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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...
Data Collection by Experiments01:13

Data Collection by Experiments

Data collection is a systematic method of obtaining, observing, measuring, and analyzing accurate information. An experimental study is a standard method of data collection that involves the manipulation of the samples by applying some form of treatment prior to data collection. It refers to manipulating one variable to determine its changes on another variable. The sample subjected to treatment is known as “experimental units.”
An example of the experimental method is a public clinical trial...
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...
Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
Sampling Plans01:23

Sampling Plans

Sampling is a crucial step in analytical chemistry, allowing researchers to collect representative data from a large population. Common sampling methods include random, judgmental, systematic, stratified, and cluster sampling.
Random sampling is a method where each member of the population has an equal chance of being selected for the sample. It involves selecting individuals randomly, often using random number generators or lottery-type methods. For example, when analyzing the properties of a...
Group Design02:01

Group Design

The most basic experimental design involves two groups: the experimental group and the control group. The two groups are designed to be the same except for one difference— experimental manipulation. The experimental group gets the experimental manipulation—that is, the treatment or variable being tested—and the control group does not. Since experimental manipulation is the only difference between the experimental and control groups, we can be sure that any differences between the two are due to...

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A Clinical Trial Assessing the Safety, Efficacy, and Delivery of Olive-Oil-Based Three-Chamber Bags for Parenteral Nutrition
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Can treatment trial samples be representative?

Jackie A Wales1, Robert L Palmer, Christopher G Fairburn

  • 1University Department of Health Sciences, Brandon Unit, Leicester General Hospital, Leicester, UK. jw127@le.ac.uk

Behaviour Research and Therapy
|August 4, 2009
PubMed
Summary
This summary is machine-generated.

Eating disorder treatment trials can yield representative samples. Patients in trials mirrored those in regular clinics, suggesting findings are broadly applicable to similar settings.

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Area of Science:

  • Clinical Psychology
  • Psychiatry
  • Eating Disorder Research

Background:

  • Eating disorder treatment trials often use specific inclusion/exclusion criteria.
  • Concerns exist regarding the generalizability of trial findings to broader patient populations.
  • Representativeness of research samples is crucial for clinical applicability.

Purpose of the Study:

  • To assess the representativeness of a patient sample recruited for an eating disorder treatment trial.
  • To compare trial participants with patients from the same catchment area treated outside of a trial.
  • To determine the extent to which trial results can be generalized to typical clinical settings.

Main Methods:

  • A catchment area-based sample of eating disorder patients in a treatment trial was identified.
  • This sample was compared to patients from the same geographical area seen 12 months prior and post-trial.
  • Demographic and clinical characteristics of the three patient groups were analyzed.

Main Results:

  • The three patient samples (trial, pre-trial, post-trial) exhibited significant similarities.
  • The research sample was found to be representative of the usual clinic population.
  • This suggests minimal bias introduced by trial recruitment criteria.

Conclusions:

  • Eating disorder treatment trial samples can be representative of the general clinical population.
  • Appropriate study design and criteria allow for useful generalizability of trial findings.
  • Results from this trial can be extrapolated with confidence to similar clinical environments.