NCT06102330 Multicenter HomeVENT: Home Values and Experiences Navigation Track
| NCT ID | NCT06102330 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Johns Hopkins University |
| Condition | Pediatric ALL |
| Study Type | INTERVENTIONAL |
| Enrollment | 600 participants |
| Start Date | 2024-02-06 |
| Primary Completion | 2029-12 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 600 participants in total. It began in 2024-02-06 with a primary completion date of 2029-12.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This is a multicenter study to test a decision-making support process for families and clinicians facing decisions about chronic home ventilation for a child. The investigators hypothesize that the intervention will increase family preparedness for decision-making and will improve clinician-family shared-decision making. Half of families will be assigned to "usual care" arm and half to the "intervention" arm. Intervention families will view the study website with study staff and will answer questions related to website content. All families will be interviewed and surveyed at 1, 6 and 12 months after enrollment. Each family will designate 1-2 physician involved in the decision about home ventilation; each physician will be interviewed and surveyed at 1 month.
Eligibility Criteria
Inclusion Criteria: 1. English- or Spanish-speaking 2. Males and females; Age 18 and over. 3. Parent of a child facing a decision about home ventilation within 30 days. A "parent" will be defined as any self-identified primary caregiver (parents, grandparents, etc). or Physician of a child whose parents are enrolled in the study; physician must be engaged in the home ventilation decision. 4. Provision of signed and dated informed consent form (parent) or completion of oral consent (physician) 5. Stated willingness to comply with all study procedures and availability for the duration of the study 6. Access to necessary resources if choose to participate via internet or telephone Exclusion Criteria: 1. Excluding children as they cannot be legal decision-makers 2. Non-English or Non-Spanish speaking parents, as the intervention website/ videos are only available in those two languages.
Contact & Investigator
Renee Boss, MD
PRINCIPAL INVESTIGATOR
Johns Hopkins School of Medicine
Frequently Asked Questions
Who can join the NCT06102330 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Pediatric ALL. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06102330 currently recruiting?
Yes, NCT06102330 is actively recruiting participants. Contact the research team at rboss1@jhu.edu for enrollment information.
Where is the NCT06102330 trial being conducted?
This trial is being conducted at Tampa, United States, New Orleans, United States, Baltimore, United States, Seattle, United States.
Who is sponsoring the NCT06102330 clinical trial?
NCT06102330 is sponsored by Johns Hopkins University. The principal investigator is Renee Boss, MD at Johns Hopkins School of Medicine. The trial plans to enroll 600 participants.