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As an example, it was considered the European Lead-cooled System (ELSY) international project response under a reference design basis earthquake (Safe Shutdown Earthquake-SSE) excitation, taking into account also the main isolating device effects in order to increase the reactor safety.
The main targets of the project (response time, long-term stability and accuracy) were achieved.
This paper focuses on the assessment of AFR within the project REsponse to ACcountable priority setting for Trust in health systems (REACT).
In 2006, African researchers, in collaboration with colleagues from Europe, launched the five-year project: Response to Accountable Priority Setting for Trust in Health Systems REACTT).
The data originates from the ongoing EU funded research project "REsponse to ACountable Priority Setting for Trust in Health Systems" (REACT) implemented in the three countries which has a research component linked to HIV and testing, and from an additional study focusing on HIV testing, counselling perceptions and experiences in Kenya.
In the framework of the EU-funded project 'Response to Emerging infectious disease: Assessment and development of Core capacities and Tools' (REACT), we have investigated the available evidence and tools on contact tracing aiming to guide public health institutions in their decision-making.
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Having developed a priority list of concerns, appropriate project responses were developed over the next 12 15 months April 2004 July 2005005) in partnership with the Community Advisory Committee (CAC) through discussion at site-level meetings.
The interviewer assigned to conduct the diagnostic interview will call back 50 times or more if necessary to obtain the projected response rate within the field period.
The sample size calculations are based on (1) published descriptive statistics for hair nicotine and hair cotinine, (2) specified effect sizes, (3) a projected average clinic size of 30 infants, and (4) a projected response rate of 80%.
To estimate a projected response of 65% [based on CDC minimum weighted response rates] with a lower confidence limit of 60% and upper confidence limit of 75% we sampled 124 women to the study.
This component of the design is based on the parameters p0, the estimated response rate to an "ineffective novel therapy", and p1, the projected response rate to an "effective novel therapy" that we would like to evaluate in a RCT.
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