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This paper is in the following e-collection/theme issue:

Development and Evaluation of Research Methods, Instruments and Tools (854) mHealth for Symptom and Disease Monitoring, Chronic Disease Management (1850) Health Services Research (599) E-Health / Health Services Research and New Models of Care (825) Recruitment of Research Participants (396) Registered Report (881)

Published on in Vol 8 (2024)

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/48767, first published .
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Recruitment Strategies in the Integration of Mobile Health Into Sickle Cell Disease Care to Increase Hydroxyurea Utilization Study (meSH): Multicenter Survey Study

Recruitment Strategies in the Integration of Mobile Health Into Sickle Cell Disease Care to Increase Hydroxyurea Utilization Study (meSH): Multicenter Survey Study

Authors of this article:

Chinonyelum Nwosu1 Author Orcid Image ;   Hamda Khan1 Author Orcid Image ;   Rita Masese2 Author Orcid Image ;   Judith M Nocek3 Author Orcid Image ;   Siera Gollan4 Author Orcid Image ;   Taniya Varughese5 Author Orcid Image ;   Sarah Bourne6 Author Orcid Image ;   Cindy Clesca7 Author Orcid Image ;   Sara R Jacobs8 Author Orcid Image ;   Ana Baumann5 Author Orcid Image ;   Lisa M Klesges5 Author Orcid Image ;   Nirmish Shah2 Author Orcid Image ;   Jane S Hankins9 Author Orcid Image ;   Matthew P Smeltzer10 Author Orcid Image
Article Authors Cited by (2) Tweetations (7) Metrics

Journals

  1. Belton T, Carbaugh L, Stevens E, Seide A, Ferreira B, Teng O, Bennett L, Pfeiffer A, Ferreira M, Shova A, Arens R, Williford D, Aygun B, Appiah-Kubi A, Apollonsky N, Boruchov D, Niss O, Smith-Whitley K, Jan S, Steinway C. Recruitment and retention of young adults with sickle cell disease. Health Care Transitions 2026;4:100133 View
  2. Chukwudozie I, Nocek J, Farooqui M, Lasley P, Verda L, Sanders E, Reynolds B, Hsu L, Gordeuk V, Wandersman A, Saving K. Outcomes of a sustained multi-disciplinary advisory group in advancing sickle cell care and research. Journal of Sickle Cell Disease 2026;3(1) View