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Related Concept Videos

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.
Nurses' Legal Responsibilities I01:27

Nurses' Legal Responsibilities I

In healthcare, informed consent is a crucial process that involves thoroughly communicating medical treatment options to patients, including benefits, risks, potential side effects, and alternatives. This process enables patients to make well-informed decisions about their care, ensuring they understand the implications of their choices before consenting to or refusing treatment.
The legal responsibilities of a nurse regarding informed consent include the following:
Bioavailability Study Design: Healthy Subjects Versus Patients01:15

Bioavailability Study Design: Healthy Subjects Versus Patients

Bioavailability studies are essential for evaluating a drug's therapeutic efficacy and understanding its absorption patterns under various physiological conditions. Conducting such studies on target patient populations provides more relevant data by simulating real-world disease states. However, practical challenges often necessitate the use of young, healthy adult volunteers as study subjects.Patients may exhibit altered drug absorption patterns due to the effects of the disease itself,...
Psychosurgery01:30

Psychosurgery

Psychosurgery, the surgical alteration or permanent removal of brain tissue to alleviate severe psychological conditions, stands as one of the most radical and controversial treatments in the history of mental health care. Its development and application have evolved significantly, marked by dramatic shifts in scientific understanding and ethical perspectives.
Historical Development of Psychosurgery
In the 1930s, Portuguese neurologist Antonio Egas Moniz introduced a surgical procedure designed...
Blind Procedures02:07

Blind Procedures

Ideally, the people who observe and record the children’s behavior are unaware of who was assigned to the experimental or control group, in order to control for experimenter bias. Experimenter bias refers to the possibility that a researcher’s expectations might skew the results of the study. Remember, conducting an experiment requires a lot of planning, and the people involved in the research project have a vested interest in supporting their hypotheses. If the observers knew which child was...
Blinding01:11

Blinding

Blinding is a commonly used method of not telling participants which treatment a subject is receiving. Blinding is a critical part of a randomized control trial or RCT. It reduces the bias that affects the results. In an RCT, blinding is used in the form of a placebo. A placebo effect occurs when untreated subjects falsely believe they have received the treatment and report improved symptoms. A placebo or a dummy treatment is administered to subjects to negate the bias caused by such an effect.

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Working with Human Tissues for Translational Cancer Research
07:48

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Published on: November 26, 2015

Informed consent and assent in human subject research.

G L Johnson1, R M Nelson

  • 1Medical College of Wisconsin, Milwoaukee, USA.

Journal of Public Health Management and Practice : JPHMP
|November 21, 2007
PubMed
Summary

Informed consent in human subject research ensures autonomy and respect for persons. Key elements include information, comprehension, and voluntariness, with considerations for child assent and public health research.

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Area of Science:

  • Biomedical and Behavioral Research Ethics
  • Public Health Research

Background:

  • Informed consent is crucial for upholding autonomy and respect for persons in human subject research.
  • Ethical guidelines emphasize three core elements: information, comprehension, and voluntariness.

Purpose of the Study:

  • To discuss the fundamental elements of informed consent in research.
  • To explore the concept of child assent.
  • To examine the application of informed consent in public health research.

Main Methods:

  • Literature review and ethical principle analysis.
  • Discussion of established ethical frameworks for human subject research.
  • Exploration of specific applications in child and public health contexts.

Main Results:

  • Informed consent requires providing adequate information, ensuring participant comprehension, and guaranteeing voluntariness.
  • Child assent is a distinct but related ethical consideration.
  • Public health research presents unique challenges and considerations for informed consent.

Conclusions:

  • Adherence to the principles of information, comprehension, and voluntariness is essential for ethical informed consent.
  • Child assent and specific public health research contexts require tailored approaches to informed consent.