Using the consolidated framework for implementation research to guide a pilot of implementing an institution level patient informed consent process for clinical research at an outpatient setting.
Xuling LinJoanne Yong Ern YuenWei Quan Jeremy ChanTushar Gosavi DivakarNicole Chwee Har KeongLester Chee How LeeSumeet KumarChew Seah TanKim Chin Pauline SoonYee Pheng Amy ChewHeriati Mohd YazidFarah Julieanna Mohd SalehFenglong CaiFui Chih ChaiNur Fakhirah Mohamed AzwanNurhidayah Mohamad FaizalSiew Choo LouSiew Sin Priscilla TanCut Marini JariminGowri Michael StanleyKhadijah HussienNurhazah SanmwanNur Hidayah AmranNurliana RamliShermyn Xiu Min NeoLouis Chew Seng TanEng King TanElaine P M LumPublished in: Pilot and feasibility studies (2023)
Our findings support the feasibility of implementing an institution level informed consent workflow that integrates with service operations at the outpatient setting to optimize healthcare resources for research. The CFIR provided a useful framework to identify barriers and facilitators in the design of the intervention and its implementation process.