Sentences with phrase «clinical research study participants»

Not exact matches

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).

«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.

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.

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.

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

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

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.

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.

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.

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

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.