← Back to Search

Behavioral Intervention

CP intervention group for Cerebral Palsy

N/A
Waitlist Available
Led By Citlali Lopez-Ortiz
Research Sponsored by University of Illinois at Urbana-Champaign
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up tested during the assessment sessions and on the first and last day of gameplay spanning over a 6 to 7 week period.
Awards & highlights
No Placebo-Only Group

Summary

This game-like intervention using virtual reality will provide an objective and quantitative characterization of dystonia and spasticity presentations in cerebral palsy, even if combined, through the process of motor learning. This intervention could have a therapeutic benefit in the rehabilitation of children with cerebral palsy.

Eligible Conditions
  • Cerebral Palsy

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~tested during the assessment sessions and on the first and last day of gameplay spanning over a 6 to 7 week period.
This trial's timeline: 3 weeks for screening, Varies for treatment, and tested during the assessment sessions and on the first and last day of gameplay spanning over a 6 to 7 week period. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Smoothness Index
Secondary study objectives
Dyskinesia Impairment Scale (DIS)
Forces and torques against force sensor during gampeplay and in robotic zero-force channel
Montreal Spasticity Rating Test (MSRT)
+6 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

4Treatment groups
Experimental Treatment
Active Control
Group I: TD intervention groupExperimental Treatment1 Intervention
Force efforts haptic feedback in virtual reality. The intervention will be the same as the CP intervention group but for typically developing participants.
Group II: CP intervention groupExperimental Treatment1 Intervention
Force efforts with haptic feedback in virtual reality for participants with CP.
Group III: CP control groupActive Control1 Intervention
Regular activity control group, for participants with CP.
Group IV: TD control groupActive Control1 Intervention
Regular activity control group, same as CP no intervention group, but for typically developing participants.

Find a Location

Who is running the clinical trial?

University of Illinois College of Medicine at PeoriaOTHER
14 Previous Clinical Trials
6,019 Total Patients Enrolled
University of Illinois at Urbana-ChampaignLead Sponsor
197 Previous Clinical Trials
38,207 Total Patients Enrolled
OSF Healthcare SystemOTHER
30 Previous Clinical Trials
33,688 Total Patients Enrolled
~10 spots leftby Nov 2025