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What is needed to obtain informed consent and monitor capacity for a successful study involving People with Mild Dementia?: Our experience in a multi-centre study

Strategies on informed consent process and capacity monitoring for mild dementia research are at developing state. We reflected on our experience and found that the successful collection of informed consent and full participation of PwD required the involvement of familiar healthcare professionals/care workers/staff at the recruitment and data collection stages and this needs to occur in an active support environment. Time is another important factor affecting the success of the study.

Identiferoai:union.ndltd.org:DRESDEN/oai:qucosa:de:qucosa:36687
Date19 December 2019
CreatorsLim, Jennifer NW, Almeida, Rosa, Holthoff-Detto, Vjera, Ludden, Geke DS, Smith, Tina, Niedderer, Kristina
PublisherTUDpress
Source SetsHochschulschriftenserver (HSSS) der SLUB Dresden
LanguageEnglish
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, doc-type:conferenceObject, info:eu-repo/semantics/conferenceObject, doc-type:Text
Rightsinfo:eu-repo/semantics/openAccess
Relation978-3-95908-183-2, urn:nbn:de:bsz:14-qucosa2-353220, qucosa:35322

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