Literature DB >> 28164178

Care Partnerships: Toward Technology to Support Teens' Participation in Their Health Care.

Matthew K Hong1, Lauren Wilcox1, Daniel Machado1, Thomas A Olson2, Stephen F Simoneaux2.   

Abstract

Adolescents with complex chronic illnesses, such as cancer and blood disorders, must partner with family and clinical caregivers to navigate risky procedures with life-altering implications, burdensome symptoms and lifelong treatments. Yet, there has been little investigation into how technology can support these partnerships. We conducted 38 in-depth interviews (15 with teenage adolescents with chronic forms of cancer and blood disorders, 15 with their parents, and eight with clinical caregivers) along with nine non-participant observations of clinical consultations to better understand common challenges and needs that could be supported through design. Participants faced challenges primarily concerning: 1) teens' limited participation in their care, 2) communicating emotionally-sensitive information, and 3) managing physical and emotional responses. We draw on these findings to propose design goals for sociotechnical systems to support teens in partnering in their care, highlighting the need for design to support gradually evolving partnerships in care.

Entities:  

Keywords:  Adolescents; Chronic Illnesses; Families; Health Information Management; Personal Health; Self-Management

Year:  2016        PMID: 28164178      PMCID: PMC5291175          DOI: 10.1145/2858036.2858508

Source DB:  PubMed          Journal:  Proc SIGCHI Conf Hum Factor Comput Syst


  29 in total

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2.  A consensus statement on health care transitions for young adults with special health care needs.

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Journal:  Pediatrics       Date:  2002-12       Impact factor: 7.124

Review 3.  Self-management approaches for people with chronic conditions: a review.

Authors:  Julie Barlow; Chris Wright; Janice Sheasby; Andy Turner; Jenny Hainsworth
Journal:  Patient Educ Couns       Date:  2002 Oct -Nov

Review 4.  Self-management education: history, definition, outcomes, and mechanisms.

Authors:  Kate R Lorig; Halsted Holman
Journal:  Ann Behav Med       Date:  2003-08

5.  Chronically ill adolescents' experiences of communicating with doctors: a qualitative study.

Authors:  Bryony A Beresford; Patricia Sloper
Journal:  J Adolesc Health       Date:  2003-09       Impact factor: 5.012

Review 6.  Doctor-parent-child communication. A (re)view of the literature.

Authors:  K Tates; L Meeuwesen
Journal:  Soc Sci Med       Date:  2001-03       Impact factor: 4.634

7.  Bias influencing maternal reports of child behaviour and emotional state.

Authors:  J M Najman; G M Williams; J Nikles; S Spence; W Bor; M O'Callaghan; R Le Brocque; M J Andersen; G J Shuttlewood
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2001-04       Impact factor: 4.328

8.  Deaths attributed to pediatric complex chronic conditions: national trends and implications for supportive care services.

Authors:  C Feudtner; R M Hays; G Haynes; J R Geyer; J M Neff; T D Koepsell
Journal:  Pediatrics       Date:  2001-06       Impact factor: 7.124

Review 9.  Can parents rate their child's health-related quality of life? Results of a systematic review.

Authors:  C Eiser; R Morse
Journal:  Qual Life Res       Date:  2001       Impact factor: 4.147

10.  Psychological outcomes in long-term survivors of childhood leukemia, Hodgkin's disease, and non-Hodgkin's lymphoma: a report from the Childhood Cancer Survivor Study.

Authors:  Brad J Zebrack; Lonnie K Zeltzer; John Whitton; Ann C Mertens; Lorrie Odom; Roger Berkow; Leslie L Robison
Journal:  Pediatrics       Date:  2002-07       Impact factor: 9.703

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  7 in total

1.  Adolescent and Caregiver use of a Tethered Personal Health Record System.

Authors:  Matthew K Hong; Lauren Wilcox; Clayton Feustel; Karen Wasileski-Masker; Thomas A Olson; Stephen F Simoneaux
Journal:  AMIA Annu Symp Proc       Date:  2017-02-10

2.  Title: The Children's Oncology Planning for Emergencies (COPE) Tool: Prototyping with Caregivers of Children with Cancer.

Authors:  Emily L Mueller; Anneli R Cochrane; Courtney M Moore; Andrew D Miller; Sarah E Wiehe
Journal:  AMIA Annu Symp Proc       Date:  2021-01-25

3.  Telehealth experiences of providers and patients who use augmentative and alternative communication.

Authors:  Erin Beneteau; Ann Paradiso; Wanda Pratt
Journal:  J Am Med Inform Assoc       Date:  2022-01-29       Impact factor: 4.497

4.  Children's Designs for the Future of Telehealth.

Authors:  Erin Beneteau; Ann Paradiso; Wanda Pratt
Journal:  AMIA Annu Symp Proc       Date:  2022-02-21

5.  Supporting Collaborative Health Tracking in the Hospital: Patients' Perspectives.

Authors:  Sonali R Mishra; Andrew D Miller; Shefali Haldar; Maher Khelifi; Jordan Eschler; Rashmi G Elera; Ari H Pollack; Wanda Pratt
Journal:  Proc SIGCHI Conf Hum Factor Comput Syst       Date:  2018-04-21

6.  Using Priorities of Hospitalized Patients and Their Caregivers to Develop Personas.

Authors:  Elena Agapie; Logan Kendall; Sonali R Mishra; Shefali Haldar; Maher Khelifi; Ari Pollack; Wanda Pratt
Journal:  AMIA Annu Symp Proc       Date:  2020-03-04

7.  Information Quality Challenges of Patient-Generated Data in Clinical Practice.

Authors:  Peter West; Max Van Kleek; Richard Giordano; Mark Weal; Nigel Shadbolt
Journal:  Front Public Health       Date:  2017-11-01
  7 in total

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