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Related Concept Videos

Data Collection II01:29

Data Collection II

9.8K
The nursing history captures and records the patient's health status, so that a care plan evolves to meet the patient's individual needs. The nursing health history is a part of the initial assessment. A comprehensive history covers all health dimensions and plays a significant role in the assessment process. A comprehensive history includes the patient's biographical information, reasons for seeking health care, expectations, present and past health history, medications, and...
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Data Collection I01:30

Data Collection I

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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...
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Data Collection by Experiments01:13

Data Collection by Experiments

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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...
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Data Collection by Survey01:07

Data Collection by Survey

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The systematic method of obtaining and analyzing accurate information of a population is called data collection. A survey is a standard method of data collection that involves collecting information from a target human population about their experience, opinion, or knowledge of a product, service, or process. The responses are recorded and interpreted. The most common survey examples are written questionnaires, face-to-face or telephonic conversations, focus groups, and electronic (e-mail or...
8.9K
Data Collection III01:05

Data Collection III

4.1K
The physical assessment examines the patient for objective data that defines the patient's condition, and aids in formulating the nursing care plan. The purpose of physical assessment is a health status appraisal, which includes identifying health problems, and establishing a database for nursing intervention.
The principles to begin the physical assessment include conducting a comprehensive or problem-related history in a quiet, well-lit room, emphasizing privacy and comfort for the...
4.1K
Data Collection by Observations01:08

Data Collection by Observations

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Data collection refers to a systematic way of obtaining, observing, measuring, and analyzing accurate information. Observational studies are one of the most widely used methods of data collection. It involves collecting data by observing the behavior and physical characteristics of a sample without making any modifications to the sample.
An astronomer viewing the motion and brightness of stars in the sky and recording the data is an example of observational data collection. A botanist recording...
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Updated: Jan 27, 2026

Optimization of Breast Biopsy and Mastectomy Sample Collection Procedures for Biobanking, Personalized Medicine, and Research Applications
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A Two-Level Biobank Data Protection Concept for Project-Driven Human Sample Collections.

Antje Müller1, Jan Hovanec1, Berthold Josephs1

  • 1Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr University Bochum (IPA), Bochum, Germany.

Biopreservation and Biobanking
|March 19, 2019
PubMed
Summary
This summary is machine-generated.

Human biobanks face challenges in protecting donor privacy while enabling research. This study presents a transferable data protection concept for biobanks, balancing participant privacy with biomaterial and data accessibility for future studies.

Keywords:
biobankingbiorepositorydata managementethicslegal requirementsprivacy

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Area of Science:

  • Biobanking
  • Data Protection
  • Research Ethics

Background:

  • Increasing legal and ethical demands for enhanced research participant privacy in human biobanks.
  • Growing need for robust data protection schemes to minimize donor reidentification risk.
  • Lack of publications addressing foundational data protection strategies for biobanks.

Purpose of the Study:

  • To present a data protection concept for a project-driven, stand-alone human biobank.
  • To address simultaneous needs of primary research project support and long-term biomaterial provision.
  • To offer a transparent and basic framework for biobank data protection.

Main Methods:

  • Developing a data protection concept based on national and international laws and ethical guidelines.
  • Integrating data protection measures into both primary research project operations and long-term biobank provisions.
  • Focusing on transparency and basic, transferable measures.

Main Results:

  • A comprehensive data protection concept designed for a stand-alone biobank.
  • Simultaneous management of data for primary research and future biomaterial use.
  • Measures are transparent, basic, and adaptable to various legal contexts.

Conclusions:

  • The presented data protection concept effectively balances research participant privacy with data accessibility.
  • The transparent and basic nature of the concept facilitates its adoption and adaptation by other biobanks.
  • This framework supports the responsible and sustainable operation of human biobanks.