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Accepted for/Published in: JMIR Pediatrics and Parenting

Date Submitted: May 4, 2018
Open Peer Review Period: May 9, 2018 - May 30, 2018
Date Accepted: Jun 15, 2018
(closed for review but you can still tweet)

The final, peer-reviewed published version of this preprint can be found here:

Online Peer-to-Peer Mentoring Support for Youth with Hemophilia: Qualitative Needs Assessment

Breakey VR, Bouskill V, Nguyen C, Luca S, Stinson JN, Ahola Kohut S

Online Peer-to-Peer Mentoring Support for Youth with Hemophilia: Qualitative Needs Assessment

JMIR Pediatr Parent 2018;1(2):e10958

DOI: 10.2196/10958

PMID: 31518296

PMCID: 6715049

Online Peer-to-Peer Mentoring Support for Youth with Hemophilia: Qualitative Needs Assessment

  • Vicky R Breakey; 
  • Vanessa Bouskill; 
  • Cynthia Nguyen; 
  • Stephanie Luca; 
  • Jennifer N Stinson; 
  • Sara Ahola Kohut

ABSTRACT

Background:

To support adolescents through transition from pediatrics to adult care, health care providers and families help teens gain knowledge and develop self-management skills. Peer mentoring can provide meaningful support and has been associated with improved health outcomes in patients with other chronic conditions. Peer mentoring is an appealing way to provide support, but it is imperative to consider the unique needs of adolescents to ensure its success.

Objective:

The objective of our study was to identify the peer mentoring wants and needs of youth with hemophilia in order to guide the development of a new program.

Methods:

In this qualitative study, we interviewed a convenience sample of youth with hemophilia from 2 Canadian hemophilia treatment centers. Two iterative cycles of audiorecorded, semistructured individual interviews were conducted. Descriptive statistics and content analyses were used to organize data into categories that reflected emerging themes.

Results:

In total, we recruited 23 participants aged 12-20 years, with a mean age of 14.91 (2.57) years. When asked about program design, participants weighed the importance of flexibility in delivery (eg, Web-based, in person, text messaging [short message service]), content (eg, structured vs unstructured), frequency of sessions, and length of the program. Participants identified some potential challenges such as scheduling issues, comfort level for disease discussion, and discordant mentor-mentee personality types. The program was viewed as a positive medium for connecting peers with hemophilia.

Conclusions:

Adolescents with hemophilia expressed interest in a peer mentoring program and provided valuable insight that will be applied in the development of a peer mentoring program for youth with hemophilia.


 Citation

Please cite as:

Breakey VR, Bouskill V, Nguyen C, Luca S, Stinson JN, Ahola Kohut S

Online Peer-to-Peer Mentoring Support for Youth with Hemophilia: Qualitative Needs Assessment

JMIR Pediatr Parent 2018;1(2):e10958

DOI: 10.2196/10958

PMID: 31518296

PMCID: 6715049

Per the author's request the PDF is not available.

© The authors. All rights reserved. This is a privileged document currently under peer-review/community review (or an accepted/rejected manuscript). Authors have provided JMIR Publications with an exclusive license to publish this preprint on it's website for review and ahead-of-print citation purposes only. While the final peer-reviewed paper may be licensed under a cc-by license on publication, at this stage authors and publisher expressively prohibit redistribution of this draft paper other than for review purposes.