Training Program Title

Challenges in Consenting Pregnant Women, Children and Neonates

Contributor

Tufts CTSI

CTSA Hub Administered

yes

Training Program Description

Consenting vulnerable populations

Competency Keywords

Study design, Clinical research, Clinical trial, Informed consent, Vulnerable population, Ethics, Drug, Regulatory guidelines, Clinicaltrials.gov

Digital Commons Disciplines

Medical Education | Medicine and Health Sciences

Public

yes

Cost to Access

no

Competency Domains

Scientific Concepts and Research Design; Ethical and Participant Safety Considerations; Clinical Trials Operations

Learning Objectives

-Identify important issues when conducting research on vulnerable populations
-Explain the challenges when consenting pregnant women or their infants
-Discuss the unique challenges of conducting research on premature infants (e.g., blood sampling, outcomes)

Delivery Method

In-person

Target Learners

Principal Investigators; Clinical Research Professionals (other than PI)

Learning Level

Advanced

Onboarding

no

Frequency

On demand

Time Needed

Half hour

Associated Assessment

no

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