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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
No Placebo-Only Group
Summary
This trial tests a program called RE-PACT that sends personalized health advice via text messages to families of children with severe cerebral palsy. It aims to reduce hospital visits by providing timely support when the child's health is at risk. The study involves 90 caregivers and will last for several months.
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.
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.
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.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My child with severe cerebral palsy receives daily respiratory care.
Select...
I am 18 years old or older.
Select...
I can communicate well in English or Spanish.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 24 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Acceptability: Categorized Reasons for Consent Refusal
Acceptability: Participant Drop Out Rate
Acceptability: Participant Enrollment Rate
+15 moreSecondary study objectives
Incidence of Respiratory Diagnosis Requiring Hospitalization
Other study objectives
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 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
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
1,226 Previous Clinical Trials
3,168,614 Total Patients Enrolled
2 Trials studying Cerebral Palsy
110 Patients Enrolled for Cerebral Palsy
National Heart, Lung, and Blood Institute (NHLBI)NIH
3,922 Previous Clinical Trials
47,760,686 Total Patients Enrolled
Ryan Coller, MD, MPHPrincipal InvestigatorUW School of Medicine and Public Health
3 Previous Clinical Trials
467 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My child with severe cerebral palsy receives daily respiratory care.I am 18 years old or older.I am not interested in text messaging or coaching during the study.I can communicate well in English or Spanish.
Research Study Groups:
This trial has the following groups:- Group 1: RE-PACT Intervention
- Group 2: Active Control (AC)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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