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ArticleJMIR research protocols2025

The Community Health Workers and Mobile Health for Emerging Adults Transitioning Sickle Cell Disease Care (COMETS) Trial: Protocol for a Randomized Controlled Trial.

Tanisha D Belton, Caren M Steinway, Olivia Teng, Justine Shults, Lamia P Barakat, Banu Aygun, Abena Appiah-Kubi, Lori E Crosby, Omar Niss, Biree Andemariam and 7 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in JMIR research protocols, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03648710 (Community Health Workers and Mobile Health for Emerging Adults Transitioning Sickle Cell Disease Care), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03648710 nacompletednot on this map

Community Health Workers and Mobile Health for Emerging Adults Transitioning Sickle Cell Disease Care

TypeinterventionalSponsorChildren's Hospital of PhiladelphiaRan2019 to 2024Enrolled405ConditionsSickle Cell DiseaseArmsPeer Community Health Worker, Mobile Health
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Tanisha D Belton *PolicyLab, Division of General Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.ORCID 0009-0003-8570-513X
Caren M Steinway *Department of Pediatrics, Northwell Health, New Hyde Park, NY, United States.ORCID 0000-0003-0169-7105
Olivia TengDepartment of Pediatrics, Northwell Health, New Hyde Park, NY, United States.ORCID 0009-0005-6041-0575
Justine ShultsDepartment of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.ORCID 0000-0002-0266-0980
Lamia P BarakatDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA, United States.ORCID 0000-0002-0938-4712
Banu AygunPediatric Hematology Oncology and Stem Cell Transplantation, Cohen Children's Medical Center, New Hyde Park, NY, United States.ORCID 0000-0001-9934-5161
Abena Appiah-KubiPediatric Hematology Oncology and Stem Cell Transplantation, Cohen Children's Medical Center, New Hyde Park, NY, United States.ORCID 0000-0001-8147-3624
Lori E CrosbyBehavioral Medicine and Clinical Psychology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.ORCID 0000-0001-6656-7745
Omar NissDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.ORCID 0000-0003-4157-4644
Biree AndemariamNew England Sickle Cell Institute, University of Connecticut Health, Farmington, CT, United States.ORCID 0000-0002-2540-6037
Lisa A SchwartzDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA, United States.ORCID 0000-0002-7034-9553
Samantha LumaDepartment of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.ORCID 0009-0000-1832-6613
Kyle A SmithDepartment of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.ORCID 0009-0003-2894-3457
Tracey B JohnsonDepartment of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.ORCID 0009-0004-8167-1224
David M RubinPolicyLab, Division of General Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.ORCID 0009-0009-8039-5236
Kim M Smith-WhitleyDivision of General Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.ORCID 0000-0002-2790-411X
Sophia JanDepartment of Pediatrics, Northwell Health, New Hyde Park, NY, United States.ORCID 0000-0002-1796-6464

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTransitioning from pediatric to adult sickle cell disease (SCD) care is challenging for emerging adults (aged 17-25 years). This period is marked by a 7-fold increase in mortality rates and has the highest rates of hospitalizations, emergency room visits, and hospital readmissions compared with children living with SCD. These challenges are exacerbated by fragmented care coordination, difficulty navigating adult health care systems, and increased self-management responsibilities.

objectiveThis study aims to compare the effectiveness of 2 interventions designed to support emerging adults living with SCD during this transition: a mobile health (mHealth) app and community health worker (CHW) support to standard care.

methodsThe Community Health Workers and Mobile Health for Emerging Adults Transitioning Sickle Cell Disease Care (COMETS) trial is an ongoing multicenter, 3-arm, open-label randomized controlled trial; 375 emerging adults (aged 17-25 years) are being enrolled and randomized 1:1:1 to (1) a 6-month CHW intervention focused on self-management skills, symptom tracking, care coordination, and transition planning; (2) a 6-month mHealth self-management program (enhanced iManage application) with tailored SMS text messaging (THRIVE [Texting Health-Related Resources to Inform, Motivate, and Engage] 2.0); or (3) enhanced usual care (control). Participants are followed for 18 months. The primary outcome is the change in self-reported health-related quality of life assessed using the PedsQL SCD module. Secondary outcomes include acute care use (hospitalizations and emergency department visits), patient activation, self-management behavior, and successful transfer to adult hematology care.

resultsThe institutional review board at Children's Hospital of Philadelphia approved this study in June 2018. Recruitment began in January 2019 and ended in December 2022; we completed data collection in November 2024. We have enrolled a total of 405 participants.

conclusionsThis trial addresses a critical gap in transition intervention research for young adults with SCD. It will provide evidence on the comparative effectiveness of 2 promising interventions (CHW and mHealth) and inform the development of scalable and sustainable transition support programs. Findings will have implications for improving health-related quality of life, reducing acute care use, and promoting successful transition to adult-centered SCD care for this vulnerable population.

trial registrationClinicalTrials.gov NCT03648710; https://clinicaltrials.gov/study/NCT03648710. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/69239.

Indexed as

Anemia, Sickle CellCommunity Health WorkersTransition to Adult CareAdolescentAdultFemaleHumansMaleMulticenter Studies as TopicQuality of LifeRandomized Controlled Trials as TopicTelemedicineYoung Adultadolescents and young adultscommunity health workerhealth care transitionmHealthmobile healthmobile phonepediatricsquality of lifeself-managementsickle cell disease

Identifiers

PMID40905609
PMCPMC12447008

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.