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Social media use among patients and caregivers: a scoping review

Hamm MP, Chisholm A, Shulhan J, Milne A, Scott SD, Given LM, Hartling L

BMJ open · 159 citas

Cómo se estudió

Diseño
Revisión sistemática (clasificado por nuestro filtro de IA)
Estudiado en
Personas
Resultado principal
Sin resultado de salud

Quién lo pagó

Financiación
Financiación independiente
Gobierno
Canadian Institutes of Health Research

Según 1 financiador declarado.

Publicación

Publicado
2013-01-01 · BMJ Open · vol. 3 · número 5 · pág. e002819
Editorial
BMJ
Citado
360 citas · más que el 100% de estudios similares · 29.7× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
31 trabajos
Acceso
Acceso abierto (revista) · CC-BY-NC
Áreas de investigación
Social Media in Health Education · Health Literacy and Information Accessibility · Mobile Health and mHealth Applications
Palabras clave
social media, patient populations, caregivers, online health communities, forum, social networking sites, virtual worlds, self-care, effectiveness evaluation, cancer

7 autores

  • Michele P Hamm🇨🇦 · autor de correspondenciaUniversity of Alberta
  • Annabritt Chisholm🇨🇦University of Alberta
  • Jocelyn Shulhan🇨🇦University of Alberta
  • Andrea Milne🇨🇦University of Alberta
  • Shannon D. Scott🇨🇦University of Alberta
  • Lisa M. Given🇦🇺Charles Sturt University
  • Lisa Hartling🇨🇦University of Alberta

Resumen

El texto original del estudio, en el idioma en que se publicó.

Objective

To map the state of the existing literature evaluating the use of social media in patient and caregiver populations.

Design

Scoping review.

Data sources

Medline, CENTRAL, ERIC, PubMed, CINAHL Plus Full Text, Academic Search Complete, Alt Health Watch, Health Source, Communication and Mass Media Complete, Web of Knowledge and ProQuest (2000-2012).

Study selection

Studies reporting primary research on the use of social media (collaborative projects, blogs/microblogs, content communities, social networking sites, virtual worlds) by patients or caregivers.

Data extraction

Two reviewers screened studies for eligibility; one reviewer extracted data from relevant studies and a second performed verification for accuracy and completeness on a 10% sample. Data were analysed to describe which social media tools are being used, by whom, for what purpose and how they are being evaluated.

Results

Two hundred eighty-four studies were included. Discussion forums were highly prevalent and constitute 66.6% of the sample. Social networking sites (14.8%) and blogs/microblogs (14.1%) were the next most commonly used tools. The intended purpose of the tool was to facilitate self-care in 77.1% of studies. While there were clusters of studies that focused on similar conditions (eg, lifestyle/weight loss (12.7%), cancer (11.3%)), there were no patterns in the objectives or tools used. A large proportion of the studies were descriptive (42.3%); however, there were also 48 (16.9%) randomised controlled trials (RCTs). Among the RCTs, 35.4% reported statistically significant results favouring the social media intervention being evaluated; however, 72.9% presented positive conclusions regarding the use of social media.

Conclusions

There is an extensive body of literature examining the use of social media in patient and caregiver populations. Much of this work is descriptive; however, with such widespread use, evaluations of effectiveness are required. In studies that have examined effectiveness, positive conclusions are often reported, despite non-significant findings.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial (CC BY-NC).

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