUS
    Recruiting
  • sponsor
    NICHD
Updated on 8 November 2020

Summary

CHAMP Project (Child Hand Arm Movement Project)

Description

The CHAMP Study—a multisite clinical trial funded by the National Institutes of Health—compares the efficacy of alternative therapies for young children with unilateral spastic cerebral palsy, also known as hemiparetic cerebral palsy.

Children who meet study eligibility criteria will participate at one of the three clinical sites— Roanoke, Virginia; Charlottesville, Virginia; and Columbus, Ohio. After enrollment children will be randomly assigned to one of the 5 alternative therapy. All of which will receive an intensive rehabilitation treatment designed to promote functional skills of the child's weaker arm and hand. Participation in the study includes assessment of each child prior to treatment, close monitoring of the child’s progress during treatment, and post-treatment evaluation at the end of therapy, as well as at 6 and 12 months later.

There is no cost associated with therapy services, but families who live outside of the treatment cities will be responsible for travel related expenses associated with assessments and the 4-week treatment period.

Details
Condition Cerebral Palsy (Pediatric)
Clinical Study IdentifierTX146126
SponsorNICHD
Last Modified on8 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

Your child may be eligible to participate in the study if he or she
Has a neuromotor impairment that mostly affects one side of the body
Is between two and eight years old (up to the ninth birthday)
Has cerebral palsy or an acquired brain injury prior to the age of two; and
Is able to participate in four weeks of therapy
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note