Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Ethics in Research01:56

Ethics in Research

26.3K
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.
26.3K
Data Collection II01:29

Data Collection II

10.5K
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...
10.5K
Data Collection I01:30

Data Collection I

9.0K
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...
9.0K
Data Collection by Survey01:07

Data Collection by Survey

9.7K
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...
9.7K
Data Collection by Experiments01:13

Data Collection by Experiments

28.2K
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...
28.2K
Archival Research01:40

Archival Research

17.6K
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...
17.6K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

What are the arguments for and against recognizing 'terminal' anorexia nervosa? A narrative review.

International review of psychiatry (Abingdon, England)·2026
Same author

Redefining success and failure in community-engaged environmental health research.

Annals of the American Thoracic Society·2026
Same author

Ashley's Legacy: Supporting Caring Relationships Within Families.

The American journal of bioethics : AJOB·2026
Same author

Perceptions of health research participation in rural and urban Pennsylvanians.

Journal of clinical and translational science·2026
Same author

Bridging the gap: Community insights on effectively sharing research findings with the public.

Journal of clinical and translational science·2026
Same author

New treatments, novel conversations: A need to study the science of communication about treatment options for inborn errors of metabolism.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Related Experiment Video

Updated: Apr 16, 2026

Visualizing Field Data Collection Procedures of Exposure and Biomarker Assessments for the Household Air Pollution Intervention Network Trial in India
09:33

Visualizing Field Data Collection Procedures of Exposure and Biomarker Assessments for the Household Air Pollution Intervention Network Trial in India

Published on: December 23, 2022

3.1K

Building a Central Repository for Research Ethics Consultation Data: A Proposal for a Standard Data Collection Tool.

Mildred K Cho1, Holly Taylor2, Jennifer B McCormick3

  • 1Stanford University, Stanford, California, USA.

Clinical and Translational Science
|March 12, 2015
PubMed
Summary
This summary is machine-generated.

Clinical research ethics consultation services are improving through a standardized data collection approach. This framework supports quality improvement, education, and research, enhancing ethical research conduct across institutions.

Keywords:
FDAbiostatisticsconsultationethicsquality improvement

More Related Videos

Functional Near-Infrared Spectroscopy Hyperscanning Study in Psychological Counseling
06:04

Functional Near-Infrared Spectroscopy Hyperscanning Study in Psychological Counseling

Published on: January 17, 2025

1.8K
Working with Human Tissues for Translational Cancer Research
07:48

Working with Human Tissues for Translational Cancer Research

Published on: November 26, 2015

10.4K

Related Experiment Videos

Last Updated: Apr 16, 2026

Visualizing Field Data Collection Procedures of Exposure and Biomarker Assessments for the Household Air Pollution Intervention Network Trial in India
09:33

Visualizing Field Data Collection Procedures of Exposure and Biomarker Assessments for the Household Air Pollution Intervention Network Trial in India

Published on: December 23, 2022

3.1K
Functional Near-Infrared Spectroscopy Hyperscanning Study in Psychological Counseling
06:04

Functional Near-Infrared Spectroscopy Hyperscanning Study in Psychological Counseling

Published on: January 17, 2025

1.8K
Working with Human Tissues for Translational Cancer Research
07:48

Working with Human Tissues for Translational Cancer Research

Published on: November 26, 2015

10.4K

Area of Science:

  • Clinical Research Ethics
  • Health Services Research
  • Bioethics

Background:

  • Clinical research ethics consultation services have grown in academic health centers.
  • Standardized data collection is needed for quality improvement, education, and research.
  • Collaboration within the CTSA consortium is key to developing these standards.

Purpose of the Study:

  • To develop a standard approach for collecting clinical research ethics consultation information.
  • To establish a foundation for quality improvement, education, and research in clinical ethics consultation.
  • To explore challenges in sharing consultation data between institutions.

Main Methods:

  • Developed a categorization system for research ethics consultation data.
  • Defined descriptive information categories: requestor, project, ethical question, consult process, and consult note structure.
  • Explored data sharing challenges including confidentiality, data quality, and informatics.

Main Results:

  • A structured approach to documenting research ethics consultations was created.
  • Identified key data points for consultation services.
  • Highlighted challenges in inter-institutional data sharing.

Conclusions:

  • Standardized data collection tools can advance clinical research ethics consultation.
  • Improved consultation processes facilitate the ethical conduct of research.
  • Further work is needed to refine data sharing and utilization.