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HemiparesisPhase 1/2The Baby CHAMPNCT02346825

The Baby CHAMP Study (Children With Hemiparesis Arm and Movement Project)

A Phase 1/2 study testing Neurorehabilitation therapy with cast, Neurorehabilitation therapy with splint and Neurorehabilitation bimanual in people with Hemiparesis and Cerebral Palsy, run by Virginia Polytechnic Institute and State University at 3 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The Baby CHAMP Study is a multisite clinical trial funded by the National Institutes of Health that is examining the the use of constraint-induced movement therapy (CIMT) for infants and toddlers as a effective treatment, since there have been no randomized control trials (RCT) for the age range as well as monitor the… Read more about this study

Who is it for?
Ages 6 to 24 months
Conditions the study is for
Hemiparesis, Cerebral Palsy
What is being tested?
Neurorehabilitation therapy with cast, Neurorehabilitation therapy with splint and Neurorehabilitation bimanual
Could I receive a placebo?
No, everyone receives an active treatment
How many people
58 participants
Where
3 sitesUnited States
Study dates
Jan 2015to Dec 2019
Phase
Phase 1/2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 24 months
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • child is 6 - 24 months old
  • diagnosis of unilateral/asymmetrical Cerebral Palsy
  • has functional upper extremity impairment levels of II, III, or IV (Manual Abilities Classification System, Eliasson et al 2006)
  • parent(s) willing to be partners in study and participate in follow-up assessments for 12 mos.

Who cannot join

  • medical or sensory condition that prevents full therapy participation (e.g., frequent uncontrolled seizures, blindness)
  • received CIMT or had botulinum toxin therapy in past 6 mos.

Trial locations and contacts

3 sites in 1 country.

United States3 sites
  • University of Virginia

    Charlottesville, Virginia

  • The Ohio State University

    Columbus, Ohio

  • Fralin Biomedical Research Institute at Virginia Tech

    Roanoke, Virginia, 24016

Other trials in United States

About this study

Official title: Multisite RCT of 3 Neurorehabilitation Therapies for Infants With Asymmetrical Cerebral Palsy

The Baby CHAMP Study is a multisite clinical trial funded by the National Institutes of Health that is examining the the use of constraint-induced movement therapy (CIMT) for infants and toddlers as a effective treatment, since there have been no randomized control trials (RCT) for the age range as well as monitor the stress levels as related by self-report of parents or biological indicators. Infants and toddlers who meet study eligibility requirements at one of the three clinical sites (Charlottesville, VA, Columbus, OH, and Roanoke, VA) will be invited to enroll, and their parents will be provided all necessary paperwork along with informational documentation.

Read the detailed description

In 2013, a systematic review of interventions for children with cerebral palsy (Novak et al, 2013) concluded that constraint-induced movement therapy (CIMT) produces the largest magnitude effects of any non-surgical treatment. Similarly, the first major handbook summarizing the results from more than 50 studies on CIMT conducted worldwide (Ramey, Coker-Bolt, \& DeLuca, 2013) provides additional clinical and scientific support for the conclusion that CIMT can produce significant benefits. There are a number of important unresolved issues. One concerns the need for empirical evidence that CIMT is efficacious for infants and toddlers, since there has been no randomized controlled trial (RCT) focused on this age range. Another issue under debate is whether there are different effects related to the type of constraint used during the therapy. The constraint is placed on the child's "stronger" or non-hemiparetic upper extremity while the therapy focuses on improving the child's skills in using the impaired or hemiparetic upper extremity. Two widely used forms of constraint are: 1) a full-arm cast that the child wears continuously throughout a multi-week period when the child receives daily therapy and 2) a part-arm splint that the child wears only during the time of day when he or she receives therapy. Finally, another important topic that has not been studied is whether CIMT is a stressful form of therapy, because it is high-intensity (i.e., much higher dosage than the usual and customary sessions in other forms of occupational and physical therapy), involves constraining the child's non-involved or less involved upper extremity, and takes place in the child's home and often asks parents to help with practice sessions during non-therapy hours. If CIMT does produce elevated stress for the child, the parents, or both, is this stress short-term (i.e., just at the start of therapy) or does this continues over the entire period of therapy? Further, does the type of constraint used produce different levels of stress, either at first or throughout the course of therapy?

The proposed study is a randomized controlled trial (RCT) of CIMT for 72 children with hemiparetic spastic cerebral palsy (CP) between the ages of 6 and 24 months. The study will take place in two sites (Roanoke, VA and Columbus, OH), each site enrolling 36 children over a 3 year period. The study will address two specific aims:

Aim 1: to test the efficacy of 3 different constraint conditions used as part of administering a standardized form of therapy known as ACQUIRE (DeLuca, Echols, \& Ramey, 2007). The 3 constraint conditions are: i) continuous constraint, ii) part-time constraint, and iii) no constraint. In all 3 groups, children will receive 3 hours of therapy per day for 5 days per week for 4 consecutive days. Therapy is delivered by licensed occupation or physical therapists who have been trained to deliver ACQUIRE therapy to high fidelity. In addition, parents are trained to provide one hour of practice in their homes, using techniques compatible with those used by the ACQUIRE therapist. Efficacy will be measured primarily by changes in the children's assessed skill levels in using their upper extremities, both the hemiparetic (affected) and the non-hemiparetic (less involved) upper extremities, used alone and together (i.e., in completing bimanual tasks). In addition, changes in brain functioning related to receiving the 3 different constraint conditions will be measured using functional Near-Infrared Spectroscopy (fNIRS), a non-invasive and safe procedure that permits children to be active while recording takes place.

Aim 2: to monitor stress levels and safety risks related to use of constraint in the 3 conditions identified above (Aim 1). The study addresses stress levels in both the children and their parents, because CIMT is a high-intensity and unusual (i.e., constraining the child's "stronger arm") form of therapy taking place in the children's homes. Prior published clinical case reports indicate infants and toddlers adjust well to this form of therapy, and parents have favorable responses, no study previously has directly measured stress effects, related to self-report of parents or biological indicators, such as revealed by collecting saliva and hair samples to analyze for cortisol levels and changes over time.

The study results are expected to be important to inform the field of infant rehabilitation and provide much-needed evidence about whether infants and toddlers show significant (clinically meaningful) benefits from one or more of the 3 forms of therapy being tested. The findings will include evidence about both behavioral and brain changes. Further, the evidence will answer questions about whether the immediate therapy benefits, if detected, continue to be measurable at 6 and 12 months after therapy has ended. In addition, the study will yield first-ever evidence about whether CIMT is stressful for children and their parents. It may be there are some children or parents who are at higher risk for showing stress effects. If so, the data generated by this study will be important for future clinical practice and research to reduce these levels. If elevated stress does not occur, or if markedly lowering of stress is detected, then these findings will help to resolve the uncertainty that currently prevents some families or clinicians from considering this form of therapy, despite the fact that other scientific studies have shown it produces large and lasting benefits for children age 2 and older.

Being tested
Neurorehabilitation therapy with cast, Neurorehabilitation therapy with splint, Neurorehabilitation bimanual
Keywords
P-CIMT, Pediatric Constraint Induced Movement Therapy, Hemiparesis, Cerebral Palsy, Infants, Toddlers, Children
Medical subject headings
Paresis, Cerebral Palsy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Neurorehabilitation therapy with castBehavioural

    Also called Pediatric Constraint-Induced Movement Therapy, P-CIMT

    Children in this group will have 3 hours of daily therapy each weekday for 4 weeks while wearing a full-arm cast on their stronger arm and hand. Parents will be required to do 45 minutes of daily therapy for which they will be trained.

  • Neurorehabilitation therapy with splintBehavioural

    Also called Pediatric Constraint-Induced Movement Therapy, P-CIMT

    Children in this group will have 3 hours of daily therapy each weekday for 4 weeks while wearing part-time splint on their stronger arm and hand. Parents will be required to do 45 minutes of daily therapy for which they will be trained.

  • Neurorehabilitation bimanualBehavioural

    Also called Bimanual, HABIT

    Children in this group will have 3 hours of daily therapy each weekday for 4 weeks will not wear a constraint. Parents will be required to do 45 minutes of daily therapy for which they will be trained.

Study groups in NCT02346825
Study groupRoleWhat they receive
Intensive Plus CastExperimentalChildren in this group will have 3 hours of daily therapy each weekday for 4 weeks while wearing a full-arm cast on their stronger arm and hand. Parents will be required to do 45 minutes of daily therapy for which they will be trained.
Receives: Behavioral: Neurorehabilitation therapy with cast
Intensive Plus SplintExperimentalChildren in this group will have 3 hours of daily therapy each weekday for 4 weeks while wearing a part-time splint on their stronger arm and hand. Parents will be required to do 45 minutes of daily therapy for which they will be trained.
Receives: Behavioral: Neurorehabilitation therapy with splint
Intensive no ConstraintExperimentalChildren in this group will have 3 hours of daily therapy each weekday for 4 weeks but will not wear a constraint. Parents will be required to do 45 minutes of daily therapy for which they will be trained.
Receives: Behavioral: Neurorehabilitation bimanual

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in the Mini - Assisting Hand Assessment

    functional assessment

    Measured: immediatly prior to treatment, immediately after treatment, 6 months after treatment, 12 months after treatment

  2. Change in the Bayley Infant Scales of Development

    functional assessment

    Measured: immediatly prior to treatment, immediately after treatment, 6 months after treatment, 12 months after treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Jan 2015 (estimated)
  2. Study startJan 2015
  3. Primary completionDec 2018
  4. Study completionDec 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1/2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Factorial
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
58 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02346825
Sponsor's protocol ID
1R01HD074574-01A1
Acronym
The Baby CHAMP
Status last verified
Mar 2022
First submitted
15 Jan 2015
Last updated
11 Mar 2022
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing Neurorehabilitation therapy with cast, Neurorehabilitation therapy with splint and Neurorehabilitation bimanual in people with Hemiparesis and Cerebral Palsy, run by Virginia Polytechnic Institute and State University at 3 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Mar 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in the Mini - Assisting Hand Assessment (time frame: immediatly prior to treatment, immediately after treatment, 6 months after treatment, 12 months after treatment). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Mar 2022.

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The Baby CHAMP Clinical Trial NCT02346825 | AzTrials