- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05205356
VIGOR: Virtual Genome Center for Infant Health
This study will provide rigorous evaluation of implementing a virtual genome center into community clinical settings without highly specialized resources, thereby offering generalizable insights as to how best to implement genomic medicine at scale and for other age groups. This intervention has great potential to address disparities in genomic medicine among low-income and underrepresented minority (URM) populations and will enhance capacity for providers and health systems to utilize highly specialized genomic techniques in their communities.
The goal of this study is to achieve equitable access to state-of-the-art genomic medical care to sick newborns in community centers that predominately care for low-income and racial/ethnic minority populations through the creation of a virtual genome center (VIGOR). VIGOR will provide a venue for physician and family education, genomic expert consultation, reanalysis of unsolved sequencing data, and access to cutting edge therapeutic innovation, thereby facilitating institutionalization of genomic best practices in community settings, and not just highly specialized referral centers.
Study Overview
Status
Detailed Description
Genomic medicine has rapidly advanced in the past decade enabling earlier diagnosis and personalized treatment. However, only a few highly specialized centers in the US have the resources to take advantage of these advances in patient care. This has created a large health equity gap whereby patients cared for in typical community settings, often low-income and/or representing racial/ethnic minorities, do not receive equitable medical care. Another barrier to the wider utilization of genomic medicine is the poor dissemination of knowledge among clinicians, especially in community settings. A wide gap exists in the implementation of genomic medicine from diagnosis to personalized therapies, a field experiencing huge advances but still subject to wide disparities in accessibility. This study aims to develop and test the implementation of a strategy to break down these barriers to genomic medicine. The target population is sick newborns admitted to the NICU that present with probable genetic conditions. This study proposes a novel center, VIrtual GenOme CenteR (VIGOR). VIGOR will be a center that can remotely support clinicians and families working in community NICUs.
This study will provide rigorous evaluation of implementing a virtual genome center at community clinical settings without highly specialized resources, thereby offering generalizable insights as to how best to implement genomic medicine at scale and for other age groups. This intervention has great potential to address disparities in genomic medicine among low-income and underrepresented minorities (URM) populations and will enhance capacity for providers and health systems to utilize highly specialized genomic techniques in their communities.
The goal of this study is to achieve equitable access to state-of-the-art genomic medical care to sick newborns in community centers that predominately care for low-income and racial/ethnic minority populations through the creation of a virtual genome center (VIGOR). VIGOR will provide a venue for physician and family education, genomic expert consultation, reanalysis of unsolved sequencing data, and access to cutting edge therapeutic innovation, thereby facilitating institutionalization of genomic best practices in community settings, and not just highly specialized referral centers.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Vanessa J Young, MS, BA, RN
- Phone Number: 617-355-8330
- Email: vanessa.young@childrens.harvard.edu
Study Contact Backup
- Name: Timothy Yu, MD, PhD
- Phone Number: 617-919-7499
- Email: timothy.yu@childrens.harvard.edu
Study Locations
-
-
Florida
-
Miami, Florida, United States, 33136
- Not yet recruiting
- Holtz Children's Hospital at Jackson Memorial Medical Center
-
Contact:
- Pankaj Agrawal, MD, MMSC
- Phone Number: 617-919-2357
- Email: pagrawal@miami.edu
-
Principal Investigator:
- Pankaj Agrawal, MD, MMSC
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02118
- Recruiting
- Boston Medical Center
-
Contact:
- Bharati Sinha, MD
- Email: Bharati.Sinha@bmc.org
-
Principal Investigator:
- Bharati Sinha, MD
-
Springfield, Massachusetts, United States, 01199
- Recruiting
- Baystate Medical Center
-
Contact:
- Robert Rothstein
- Phone Number: 413-794-2400
- Email: Robert.rothstein@baystatehealth.org
-
Principal Investigator:
- Robert Rothstein, MD
-
Worcester, Massachusetts, United States, 01605
- Recruiting
- UMass Memorial Hospital
-
Contact:
- Lawrence Rhein, MD, MPH
- Phone Number: 508-334-6206
- Email: lawrence.rhein@umassmemorial.org
-
Principal Investigator:
- Lawrence Rhein, MD, MPH
-
Contact:
- Anjana Bhami Shenoy
- Phone Number: 508-334-6090
- Email: anjanabhami.shenoy@umassmed.edu
-
-
New Jersey
-
Camden, New Jersey, United States, 08103
- Recruiting
- Cooper University Hospital
-
Contact:
- Vineet Bhandari, MD, DM
- Phone Number: 1006156 856-342-2000
- Email: Bhandari-vineet@cooperhealth.edu
-
Contact:
- Faye Shapiro, MS, LCGC
- Phone Number: 856-541-6213
- Email: shapiro-faye@cooperhealth.edu
-
Principal Investigator:
- Vineet Bhandari, MD, DM
-
-
Texas
-
Edinburg, Texas, United States, 78539
- Recruiting
- The Women's Hospital at Renaissance
-
Contact:
- Luis Cantu
- Phone Number: 956-362-2396
- Email: Lu.Cantu@dhr-rgv.com
-
Contact:
- Dynio Honrubia, MD
- Phone Number: 956-802-8855
-
Principal Investigator:
- Dynio Honrubia, MD
-
El Paso, Texas, United States, 79938
- Not yet recruiting
- The Hospitals of Providence
-
Contact:
- Dhruv Gupta, MD
- Phone Number: 313-896-8168
- Email: dhruv.gupta@pediatrix.com
-
Contact:
- Jenifer Gehlsen, MD
- Email: jenifer.gehlsen@pediatrix.com
-
Principal Investigator:
- Dhruv Gupta, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Newborns presenting with probable genetic conditions inpatient on the NICU. These may include (but is not limited to) those with unexplained hypotonia, seizures, metabolic disorders, disorders of sex development, interstitial lung disease, immunodeficiency or multiple congenital anomalies.
- Babies must have at least one biologic parent available for consent and participation.
- The criteria for inclusion are 100% phenotype based and do not include any demographic parameters.
Exclusion Criteria:
- Presence of a likely nongenetic explanation for the phenotype (e.g., perinatal asphyxia explained by uterine rupture or placental pathology;
- Clinical features pathognomonic for a recognizable chromosomal abnormality, such as trisomy 21;
- Associations already known to have low genetic diagnostic yield, including VATER/VACTERL association and OEIS complex;
- Infants who die before enrollment;
- Known family history of genetic disease that is plausibly the cause of the infant's illness; - Those with a prenatal genetic diagnosis.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Neonates and Parents/Caregivers
Providers caring for newborns that meet eligibility criteria will approach parents to assess interest. The VIGOR study staff will remotely contact parents to complete consent for genomic sequencing (GS). We will also invite 1 additional primary caregiver (e.g. father, co-mother etc.) to participate even if that caregiver is not biologically related to the child. We will administer surveys at baseline enrollment to assess sociodemographics, obstetrical history, family genetic history & mental health; within 1 week of disclosure of findings to assess satisfaction & mental health; & at 3 & 6 months to further assess mental health & newborn clinical outcomes. We will approach a subset of the families for qualitative interviews to assess satisfaction with VIGOR & receipt of GS results with their physician in more detail. |
Clinicians
Following focus groups at each of the participating sites to assess the feasibility & needs of each site, the care teams will receive basic training in genomics and how to disclose GS results with VIGOR support.
Study orientation will be completed as part of the training.
Focus groups will be conducted within 1 year post implementation & again between year 4 & the completion of the study, to assess feasibility & appropriateness of VIGOR.
We will administer brief surveys to the care providers before & after receipt of genomic education to assess their baseline knowledge & comfort with genomic medicine in newborns.
Surveys will be repeated within a week of disclosure to families regarding feedback on the process & satisfaction with VIGOR.
After approximately 3-5 disclosure events, study staff will approach the clinical care team members to participate in a qualitative interview to assess their perspectives in more depth.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Implementation of VIGOR
Time Frame: 4 year
|
Penetration of VIGOR measured by percentage of eligible participants who were enrolled, tested, providers received CIR and completed a disclosure session.
|
4 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Implementation of VIGOR
Time Frame: 4 year
|
Appropriateness of VIGOR measured at the provider level by conducting focus groups/interviews.
|
4 year
|
Implementation of VIGOR
Time Frame: 4 year
|
Feasibility of VIGOR measured at the provider level by conducting focus groups/interviews.
|
4 year
|
Service Outcomes
Time Frame: 4 years
|
Equity in penetration of VIGOR use by race/ethnicity, insurance status and primary language measured at the participant level by conducting chart reviews and surveys.
|
4 years
|
Client Outcomes
Time Frame: 4 years
|
Function measured at the infant/caregiver and provider level by conducting surveys, chart reviews and focus groups/interviews.
|
4 years
|
Client Outcomes
Time Frame: 4 years
|
Symptomatology measured at the infant/caregiver level by conducting surveys, and interviews.
|
4 years
|
Client Outcomes
Time Frame: 4 years
|
Satisfaction measured at the infant/caregiver and provider level by conducting surveys, chart reviews and focus groups/interviews.
|
4 years
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Timothy Yu, MD, PhD, Boston Children's Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB-P00040496
- 1R01HG011798-01A1 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Genetic Predisposition to Disease
-
National Cancer Institute (NCI)RecruitingCancer | Hereditary Neoplasms | Genetic Predisposition to Cancer | EnvironmentUnited States
-
National Cancer Institute (NCI)Active, not recruitingCancer | Hereditary Neoplasms | Genetic Predisposition to Cancer | EnvironmentUnited States
-
St. Jude Children's Research HospitalRecruitingGenetic PredispositionUnited States
-
MedneonEnrolling by invitation
-
Eunice Kennedy Shriver National Institute of Child...CompletedGenetic PredispositionUnited States
-
University of VirginiaCompleted
-
Children's Hospital of PhiladelphiaNational Institutes of Health (NIH); National Human Genome Research Institute...Recruiting
-
University of VirginiaActive, not recruiting
-
The University of Texas Health Science Center at...Not yet recruiting
-
Centre Georges Francois LeclercRecruitingCancer | Genetic PredispositionFrance