Abstract Background Providing understandable information to patients is necessary to achieve the aims of the Informed Consent process: respecting and promoting patients’ autonomy and protecting patients from harm. In recent decades, new, primarily digital technologies have been used to apply and test innovative formats of Informed Consent. We conducted a systematic review to explore the impact of using digital tools for Informed Consent in both clinical research and in clinical practice. Understanding, satisfaction and participation were compared for digital tools versus the non-digital Informed Consent process. Methods We searched for studies on available electronic databases, including Pubmed, EMBASE, and Cochrane. Studies were identi...
Purpose: This study identifies best practices for informed consent for emergent computed tomography ...
Objective: To assess the efficacy, with respect to participant understanding of information, of a co...
To pursue scientific goals with patient data usually requires informed consent from the data subject...
Background: Informed consent is an ethical and legal requirement in healthcare and supports patient ...
Objective: Obtaining informed consent is a cornerstone requirement of conducting ethical research. T...
Objective: To systematically review audio-visual (AV) interventions for promoting informed consent (...
Background: As research involving human participants increasingly occurs with the aid of digital too...
BACKGROUND: Informed consent is one of the key elements in biomedical research. The introduction of ...
Background: As research involving human participants increasingly occurs with the aid of digital too...
Introduction Despite the 2015 Montgomery Ruling highlighting key requisites for informed consent, li...
Background Despite the 2015 Montgomery Ruling highlighting key requisites for informed consent, litt...
The bioethical principle of respect for persons re-quires that individuals participating in research...
BACKGROUND: Informed consent is a critical component of clinical research. Different methods of pres...
Informed consent is the cornerstone of human research subject protection. Many subjects sign consent...
Objective: The purpose of this study was to assess patient perceptions of using an interactive el...
Purpose: This study identifies best practices for informed consent for emergent computed tomography ...
Objective: To assess the efficacy, with respect to participant understanding of information, of a co...
To pursue scientific goals with patient data usually requires informed consent from the data subject...
Background: Informed consent is an ethical and legal requirement in healthcare and supports patient ...
Objective: Obtaining informed consent is a cornerstone requirement of conducting ethical research. T...
Objective: To systematically review audio-visual (AV) interventions for promoting informed consent (...
Background: As research involving human participants increasingly occurs with the aid of digital too...
BACKGROUND: Informed consent is one of the key elements in biomedical research. The introduction of ...
Background: As research involving human participants increasingly occurs with the aid of digital too...
Introduction Despite the 2015 Montgomery Ruling highlighting key requisites for informed consent, li...
Background Despite the 2015 Montgomery Ruling highlighting key requisites for informed consent, litt...
The bioethical principle of respect for persons re-quires that individuals participating in research...
BACKGROUND: Informed consent is a critical component of clinical research. Different methods of pres...
Informed consent is the cornerstone of human research subject protection. Many subjects sign consent...
Objective: The purpose of this study was to assess patient perceptions of using an interactive el...
Purpose: This study identifies best practices for informed consent for emergent computed tomography ...
Objective: To assess the efficacy, with respect to participant understanding of information, of a co...
To pursue scientific goals with patient data usually requires informed consent from the data subject...