Sentences with phrase «subject research participants»

Not exact matches

PsyBlog explains the research on the subject: «In the study, one group of participants were allowed to get a full nights» sleep, while another had to stay up all night.

PsyBlog sums up one study on the subject which entailed showing some research participants a video on the idea that stress can be enhancing: «This led to them reporting better performance at work and fewer psychological problems over the subsequent two weeks.

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.

The research looked at more than five million genetic variations, called single nucleotide polymorphisms or SNPs (pronounced «snips»), in each participant in the study and compared the frequency of these SNPs with that of the control subjects.

The subject pool was more than 2,000 undergrads from multiple sections of an introductory psychology course who volunteered as research participants over the past few years.

The Obama Administration is exploring fundamental reforms to human subjects protections — actions that are being driven in part by the fact that technological advances, especially in genomics and computing, have made the notion of «de-identifying» a research participant's biological sample virtually impossible.

This means that the institution, whether a public university or a private sponsor, must establish a human research participant protection program (HRPPP) with multiple levels of responsibility and accountability, from the IRB (which, by federal law, prospectively reviews all federally funded human subjects research protocols) to the chief administrator (Chancellor or CEO) to the investigator, staff, and students, to the research participants.

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.

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.

Research subjects were given a tablet computer (pictured) that provided a continually updated display of their medication - taking activities, while the other half of study participants were given no additional feedback.

In this role, Ms. Roxland re-launched and chaired J&J's Ethics Committee, created an enterprise - wide consultation service for teams and individuals confronting complex research ethics issues, and provided guidance on issues such as post-trial access for former research participants, conducting clinical trials in war - torn regions, testing of a potential Ebola vaccine during a public health crisis, commercialization of stem cell therapies, subject recruitment and withdrawal, and expanded access / compassionate use.

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

In response to mounting concerns about the adequacy of protection of research participants, at a regulatory level, increasing attention is being focused on safety and confidentiality of human subjects participating in research protocols.26 - 28 Beginning with applications submitted for the January 2001 council round, institutional review board (IRB) approval is no longer required prior to NIH peer review; previous NIH policy had been that IRB approval was required at the time of submission.

Technical coordinator of a national convention in France involving industry and universities on the same subject Since 1992: Organizer of a cycle of international conferences on «Heavy scintillators for scientific and industrial applications» First one in Chamonix, France in 1992 (200 participants), 9th one in Winston Salem (NC, USA) in 2007 (300 participants) 1994 - 2007: As Technical coordinator of the CMS electromagnetic calorimeter at the LHC Large Hadron Collider, responsible for the technical development and the mass production of 76» 000 Lead Tungstate crystals (100 tons) 1994 - 2000: Organizer of the development and mass production organization of Lutetium Aluminum perovskite crystals, in particular for PET scanner applications Since 2000: Strong involvement in the development of dedicated breast imaging camera combining several modalities for a multiparametric evaluation of breast tumors (anatomic, structural and functional) Since 2002: Feasibility study and setting - up of an international medical imaging research centre, presently being built in Marseille (Cerimed)

Continuing the Conversation Lamb, the mother of two sons, aged 17 and 23, says she was fortunate to have live research subjects at home, even if they were not always willing participants — a problem I also encountered when my previously quoted nine - year - old saw his name, since removed, in this article.

As a Researcher in Schools participant I am able to keep my own research ongoing, keeping myself updated and nurturing my own passion for the subject.»

When I was presenting on this subject recently at the LSIS annual research conference one participant commented:

Live this transformative experience with an international group of participants, in a supportive and creative environment that seeks to experiment and push boundaries of researching and developing progressive interdisciplinary works, in relation to relevant socio - political and environmental subjects of our time.

One contract specifies that the issuer may use and disclose protected health information about the participants in the group health plan for research purposes without authorization (subject to the requirements of this rule) and one contract specifies that the issuer must always obtain authorizations for these uses and disclosures.

In fact, IRB review may be even more important for research conducted with subjects» informed consent and authorization since such research may present greater than minimal risk to participants.

Common duties of a Clinical Research Coordinator include: allocating budgets and resources, disclosing study aspects to participants, evaluating and analyzing study data, adhering to protocols and regulations, liaising with professional organizations, ordering supplies needed for study completion, handling specimens, developing informational materials, collaborating with healthcare professionals, and supervising subject enrollment.

Adept at assisting with the development and implementation of research programs, coordinating with clinical and subject participants, and collecting and organizing research data.

Each participant gave written informed consent in accordance with institutional Human Subjects Research Committee guidelines.

Both longitudinal studies were approved by the local ethical committee for research on human subjects (CMO) Arnhem - Nijmegen in The Netherlands, and informed consent was obtained from all participants.

Most research articles had both male and female participants (64 %); however, 33 % of articles had solely female subjects and 3 % solely male subjects.