Table 1.
Personal details and contact preferencesa,b |
Granular, Dynamic Consent choicesa,b,c |
Access to patient surveysa |
Study updates and news |
Two-way communication between participants and researchersa |
Consent guidesb,c |
Patient foruma |
Educational materialsc |
Self-reported health informationa,b |
Representation of genomic testing results |
Other research participation opportunitiesb |
Tracking function for research samples and data |
Features in bold texts were selected for inclusion.
aRef. [20].
bhttps://www.peerplatform.org/.
cRef. [22].