Literature DB >> 33779756

Feasibility of Medical Student Mentors to Improve Transition in Sickle Cell Disease.

Adrienne S Viola1,2,3, Richard Drachtman1, Amanda Kaveney2, Ashwin Sridharan2, Beth Savage1, Cristine D Delnevo3, Elliot J Coups1, Jerlym S Porter4, Katie A Devine1.   

Abstract

OBJECTIVE: Advances in medical care have resulted in nearly 95% of all children with sickle cell disease (SCD) living to adulthood. There is a lack of effective transition programming, contributing to high rates of mortality and morbidity among adolescents and young adults (AYAs) during the transition from pediatric to adult healthcare. This nonrandomized study evaluated the feasibility, acceptability, and preliminary outcomes of a novel medical student mentor intervention to improve transition outcomes for AYA with SCD.
METHODS: Eligible participants were ages 18-25 years, either preparing for transition or had transferred to adult care within the past year. Twenty-four AYA with SCD (Mage = 20.3, SD = 2.6) enrolled in the program and were matched with a medical student mentor. Feasibility and acceptability of the intervention was assessed through enrollment rates, reasons for refusal, retention rates, engagement with the intervention, satisfaction, and reasons for drop-out. Dependent t-tests were used to evaluate the preliminary effects of the intervention on patient transition readiness, health-related quality of life, self-efficacy, SCD knowledge, medication adherence, and health literacy.
RESULTS: Participants (N = 24) demonstrated adequate retention (75.0%), adherence to the intervention (M = 5.3 of 6 sessions), and satisfaction with the intervention components. Participants demonstrated significant improvements in transition readiness (p = .001), self-efficacy (p = .002), medication adherence (p = .02), and health literacy (p = .05).
CONCLUSIONS: A medical student mentor intervention to facilitate transition from pediatric to adult care for AYA with SCD is both feasible and acceptable to patients and medical students. Preliminary results suggest benefits for patients, warranting a larger efficacy study.
© The Author(s) 2021. Published by Oxford University Press on behalf of the Society of Pediatric Psychology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  adolescents; emerging/young adults; pilot/feasibility trial; sickle cell disease; social functioning and peers

Mesh:

Year:  2021        PMID: 33779756      PMCID: PMC8291672          DOI: 10.1093/jpepsy/jsab031

Source DB:  PubMed          Journal:  J Pediatr Psychol        ISSN: 0146-8693


  34 in total

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Authors:  Samuel N Rodgers-Melnick; Tara J Griest Pell; Deforia Lane; Coretta Jenerette; Pingfu Fu; Seunghee Margevicius; Jane A Little
Journal:  Int J Adolesc Med Health       Date:  2017-08-05

2.  Measuring Transition Readiness: A Correlational Study of Perceptions of Parent and Adolescents and Young Adults with Sickle Cell Disease.

Authors:  Barbara Speller-Brown; Katherine Patterson Kelly; Brigit VanGraafeiland; Suzanne Feetham; Anne Sill; Deepika Darbari; Emily R Meier
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4.  Development of quality indicators for transition from pediatric to adult care in sickle cell disease: A modified Delphi survey of adult providers.

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6.  Identification of risk factors for an unsuccessful transition from pediatric to adult sickle cell disease care.

Authors:  Biree Andemariam; Jasmine Owarish-Gross; James Grady; Donna Boruchov; Roger S Thrall; J Nathan Hagstrom
Journal:  Pediatr Blood Cancer       Date:  2013-12-18       Impact factor: 3.167

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Authors:  Carlton Haywood; Sophie Lanzkron; Shawn Bediako; John J Strouse; Jennifer Haythornthwaite; C Patrick Carroll; Marie Diener-West; Gladys Onojobi; Mary Catherine Beach
Journal:  J Gen Intern Med       Date:  2014-09-10       Impact factor: 5.128

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Authors:  Gayelene Boardman; Terence McCann; Debra Kerr
Journal:  J Adv Nurs       Date:  2014-03-16       Impact factor: 3.187

9.  Disease Self-Efficacy and Health-Related Quality of Life in Adolescents With Sickle Cell Disease.

Authors:  Alana Goldstein-Leever; James L Peugh; Charles T Quinn; Lori E Crosby
Journal:  J Pediatr Hematol Oncol       Date:  2020-03       Impact factor: 1.170

10.  The iPeer2Peer Program: a pilot randomized controlled trial in adolescents with Juvenile Idiopathic Arthritis.

Authors:  Jennifer Stinson; Sara Ahola Kohut; Paula Forgeron; Khush Amaria; Mary Bell; Miriam Kaufman; Nadia Luca; Stephanie Luca; Lauren Harris; Charles Victor; Lynn Spiegel
Journal:  Pediatr Rheumatol Online J       Date:  2016-09-02       Impact factor: 3.054

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