Sentences with phrase «clinical research participants»

Not exact matches

Former Time Warner CEO & MM patient shares importance of patients being active participants in clinical research Read More

Participants included CEOs Jonathan Bush of Athenahealth, Ron Gutman of HealthTap, Dr. Clifford Hudis of the American Society of Clinical Oncology, Dr. Vivian Lee of University of Utah Health Care, VitalConnect CEO Nersi Nazari, James Park of Fitbit, and Andrew Witty of GSK, as well as President of Flex Health Solutions John Carlson, Multiple Myeloma Research Foundation Founder Kathy Giusti, Dr. Sanjay Gupta, Arianna Huffington, Andreessen Horowitz General Partner Vijay Pande, Parker Foundation President Sean Parker, Women's Alzheimer's Movement Founder Maria Shriver, and White House Cancer Moonshot Task Force Executive Director Greg Simon.

All study participants gave written informed consent and the study was approved by the Monash University Human Research Ethics Committee (approval number CF12 / 0348 -2012000146), and the trial registered with the Australia and New Zealand Clinical Trial Registry (registration number 12611000468921).

In addition to clinicians, consumers, health professional educators, insurers, lawyers, ethicists, administrators, and policy makers, the participants included researchers with expertise in epidemiology, public health, sociology, medical anthropology, legal, health policy and clinical research.

«We have now found a potential mechanism, and at this point in our research, we need to test human participants in a blinded, placebo controlled clinical study — the same technique we used to study the behavioral effects of acupuncture in rats,» says Eshkevari, a nurse anesthetist and licensed acupuncturist.

The participants in the Starbrite trial bring considerable clinical and research experience.

For instance, clinical trial participants can avoid the inconvenience of visiting research facilities, writing down their daily activities or wearing clunky monitors.

In that older approach, trial participants worked iteratively and explicitly through target acquisition attempts while a trained clinical research technician monitored and updated the software.

¬ In all of Griffiths» clinical research, people given psilocybin are provided a safe, comfortable space with trained experts to offer support to participants.

A drug used to treat men with late - stage prostate cancer proved effective in stemming progression of the disease in research participants who had not yet received chemotherapy and extended their survival, according to results from a multi-national Phase III clinical trial led by the Knight Cancer Institute at Oregon Health & Science University (OHSU).

Finally, the research team tested a drug already in clinical trials (IGF - 1) on a cohort of study participants, finding that it provoked a reversal of neural alterations, though the degree of response varied by ASD individual.

«With continued clinical research, we will learn how our findings extend to more participants.

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.

Participants are recruited from retirement communities and subsidized housing facilities in and around Chicago to participate in annual clinical evaluations and magnetic resonance imaging (MRI) scans, and to donate their brains and other parts of their bodies for research after their deaths.

«This program capitalizes on local resources that can bring about change in behavior and improve blood pressure rates,» said Monique Anderson, M.D., lead researcher of the study and a medical instructor in cardiology at the Duke Clinical Research Institute and the Duke School of Medicine in Durham, N.C. «As participants became more knowledgeable, they probably started exercising more, taking their medication more, and those who were really engaged showed dramatic responses in blood pressure change.»

The clinical research center CAIMED, part of Ponce Health Sciences University in Puerto Rico, will examine the vaccine's safety and immunogenicity in participants who have already been naturally exposed to Zika or dengue viruses

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

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.

This paper describes results from a clinical trial that demonstrates that a single dose of a broadly neutralizing anti-HIV-1 monoclonal antibody is well tolerated and reduces viral load in a cohort of 33 research participants.

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

phenomenon whereby a research participant conflates the goals of research with those of clinical treatment) and ensure that all prospective trial participants have adequate post-trial access to treatment and DBS device maintenance.

The article by Mansukhani et al1 in this issue of JAMA Surgery reveals that, despite the introduction of the National Institutes of Health Revitalization Act of 1993 to ensure that female participants were included in clinical trials, males and females currently are not included in surgical clinical research in equal numbers.

But research published in the American Journal of Clinical Nutrition2 revealed that study participants taking relatively higher doses of supplemental iodine — 400 micrograms a day and more — paradoxically began developing subclinical hypothyroidism.

«Previous studies have explored these heart attack triggers; however, they had fewer participants or were completed in one country,» says lead author Andrew Smyth, MD, PhD, a researcher at McMaster University in Canada and at the HRB Clinical Research Facility in Ireland.

Participants were admitted to the Institute for Translational Science — Clinical Research Center (ITS - CRC) at ∼ 1500 h the day before each metabolic study.

Our mission is three-fold: to provide high - quality, developmentally - appropriate educational programs for children; to provide a clinical setting in which students preparing for careers working with young children can observe and participate in the application of theory into practice; and to facilitate educational research opportunities that engage participants in the process of investigation, reflection, and documentation.

Participants in this two - day on - campus program will work with renowned thought leaders, including Laurie M. Brotman, Bezos Family Foundation Professor of Early Childhood Development, Department of Population Health, and Professor, Department of Child and Adolescent Psychiatry, NYU School of Medicine; Lyrica Fils - Aime, Community School Director of Children's Aid and Director of Clinical Services and Training at OmPlay; Carla Shalaby, Postdoctoral Fellow with TeachingWorks at the University of Michigan and author of Troublemakers; and Amanda Williford, Research Associate Professor at the University of Virginia, and one of the creators of the innovative Banking Time program.

Qualifying fellowships may be tailored to particular student interests and are intended to introduce student participants to career opportunities in any aspect of the broad field of laboratory animal science, including clinical laboratory animal medicine (clinical service and administration, experimental surgery, or animal welfare and behavior); pathology (anatomic or clinical); or biomedical research involving laboratory animals.

The Code, however, did not directly address the ethical conduct of non-interventional research, such as medical records research, where the risk of harm to participants can be unlike those associated with clinical research.

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.

Facilitated clinical research efforts by serving as an intermediary for study participants, sponsors, outside consultants and colleagues.

Clinical Coordinators are involved with clinical trials and research projects and are responsible for managing programs, assigning tasks, recruiting and training participants, and networking with Clinical Coordinators are involved with clinical trials and research projects and are responsible for managing programs, assigning tasks, recruiting and training participants, and networking with clinical trials and research projects and are responsible for managing programs, assigning tasks, recruiting and training participants, and networking with clients.

Use Microsoft Access and Excel to enter data collected on study participants from the Computer - Assisted Personal Interview (CAPI) and abstract clinical information from their Electronic Medical Records (EMR) which is entered in Discovere, a web - based research platform used to manage and analyze study data.

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

Nurse Researcher Penn Medicine, Hampton, GA 10/2012 — Present • Provide and coordinate clinical care for patients involved in clinical research studies • Ascertain accuracy of data collection and data recording, and handle correlating follow - up • Schedule evaluation screenings and ensure that all participant are made physically and mentally ready for them • Provide patient participants with information on what to expect during clinical trials • Handle administration of investigational drugs, and handle detailed clinical assessments • Study chronic and acute diseases and disorders, and assist in developing new treatment plans • Assist in testing new treatments and medications that may change the way diseases and disorders are perceived • Compile clinical data and review and assess it for reporting purposes

I have experience in research and have been a participant in published clinical trials.

HIGHLIGHTS OF QUALIFICATIONS * Over 4 + years of progressive work experience in clinical and academic research hospital settings, collaborating with investigators and a multidisciplinary health care team in the recruitment of study participants for various investigator - initiated and industry sponsored clinical trial studies.

Confidentiality: Participant confidentiality is strictly held in trust by the investigators, research staff, and the sponsoring institutions and their agents, and is extended to cover clinical information relating to participants.

In addition to the general constraints of conducting research in an applied setting, program evaluations pose special obstacles for researchers because of the clinical and ethical issues involved in withholding treatment or wait - listing participants who clearly might benefit from the program (i.e., at - risk students, low - income families).

Level 1 Clinical Training will give participants new insights into treatment for couples who struggle, using research - based assessments and effective interventions based on the Sound Relationship House Theory.

Based on groundbreaking research by Kristin Neff and integrated with the clinical perspective of Christopher Germer, MSC teaches core principles and practices that enable participants to respond to difficult emotions with kindness and understanding.

Participants completed a self - administered computerized version of the Clinical Interview Schedule — Revised (CIS - R) 28 at the 18 - year research clinic (mean age 17 years, 10 months) conducted in 2009 to 2010.

Development and initial validation of the Therapeutic Misunderstanding Scale for use with clinical trials research participants.