Evidence map›Paper›PMID 34851295›Full record

ArticleJMIR formative research2021

Preferences for Using a Mobile App in Sickle Cell Disease Self-management: Descriptive Qualitative Study.

Tilicia L Mayo-Gamble, Delores Quasie-Woode, Jennifer Cunningham-Erves, Margo Rollins, David Schlundt, Kemberlee Bonnet, Velma McBride Murry

Abstract read
In one paragraph

Article in JMIR formative research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

7 authors.

Tilicia L Mayo-GambleDepartment of Health Policy and Community Health, Jiann-Ping Hsu College of Public Health, Georgia Southern University, Statesboro, GA, United States.ORCID https://orcid.org/0000-0002-9303-5266
Delores Quasie-WoodeCenter for Disease Control and Prevention Foundation, Atlanta, GA, United States.ORCID https://orcid.org/0000-0002-2684-6421
Jennifer Cunningham-ErvesDepartment of Internal Medicine, Meharry Medical College, Nashville, TN, United States.ORCID https://orcid.org/0000-0002-7780-9874
Margo RollinsDepartment of Pediatrics, Aflac Cancer and Blood Disorders Center, Emory University School of Medicine, Atlanta, GA, United States.ORCID https://orcid.org/0000-0002-7432-9752
David SchlundtDepartment of Psychological Sciences, College of Arts and Sciences, Vanderbilt University, Nashville, TN, United States.ORCID https://orcid.org/0000-0001-7069-9644
Kemberlee BonnetDepartment of Psychological Sciences, College of Arts and Sciences, Vanderbilt University, Nashville, TN, United States.ORCID https://orcid.org/0000-0003-4046-3408
Velma McBride MurryDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, TN, United States.ORCID https://orcid.org/0000-0003-2663-2738

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIndividuals with sickle cell disease (SCD) and their caregivers may benefit from technology-based resources to improve disease self-management.

objectiveThis study explores the preferences regarding a mobile health (mHealth) app to facilitate self-management in adults with SCD and their caregivers living in urban and rural communities.

methodsFive community listening sessions were conducted in 2 urban and rural communities among adults with SCD and their caregivers (N=43). Each session comprised 4 to 15 participants. Participants were asked questions on methods of finding information about SCD self-care, satisfaction with current methods for finding SCD management information, support for SCD management, important features for development of an mHealth app, and areas of benefit for using an mHealth app for SCD self-management. An inductive-deductive content analysis approach was implemented to identify the critical themes.

resultsSeven critical themes emerged, including the current methods for receiving self-management information, desired information, recommendations for communicating sickle cell self-management information, challenges of disease management, types of support received for disease management, barriers to and facilitators of using an mHealth app, and feature preferences for an mHealth app. In addition, we found that the participants were receptive to using mHealth apps in SCD self-management.

conclusionsThis study expands our knowledge on the use of mHealth technology to reduce information access barriers pertaining to SCD. The findings can be used to develop a patient-centered, user-friendly mHealth app to facilitate disease self-management, thus increasing access to resources for families of patients with SCD residing in rural communities.

Indexed as

digital technologyhealth outcomeshematologymHealth appmobile healthmobile phonepatient-centered technologyruralsickle cell disease

Identifiers

PMID34851295
PMCPMC8672290

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Registered trials

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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.