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The objectives of this paper are to describe the research activities associated with CBCS-HCV development and pilot testing, including: (1) formative work leading to intervention development; (2) preliminary study protocol; and (3) pilot feasibility testing of the intervention and study design.
The primary analysis will compare mortality at 18 months between the intervention and control arms, while taking into account the design-based cluster matching and the testing of the intervention effect over all community pairs.
In this paper, development and initial testing of the intervention, is discussed.
AF was responsible for reviewing the results from previous research and pilot testing of the intervention.
Twenty-one women with GDM, from multi-ethnic backgrounds, participated in the testing of the intervention.
Finally, Phase II field testing of the intervention was carried out.
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The consequence of any contamination would be to attenuate the intervention effect, such that the trial would be a conservative test of the intervention.
A post hoc test of the intervention × time interaction revealed that in the MSG sessions (P < 0.040) but not in placebo sessions (P > 0.900), sBP was elevated 15 and 30 min after intake (Figure 5). Figure 5 The time course of changes in mean (± SEM) systolic and diastolic blood pressure during monosodium glutamate (MSG) and placebo intervention.
The development and pilot-testing of the intervention will be reported separately in detail.
It is possible that our study does not represent a full and fair test of the intervention.
The first pre-test of the intervention will be conducted among young people (age ≤ 25 years) visiting the public sexual health care centre South Limburg for Ct treatment.
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