A Decentralized Clinical Trial to Promote Evidence-Based Care for Underserved Patients With Neurofibromatosis 1

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this fully decentralized, randomized controlled trial is to compare the efficacy of two educational interventions for individuals with Neurofibromatosis 1 (NF1). The primary objective of the study is to determine which intervention leads to higher rates of evidenced-based health screenings for NF1 patients in primary care settings. Adults with NF1 and parents/guardians of children with NF1 from across the U.S. who do not go to a specialized NF clinic and who have an upcoming annual wellness visits (e.g. an annual physical, a well-child visit, etc.) scheduled with a primary care provider (PCP) are eligible to enroll in the study. To see if you might be eligible, fill out a prescreening survey here: https://redcap.link/mynfguide

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Currently lives in the United States (including Puerto Rico and other United States territories)

• Has a clinical diagnosis of neurofibromatosis 1

• Does not attend an NF clinic within the Children's Tumor Foundation NF Clinic Network

• Has an in-person, well-person visit with a primary care provider scheduled within 3 months of their consent

• Speaks English or Spanish

• Currently lives in the United States (including Puerto Rico and other United States territories)

• Cares for a child (age \<18 years) with a clinical diagnosis of neurofibromatosis 1

• Does not attend an NF clinic within the Children's Tumor Foundation NF Clinic Network

• Their child has an in-person, well-person visit with a primary care provider scheduled within 3 months of their consent

• Speaks English or Spanish

Locations
United States
Massachusetts
Massachusetts General Hospital
RECRUITING
Boston
Contact Information
Primary
Paulina Arias Hernandez, MSW
pahernandez@mgb.org
6177245321
Backup
Evan Koch, BA
eokoch@mgh.harvard.edu
6177249574
Time Frame
Start Date: 2024-12-03
Estimated Completion Date: 2026-08
Participants
Target number of participants: 294
Treatments
Experimental: Intervention Arm
Experimental: Enhanced Usual Care Arm
Sponsors
Leads: Massachusetts General Hospital
Collaborators: Patient-Centered Outcomes Research Institute

This content was sourced from clinicaltrials.gov