Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
200 participants
INTERVENTIONAL
2022-02-28
2025-07-30
Brief Summary
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Hypotheses are fully described in the protocol. The primary hypothesis is that 80% of recruited child-proxy dyads will have at least one RTC-enabled PeLTQL score at 12 months. Other hypotheses look at implementation metrics and patient outcomes.
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Detailed Description
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The Pediatric Liver Transplant Quality of Life (PeLTQL), the study measure, is a condition-specific 26-item questionnaire; the investigators will be evaluating both total scores as well as subdomain scores and, importantly, discrepancies between child and parent reports of the child's QOL.
The Electronic Platform: Real-Time Clinic (RTC). The platform will furnish providers with the total scores, subscale scores, thresholds ("met" vs. "not met"), discrepancy scores, and any question that has scores which may concern the clinician/clinical team.
This information will be available before the clinic visit and can guide and inform discussion and problem-solving between patient and clinical team. The study does not standardize the response to the results and will not suggest a preferred way of action. Interpretation of the results, as well as actions related to them are completely left to clinician's discretion.
The setting of this study - the Starzl Network for Excellence in Pediatric Transplantation (SNEPT Centers). SNEPT is a learning healthcare network that was established in 2018 to accelerate improvement in transplant outcomes by incorporating innovation, technology and the patient voice to address gaps in care that were identified by the collaborative transplant centers and family representatives.
Study Aims
The primary aim is successful implementation of the RTC app-based tool to obtain PeLTQL scores from pediatric liver transplant recipients and their parents or caregivers.
The investigators also aim to assess the usability, impact, and ease of use (both for clinicians and patients/families) of the RTC platform and app-based version of the PeLTQL. The investigators will evaluate clinicians' subjective views on the platforms' ease of use, their time spent evaluating results, both in clinic and before patient visits, as well as the app's impact on back-end clinic workflow.
Impact on patient outcomes will be evaluated using pre-post comparisons on adherence (determined by the objective medication level variability index, MLVI) as well as on the PeLTQL.
Conditions
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Study Design
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NA
SINGLE_GROUP
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Pediatric liver transplant recipients
As this is a single arm trial, all eligible liver transplant recipients and their caregivers will be enrolled in this arm.
Eligible participants are children who received a liver transplant at least 1 year prior to enrollment at a participating SNEPT center and continue to receive their post-transplant care at that center.
PeLTQL delivery via electronic means
Delivery of PeLTQL scoring information to clinicians via electronic means.
Interventions
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PeLTQL delivery via electronic means
Delivery of PeLTQL scoring information to clinicians via electronic means.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
1. The patient is \> 8 at enrollment and \< 20 years of age at 2 year post enrollment.
2. The patient received a liver transplantation at least 1 year prior to enrollment.
3. The patient and parent/ guardian have internet access either through a smartphone, tablet or computer.
4. The patient and at least one guardian speaks English or Spanish at a level that allows them to understand the study procedures and consent to the study.
Exclusion Criteria
1. The patient is expected to transition to another service (e.g., adult clinic, another hospital) in the year following enrollment.
2. The guardian or patient (in a developmentally-appropriate manner) do not understand the study procedures. This will be verified by asking both guardian and adolescent to repeat the study procedures.
8 Years
20 Years
ALL
No
Sponsors
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Icahn School of Medicine at Mount Sinai
OTHER
The Hospital for Sick Children
OTHER
Emory-Children's Center
OTHER
Columbia University
OTHER
Seattle Children's Hospital
OTHER
University of San Francisco
OTHER
University of Pittsburgh
OTHER
Responsible Party
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George Mazariegos
Professor of Surgery, Chief Pediatric Transplantation
Principal Investigators
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Eyal Shemesh, MD
Role: PRINCIPAL_INVESTIGATOR
Icahn School of Medicine at Mt. Sinai
George Mazariegos, MD
Role: PRINCIPAL_INVESTIGATOR
University of Pittsburgh
Locations
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UCSF Benioff Children's Hospital
Oakland, California, United States
Emory Children's
Atlanta, Georgia, United States
Columbia University Children's
New York, New York, United States
Mt. Sinai
New York, New York, United States
UPMC Children's
Pittsburgh, Pennsylvania, United States
Seattle Children's
Seattle, Washington, United States
Toronto Sick Kids
Toronto, Ontario, Canada
Countries
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References
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Ng V, Nicholas D, Dhawan A, Yazigi N, Ee L, Stormon M, Gilmour S, Schreiber R, Taylor R, Otley A; PeLTQL study group. Development and validation of the pediatric liver transplantation quality of life: a disease-specific quality of life measure for pediatric liver transplant recipients. J Pediatr. 2014 Sep;165(3):547-55.e7. doi: 10.1016/j.jpeds.2014.05.024. Epub 2014 Jun 26.
Related Links
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Starzl Network Main Website
Other Identifiers
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STUDY21090139
Identifier Type: -
Identifier Source: org_study_id
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