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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...
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...
Nursing Clinical Information System01:27

Nursing Clinical Information System

Nursing Clinical Information System (NCIS)
A Nursing Clinical Information System (NCIS) is a specialized type of healthcare information system tailored to meet the unique needs of nursing practice. It incorporates the principles of nursing informatics to streamline information management and improve the quality of care delivery.
Critical attributes of NCIS include:
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, controlled...
Data Collection I01:30

Data Collection I

Data collection gathers information needed to make accurate judgments about a patient's present condition. During a health history interview, subjective data is collected from the patient, their caregivers, or family members, and objective data is collected through observations and physical assessment. Patients are the primary source of subjective data. Thus information gathered from patients through interviews, observations, and physical examination is primary data. Secondary sources of data...
Archival Research01:40

Archival Research

Some researchers gain access to large amounts of data without interacting with a single research participant. Instead, they use existing records to answer various research questions. This type of research approach is known as archival research. Archival research relies on looking at past records or data sets to look for interesting patterns or relationships. For example, a researcher might access the academic records of all individuals who enrolled in college within the past ten years and...

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Related Experiment Video

Updated: Jun 21, 2026

TBase - an Integrated Electronic Health Record and Research Database for Kidney Transplant Recipients
09:00

TBase - an Integrated Electronic Health Record and Research Database for Kidney Transplant Recipients

Published on: April 13, 2021

The research database in clinical practice.

P S Jensen

    Journal of Child and Adolescent Psychopharmacology
    |July 28, 2009
    PubMed
    Summary
    This summary is machine-generated.

    Implementing systematic methods for patient evaluation in clinical care can create research databases. These databases aid in studying clinical questions and integrating research with practice, despite potential challenges.

    Related Experiment Videos

    Last Updated: Jun 21, 2026

    TBase - an Integrated Electronic Health Record and Research Database for Kidney Transplant Recipients
    09:00

    TBase - an Integrated Electronic Health Record and Research Database for Kidney Transplant Recipients

    Published on: April 13, 2021

    Area of Science:

    • Clinical Research
    • Health Informatics
    • Medical Practice Management

    Background:

    • Systematic patient evaluation and monitoring are crucial in routine clinical care.
    • Integrating research within clinical settings presents unique practical, scientific, and clinical challenges.
    • Clinical research databases offer a potential solution for studying clinical questions efficiently.

    Purpose of the Study:

    • To explore the utility of clinical research databases in routine patient care.
    • To identify key considerations for developing and implementing clinical research databases.
    • To examine the benefits and limitations of using clinical databases in practice.

    Main Methods:

    • The abstract discusses the conceptual framework and considerations for establishing clinical research databases.
    • It highlights the importance of systematic data collection and patient monitoring.
    • It addresses potential pitfalls such as data redundancy and statistical biases.

    Main Results:

    • Clinical research databases can be valuable tools for addressing clinical questions.
    • Careful planning is required to mitigate challenges like data overload and misinterpretation.
    • Despite limitations, these databases can support hypothesis testing and improve patient care.

    Conclusions:

    • Clinical research databases facilitate the integration of research and clinical practice.
    • Addressing practical and statistical issues is essential for effective database utilization.
    • These databases can enhance the quality of care and support evidence-based psychopharmacology.