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Behavioral Intervention

Health Coaching via Text Messaging for Cerebral Palsy (RE-PACT Trial)

N/A
Waitlist Available
Led By Ryan Coller, MD, MPH
Research Sponsored by University of Wisconsin, Madison
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Has a child aged 0-17 years with Gross Motor Function Classification System level IV or V Cerebral Palsy, cared for by respiratory specialist or receive daily respiratory treatments (oxygen, ventilation, airway clearance device, medications)
Be at least 18 years of age
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 24 months
Awards & highlights

RE-PACT Trial Summary

This trial will test a new way to reduce respiratory illnesses in children with severe cerebral palsy, by using text messages to deliver timely, customized health coaching.

Who is the study for?
This trial is for primary caregivers of children aged 0-17 with severe cerebral palsy (GMFCS level IV or V), who are under respiratory specialist care or receive daily treatments. Caregivers must be adults, speak English or Spanish, and have a text-capable phone. Those not interested in text messaging or coaching are excluded.Check my eligibility
What is being tested?
The RE-PACT Intervention is being tested to see if it can reduce hospitalizations due to severe respiratory illness in children with severe CP by providing customized action plans and health coaching through mobile texts when the risk is high.See study design
What are the potential side effects?
Since RE-PACT involves non-medical interventions like action planning and health coaching via text messages, there are no direct medical side effects associated with this study.

RE-PACT Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My child with severe cerebral palsy receives daily respiratory care.
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I am 18 years old or older.
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I can communicate well in English or Spanish.

RE-PACT Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 24 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 24 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Acceptability: Categorized Reasons for Consent Refusal
Acceptability: Participant Drop Out Rate
Acceptability: Participant Enrollment Rate
+15 more
Secondary outcome measures
Child Mortality Rate
Incidence of Respiratory Diagnosis Requiring Hospitalization
Number of Respiratory Emergency Department Visits
+3 more
Other outcome measures
Caregiver General Self-Efficacy Scale (GSES) - mean composite score
Confidence Responses mHealth texting (weekly score 1 through 10)
Family Caregiver Activation in Transition Measure (FCAT) - mean composite score
+1 more

RE-PACT Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: RE-PACT InterventionExperimental Treatment1 Intervention
Intervention participants receive respiratory illness action plans and weekly mobile health (mHealth) confidence surveillance. At times of low confidence or hospitalization, just-in-time action planning and coaching activities are conducted.
Group II: Active Control (AC)Active Control1 Intervention
AC subjects will receive usual comprehensive medical care and coordination.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
RE-PACT Intervention
2022
N/A
~60

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Cerebral Palsy (CP) include physical and occupational therapy, pharmacologic interventions, and surgical options. Physical and occupational therapy aim to improve motor function and daily living skills through targeted exercises and activities. Pharmacologic treatments, such as muscle relaxants and botulinum toxin injections, help manage spasticity and dystonia by reducing muscle tone and preventing muscle contractures. Surgical interventions, like selective dorsal rhizotomy, address severe spasticity by cutting nerve roots to reduce muscle stiffness. The RE-PACT trial's just-in-time adaptive intervention, which uses mobile text messaging for timely action planning and health coaching, highlights the importance of personalized and proactive care in managing CP. This approach can help mitigate hospitalization risks by addressing health issues promptly and tailoring interventions to individual needs, thereby improving overall quality of life for CP patients.

Find a Location

Who is running the clinical trial?

University of Wisconsin, MadisonLead Sponsor
1,193 Previous Clinical Trials
3,161,779 Total Patients Enrolled
1 Trials studying Cerebral Palsy
10 Patients Enrolled for Cerebral Palsy
National Heart, Lung, and Blood Institute (NHLBI)NIH
3,847 Previous Clinical Trials
47,818,176 Total Patients Enrolled
Ryan Coller, MD, MPHPrincipal InvestigatorUW School of Medicine and Public Health
3 Previous Clinical Trials
426 Total Patients Enrolled

Media Library

RE-PACT Intervention (Behavioral Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05292365 — N/A
Cerebral Palsy Research Study Groups: RE-PACT Intervention, Active Control (AC)
Cerebral Palsy Clinical Trial 2023: RE-PACT Intervention Highlights & Side Effects. Trial Name: NCT05292365 — N/A
RE-PACT Intervention (Behavioral Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05292365 — N/A
~19 spots leftby Jun 2025