Study partners perform essential tasks in dementia research and can experience burdens and benefits in this role

Betty E Black, Holly Taylor, Peter V Rabins, Jason Karlawish

Research output: Contribution to journalArticle

Abstract

Most studies that enroll individuals with dementia require a study partner for each participant. Study partners—usually family members—perform several key roles: accompanying the participant to visits, providing information about the participant, and assisting with procedures such as taking medication. Little is known, however, about their experiences when performing these roles. Dementia researchers and institutional review boards need to know these experiences because the study partner role is one key factor in a study’s success. This prospective qualitative study, using up to three semi-structured interviews with 62 study partners involved in a range of dementia studies, documented their subjective experiences. Content analysis demonstrates that study partners perform a range of tasks—often within the context of being a caregiver—that enable cognitively impaired individuals to participate in dementia research. These tasks present study partners with unique burdens and benefits, some of which dementia researchers and institutional review boards can address.

Original languageEnglish (US)
Pages (from-to)494-514
Number of pages21
JournalDementia
Volume17
Issue number4
DOIs
StatePublished - May 1 2018

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dementia
experience
content analysis
medication
interview

Keywords

  • caregiver
  • dementia research
  • informant
  • study partner

ASJC Scopus subject areas

  • Sociology and Political Science
  • Social Sciences(all)

Cite this

Study partners perform essential tasks in dementia research and can experience burdens and benefits in this role. / Black, Betty E; Taylor, Holly; Rabins, Peter V; Karlawish, Jason.

In: Dementia, Vol. 17, No. 4, 01.05.2018, p. 494-514.

Research output: Contribution to journalArticle

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