Sentences with phrase «participant data research»

Not exact matches

Facebook's AI research team has created a free software toolkit that outsiders can download to help with their experiments by compiling data and viewing the research and results of other participants in the project.

Here's how The British Psychological Society Research Digest blog sums up the results: «The data showed that the more a participant had turned their thoughts towards what they had in common with the other director, the more their ingratiation behaviors paid off — they were more likely to get an invitation to join the board in the months that followed.»

It is expected the research and analysis around this data will provide the foundation for a number of leading conferences and high level industry roundtables to identify and promote appropriate market structures for the benefit of all participants.

One of the participants at the research conference, an electronic church broadcaster, summed up all of the data by stating, «It looks like the research is saying that all that religious TV is doing is to make people feel good and to get them to keep on doing what they're doing!»

To prevent the exploitation or coercion of research participants, universities and other organizations conducting or sponsoring research require that all researchers who intend to use data collected from human subjects be familiar with national and state - level guidelines for working with human subjects data.

Initially, open questions were used to pursue research themes, which were then followed up using the participants» own words and phrases as a means of eliciting further data (Hollway and Jefferson, 1997).

These new governance structures must be able to address the concerns of research participants while at the same time ensuring effective data sharing that promotes public trust in genomics research.

Next - generation sequencing and global data sharing challenge many of the governance mechanisms currently in place to protect the privacy of research participants.

Using data from a nationally representative sample of youth who participated in the National Health and Nutrition Examination Survey (NHANES), a group of researchers led by Dr. Kathleen Merikangas of the National Institute of Health Intramural Research Program, evaluated symptoms of ADHD and its subtypes in 1,894 participants aged 12 - 15 years based on parent reports of symptomatology.

He said because extreme sports participants found it hard to put their experiences into words, the research project had taken a new approach to understanding the data.

Data used for the study came from research participants who were granted anonymity.

The top three general responsibilities for supervising postdocs identified by survey participants were discussing research project and direction (96 percent), reviewing data analysis and interpretation of results (91 percent), and assisting with writing manuscripts and seminar preparation (84 percent).

The research team explored data from more than 100,000 participants in the Nurses» Health Study (NHS), looking at rates of cardiovascular disease, specifically incidence of coronary heart disease and stroke.

The ARIC data were especially useful to study because unlike most previous research linking gum disease and cancer risk, periodontitis cases were determined from dental examinations performed as part of the ARIC study rather than participants» self - reports of the disease.

The new study, funded by the National Institute for Health Research, and published in The Lancet Respiratory Medicine, collated and analysed the individual data from 955 participants in seven randomised controlled trials, which tested the use of vitamin D supplements.

In addition, the research team analyzed data based on participants» smoking rate and level of nicotine dependence.

For this population - based research, investigators pooled data from large cohort studies conducted in Asia and included demographic and risk factor information collected in seven Asian regions from the early 1960s through the late 1990s (although most of the studies enrolled participants after the mid-1980s).

In order to investigate whether a healthy lifestyle can mitigate genetic risk, the multi-institutional research team analyzed genetic and clinical data from more than 55,000 participants in four large - scale studies.

Democrats vehemently objected to the subpoena, however, arguing that making the raw data public would violate confidentiality agreements with study participants and subject the research to attack from representatives of polluting industries.

Investigators are encouraged to seek the broadest possible sharing permissions from participants for future research use of their data.

Timelines for data submission and access should promote timely and broad data sharing while being mindful of the significant effort by investigators to generate and prepare data for release, as well as to realize benefit from engaging research participants.

The National Institutes of Health has issued a final NIH Genomic Data Sharing (GDS) policy to promote data sharing as a way to speed the translation of data into knowledge, products and procedures that improve health while protecting the privacy of research participaData Sharing (GDS) policy to promote data sharing as a way to speed the translation of data into knowledge, products and procedures that improve health while protecting the privacy of research participadata sharing as a way to speed the translation of data into knowledge, products and procedures that improve health while protecting the privacy of research participadata into knowledge, products and procedures that improve health while protecting the privacy of research participants.

Access to other data has been controlled and made available only for research purposes consistent with the consent provided by participants in the original study.

A key tenet of the GDS policy is the expectation that researchers obtain the informed consent of study participants for the potential future use of their de-identified data for research and for broad sharing.

Subject areas, such as genetic discrimination, patient (and research participant) right to privacy, and ownership of genetic material and data, showed both the negative ways scientific information can be used and some of the gray areas that confront researchers every day.

Salil Vadhan, a professor of computer science at Harvard University and former director of the Center of Research on Computation and Society, is among the researchers exploring an approach known as «differential privacy» that allows one to investigate data without revealing confidential information about participants.

In addition to consenting to an IRB - approved trial in the first place, participants must also give consent for 23andMe to share their personal data with the research study, and may also consent to contributing anonymized data to 23andMe's proprietary database.

Angela serves as the Participant Coordinator for the Health Outreach Program for the Elderly (HOPE) study, a research registry that is collecting longitudinal data on approximately 600 older adults with or without memory problems.

The workshop participants (approximately 40 scientist from 10 countries) are in the process of producing a Guide to Best Practices for Ocean Acidification Research and Data Reporting.

The Registry has helped recruit participants and provide data for clinical trials and other important SMA research studies.

The data which are identifiable, including name and NHS number, will be seen only by a University of Leeds employee who will link the data provided by NHS Digital to the data collected directly from each participant by the research group.

The Registry has helped recruit participants for clinical trials and has provided data for important SMA research studies.

Data that is anonymised / pseudonymised better protects research participants» privacy and is not subject to the same restrictions as Personal Data.

MoBagenetics is a research infrastructure aiming to genotype all participants in MoBa, and offer access to this data using a secure analysis platform to approved research projects.

Much of the research at the Sanger Institute requires collection of data from research participants.

Researchers should be aware that the Data Protection Act also covers recordings and images of patients and research participants where these contain, or are held with, identifying information.

Study co-author Dr. Sukhbinder Kumar, research fellow at the Institute of Neuroscience at Newcastle University, and a team of scientists evaluated the data of 42 participants (20 with misophonia, 22 without).

After completing the course, the participant will be able to determine what is appropriate microscopic technique used to answer the research questions, including the preparation and data processing for publication.

The new research included data from two prior long - term studies, which collectively had more than 170,000 total participants.

Resources include 10 - 12 lessons covering introduction to research methods, reliability and validity, sampling and questionnaires, experiments, the research process, focus groups and interviews, participant and non-participant observation, secondary data, longitudinal and case studies plus research methods revision bundle.

Expanded data and research about MOOC participants and evidence - based assessments of online learning trends might, however, begin to move the conversation beyond anecdotes and heated opinions.

The participants were all from ACT Catholic schools and they recommend further research is carried out using student data from other jurisdictions and across sectors.

In a project called CoVis, for example, participants learn about science using some of the same research tools and data sets used by scientists in the field.

The handbook is organized according to how program inputs and outcomes have been conceptualized and validated in evaluation research on leadership preparation programs and will help program designers: 1) Identify Formative and Summative Assessments; 2) Identify Measures and Outcomes (e.g., program and participant outcomes); 3) Evaluate the Relationship Between the Program Attribute and the Outcome; and 4) Use Data for Preparation Program Improvement.

In addition, NCES periodically offers seminars to stimulate interest in using NAEP data to address educational research questions, enhance participants» understanding of the methodological and technological issues relevant to NAEP, and demonstrate the steps necessary for conducting accurate statistical analyses of NAEP data.

It also examines feedback from program participants and relevant data and research about programs.

Our research examined participants» views of their own learning and professional growth, drawing primarily on analysis of interview data and personal writing done by the teachers as part of course and club participation.

Participants have access to CORE's multimetric school and district data dashboards in addition to their analytical and research partners.

Teachers» Intellectual Identity in the Study Group Experience Our research on the study group examined participants» views of their own learning and professional growth, drawing primarily on analysis of interview data and personal writing done by the teachers as part of course and club participation.

The proposed retention is for permanent status for the research data collected via on - board computer and through participant questionnaire responses, as these data have value in future research.