Should Children Be Enrolled in Clinical Research in Conflict Zones?

Dónal O'Mathúna1, Nawaraj Upadhaya2

  • 1Associate professor in the College of Nursing and the Center for Bioethics and Medical Humanities at Ohio State University in Columbus.

AMA Journal of Ethics
|June 17, 2022
PubMed

Insights

Conducting research with children in conflict zones presents ethical challenges, including resource allocation and consent. Simultaneous research and clinical care are possible through community engagement to address these issues.

Area of Science:

  • Medical ethics
  • Global health research
  • Pediatric research

Background:

  • Ethical considerations for research in high-risk environments are complex.
  • Children in conflict zones face unique vulnerabilities.
  • Balancing clinical care with research demands is a critical challenge.

Observation:

  • Four key ethical issues identified: resource allocation, informed consent for minors, research feasibility, and maintaining neutrality.
  • Challenges in obtaining consent due to parental/guardian separation.
  • Ethical concerns regarding research feasibility and completion rates.
  • The imperative to maintain neutrality, impartiality, and humanity in research.

Findings:

  • Simultaneous clinical care and research are proposed as a viable approach.
  • Humble engagement with communities during all research phases is crucial.
  • Proactive community engagement can help resolve ethical dilemmas.

Implications:

  • This approach can improve ethical research conduct in conflict zones.
  • It highlights the importance of community-centered research methodologies.
  • Findings offer guidance for clinicians and researchers working with vulnerable pediatric populations in crisis settings.

Related Concept Videos

Clinical Trials01:16

Clinical Trials

Clinical trials are prospective experimental studies conducted on humans to determine the safety and efficacy of treatments, drugs, diet methods, and medical devices. Using statistics in clinical trials enables researchers to derive reasonable and accurate conclusions from the collected data, allowing them to make wise decisions in uncertain situations. In medical research, statistical methods are crucial for preventing errors and bias.
There are four phases in a clinical trial. A phase one...
7.4K
Ethics in Research01:56

Ethics in Research

Today, scientists agree that good research is ethical in nature and is guided by a basic respect for human dignity and safety. However, this has not always been the case. Modern researchers must demonstrate that the research they perform is ethically sound.
23.9K
Clinical Trials: Overview01:11

Clinical Trials: Overview

Clinical development focuses on how the drug will interact with the human body and encompasses four key phases of clinical trials, each serving a specific purpose in assessing the safety and effectiveness of new drugs. These phases overlap and build upon one another. Phase I involves a small group of healthy volunteers (typically 20-80 individuals) or, in cases where significant toxicity is expected, patients with the targeted disease, such as cancer or AIDS. The volunteers are tested for...
3.4K
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches01:23

Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches

Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
173
Study Designs in Epidemiology01:20

Study Designs in Epidemiology

Epidemiological study designs are fundamental tools for investigating the distribution, determinants, and control of health conditions in populations. They help researchers understand the relationships between exposures and outcomes, and they broadly fall into two categories: "observational" and "experimental" studies.
Observational studies are those where the researcher does not intervene but rather observes natural variations. They include cross-sectional, cohort, and...
407