Many research participants are willing to be contacted about future research opportunities, however this question is not always asked. Furthermore, if participants do consent for contact about future research, this information is not always accessible to other research teams. We discuss our experience of recruiting individuals who have previously taken part in healthcare research and suggest potential strategies to support this process and enable greater research participation
Abstract Background EHR phenotyping offers the ability to rapidly assemble a precisely defined cohor...
This work was supported in part by a grant from Scotland’s Chief Scientist Office (CZG/2/509) and ad...
The public needs to be included in debates about what is, and isn't, in its best interests. Until th...
Are you struggling to support participant recruitment at your institution? Are you concerned that no...
Background. Equitable access to research studies needs to be increased for all patients. There is de...
Objectives: To develop a new model for patient recruitment that harnessed the full potential of Elec...
Background: The NHS pledges to give all patients access to clinical research. In England, 32% of Gen...
ObjectiveClinical trials and studies in intensive care units (ICUs) have complex consent processes a...
Objectives: To develop a new model for patient recruitment that harnessed the full potential of Elec...
BackgroundFew studies have examined the effects of Institutional Review Board (IRB) requirements to ...
OBJECTIVES: To describe our experience of using a confidentiality waiver (Section 251) in the Nation...
Plain English summary Increasingly, funders and researchers want to partner with patients in health ...
Objective Clinical trials and studies in intensive care units (ICUs) have complex consent processes ...
Abstract Background A research register (Reach West) has been established to facilitate recruitment ...
BackgroundDifficulties with recruitment pose a major, increasingly recognised challenge to the viabi...
Abstract Background EHR phenotyping offers the ability to rapidly assemble a precisely defined cohor...
This work was supported in part by a grant from Scotland’s Chief Scientist Office (CZG/2/509) and ad...
The public needs to be included in debates about what is, and isn't, in its best interests. Until th...
Are you struggling to support participant recruitment at your institution? Are you concerned that no...
Background. Equitable access to research studies needs to be increased for all patients. There is de...
Objectives: To develop a new model for patient recruitment that harnessed the full potential of Elec...
Background: The NHS pledges to give all patients access to clinical research. In England, 32% of Gen...
ObjectiveClinical trials and studies in intensive care units (ICUs) have complex consent processes a...
Objectives: To develop a new model for patient recruitment that harnessed the full potential of Elec...
BackgroundFew studies have examined the effects of Institutional Review Board (IRB) requirements to ...
OBJECTIVES: To describe our experience of using a confidentiality waiver (Section 251) in the Nation...
Plain English summary Increasingly, funders and researchers want to partner with patients in health ...
Objective Clinical trials and studies in intensive care units (ICUs) have complex consent processes ...
Abstract Background A research register (Reach West) has been established to facilitate recruitment ...
BackgroundDifficulties with recruitment pose a major, increasingly recognised challenge to the viabi...
Abstract Background EHR phenotyping offers the ability to rapidly assemble a precisely defined cohor...
This work was supported in part by a grant from Scotland’s Chief Scientist Office (CZG/2/509) and ad...
The public needs to be included in debates about what is, and isn't, in its best interests. Until th...