Sentences with phrase «outcomes data collected»

In addition, we investigate the possible lagged effect of the interventions, based on outcomes data collected the year after the PD interventions concluded.

Outcome data collected by the research assistants who also acted as lactation educators and were not blinded.

For the study, researchers analyzed birthing outcome data collected from 2004 through 2009 by the Midwives Alliance of North America Statistics Project, commonly referred to as MANA Stats.

Outcome data collected at multiple time points over 12 months demonstrated that adolescents in the HIV intervention were less likely to report sexual intercourse, multiple partners, days of unprotected intercourse, and unprotected intercourse than those in the control group (Villarruel, Jemmott, Jemmott, & Eakin, 2006).

Not exact matches

More likely than not, you're already collecting this data, so make sure you're using it to your advantage by identifying correlations between which activities lead to certain sales outcomes.

Had it been made earlier, Facebook's decision to stop using third - party data providers for targeting would not have impacted the outcome of the Cambridge Analytica scandal, in which the outside firm collected the personal data of some 50 million Facebook users without their permission.

The only job involving numbers where you already know the outcome you want and just collect enough data to support your curve with the occasional outliers.

This work is resource intensive and it's important to collect good quality data, in order to identify positive outcomes and benefits, thus allowing a pragmatic argument to be made that the work is important.

Objective: To collect data from a cohort of women requesting a home birth and examine the experience and outcome of pregnancy, the indications for hospital transfer, and the attitudes of mothers, midwives, and general practitioners.

The aim of our study was to determine firstly, whether a retrospective linked data study was a viable alternative to such a design using routinely collected data in one Australian state and secondly, to report on the outcomes and interventions for women (and their babies) who planned to give birth in a hospital labour ward, birth centre or at home.

For the purposes of this economic evaluation, the forms were initially used in a related study funded by the National Institute of Health Research (NIHR) research for patient benefit programme «assessing the impact of a new birth centre on choice and outcome of maternity care in an inner city area,» which will be reported in full elsewhere, comparing the costs of care in a free standing midwifery unit with care in an obstetric unit in the same trust.16 The data collected included details of staffing levels, treatments, surgeries, diagnostic imaging tests, scans, drugs, and other resource inputs associated with each stage of the pathway through intrapartum and after birth care.

Data on additional risk factors or possible confounders, such as maternal age, parity, gestational age, ethnicity, and socioeconomic status, were collected from records accumulated during the pregnancy outcome study.

Given the heterogeneity in the choice of outcome measures routinely collected and reported in randomised evaluations of models of maternity care, a core (minimum) data set, such as that by Devane 2007, and a validated measure of maternal quality of life and well being would be useful not only within multi-centre trials and for comparisons between trials, but might also be a significant step in facilitating useful meta - analyses of similar studies.

The results of this study should be interpreted with caution because the breastfeeding team collected breastfeeding outcome data from the intervention group, thus introducing the potential for bias.

There are numerous prospective studies reporting the relation between breast feeding and respiratory morbidity (excluding allergic diathesis).27 — 35 The advantages of our study are that feeding data were collected before disease outcomes were known, hospital admission data were validated, and the study had ample statistical power.

In the intervention group outcome data were collected by the staff carrying out the intervention whereas in the control group outcome data were collected by a research interviewer who the women will not have met.

It was reported that outcome data were collected by blind investigators.

Outcome data were collected by a research assistant (by telephone).

Outcome data were collected at 4 months, but it is likely that there may have been recall bias for some outcomes, e.g. breast engorgement — women in the intervention groups would have discussed this and maybe it was recorded at the time it occurred, women in the control group would not have been asked until 4 months postpartum.

The research assistant collecting breastfeeding outcome data was not blinded with respect to treatment group.

The outcome data were collected by telephone at 6 months and by face - to - face interview in the home at 12 months.

In 66 of the 73 studies outcome data were collected from the women who had received the intervention.

Requiring universities and other research institutions to regularly collect, analyze, and disseminate data on career outcomes as a condition for receiving NIH funding, so that postdocs have a realistic idea about their prospects.

The NASEM report, commissioned by Congress in 2016, collected career aspiration, training, and outcome data from NIH, research institutions, and professional societies, as well as solicited suggestions from individual university administrators and biomedical scientists at different stages of their careers.The report especially zeroed in on the plight of the postdoctoral research fellow.

To develop the classifications, the nonprofit organization Rescuing Biomedical Research (RBR) convened a working group made up of trainee advocates and university administrators and career - development program directors who are involved in collecting career outcome data.

In Quebec, researchers established a patient registry in 2015 to collect demographic data on patients who use medical marijuana, the type and dose they take, and the conditions they're seeking treatment for, along with self - reports on benefits and adverse outcomes.

If, however, you are more interested in research you could become a health outcomes researcher, collecting data on therapeutic interventions for drug companies, or there is the Scientists Training Programme offered by the NHS.

For the new research, the scientists were able to tap databases from two well - known ongoing observational studies that collect data on diet and other lifestyle factors and various health outcomes.

Jon Davis and colleagues at the University of Cincinnati in Ohio collected outcome data on 80,000 people in the US who had had weight - loss surgery, including Roux - en - Y.

Participants report monarch larvae collection and rearing outcomes through a data portal, and those who collect parasitoid specimens are asked to wait until the flies hatch and then freeze them until sending them to the researchers.

Tilghman, Rockey, and the others in the working group laid out several recommendations aimed at shortening and diversifying doctoral programs and postdoc positions, increasing the proportion of trainees supported by training grants and fellowships instead of research grants, collecting more data on career outcomes, improving postdoc salaries, and promoting the staff scientist career path.

Scientists still have to analyze the data collected to learn more about how well the drug, called TKM - Ebola - Guinea, was tolerated and what specific effects it had on disease outcomes, says Peter Horby of the University of Oxford in the United Kingdom, who headed the study.

Data on anesthesia adverse events collected through the Anesthesia Quality Institute's (AQI) National Anesthesia Clinical Outcomes Registry (NACOR) are being presented at the ANESTHESIOLOGY ™ 2014 annual meeting.

Called Patient - Reported Outcome Measures, or «PROMs,» the data are collected using clinically - validated questionnaires that ask about symptoms, functional status, and quality of life.

Clinical Studies: Our clinical core, led by Dr. Kurt Christensen, conducts economic analyses alongside prospective clinical studies to better understand the full costs of sequencing and to collect real - world data about health care utilization and clinical outcomes following genomic tests.

«The MSPT is a potentially transformative approach to collecting MS disability outcome data for patient care and research,» explained Dr. Strober.

Opportunities lie ahead in the creation of strong partnerships with patients to collect post-approval, real - world data on treatment outcomes, and in the use of patient - led registries to both cut drug development costs and generate data on disease history / treatment outcomes.

The team will capture the tumor samples» genomic and transcriptomic data as well as the clinical outcomes and drug responses of each patient, starting with 842 participants and the already - collected tumor biopsies from 3,000 tumor regions among them.

But just before the final data on the last patient was collected in October, Lilly changed the outcomes so that the drug's success would rest solely on the cognitive changes, with the functional ones as a secondary measure of success.

The Foundation for Alternative and Integrative Medicine (FAIM) provides a service to the field by assisting researchers and practitioners in collecting clinical outcomes data.

Based on data from 5,604 psoriasis patients collected by the National Psoriasis Foundation (NPF), more than 52 percent of patients with psoriasis said that they were not happy with their conventional treatments, and 46 percent of psoriatic arthritis patients also commenting that they too were not happy with their outcomes from treatments.

Don't just collect the data and produce reports — take learning analytics to the next level by creating actionable outcomes from LA.

We collected college transcript data for all students in the sample, allowing us to examine the relationship between exam scores and several different outcomes, including grade point average (GPA) and enrollment in remedial courses.

The Scope of this project is to: - Provide seed funding and support pilot implementation of ideas resulting from the June 2014 design workshop on improving outcomes for babies in foster care; - Launch pilots of co-designed strategies for working collaboratively with parents in creating daily, regularized family routines in four sites and evaluate executive function skills, child development, child literacy and parental stress levels of participants pre -, during, and post-intervention; - Build a core group of leaders to help set the strategic direction for Frontiers of Innovation (FOI) and take on leadership for parts of the portfolio; - With Phil Fisher at the University of Oregon and Holly Schindler at the University of Washington develop a measurement and data collection framework and infrastructure in order to collect data from FOI - sponsored pilots and increase cross-site and cross-strategy learning; Organize Building Adult Capabilities Working Group to identify, measure and develop strategies related to executive function and emotional regulation for adults facing high levels of adversity and produce summary report in the fall of 2014 that reviews the knowledge base in this area and implications for intervention, including approaches that impact two generations.

Use the data collected to create graphs that link to curriculum outcomes.

Yet those same rubrics don't collect much in the way of «hard data» that demonstrate a candidate's prior effectiveness in improving student outcomes.

Federal and state officials collect data about the characteristics of students with disabilities and certain outcomes for those students, but little is known about the quality of education they receive, according to a report from the Editorial Projects in Education Research Center.

In joining a network, an agency would agree to pool its data, collect common outcomes such as a common interim assessment or teacher surveys, and work with the network organizer to establish a comparison group for each major intervention it implements.

In addressing the point of contention, the Productivity Commission is of the opinion that «there is little evidence or systematic processes in place to evaluate policies, program and teaching practices to identify what works best in schools and early learning centres», despite the amount of data that is collected to monitor and report on student and school outcomes.

There have been improved outcomes for students in relation to the accuracy of the data collected and the significant benefit of analysing this data to draw appropriate conclusions.