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As mentioned earlier a former research assistant from the controlled study was employed as training instructor at the private sector company (author PM of this paper).
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Methods: A case-controlled cross-sectional study design was employed: 54 patients with GAD and 64 healthy controls were recruited.
In order to evaluate the overall effectiveness of the intervention, a randomised controlled design was employed.
Design: A single-blind placebo-controlled design was employed in this study.
An observational, retrospective, non-controlled study was conducted.
A case-controlled study was undertaken.
Design: A pragmatic randomised controlled trial (RCT) design was employed with two study arms: LiFE program (intervention) and the current exercise program (control).
The smart controlled release of magnetic nanocarriers was employed via HFMF.
In that study a similar power output was employed (150 W), with the temperature maintained using a thermostatically-controlled glass reaction vessel.
Controlled conditions were employed throughout the study: insulin aspart was used by all participants, subcutaneous infusion sites were changed on the evening before each 2-day study block, catheter site (e.g., hip or stomach) remained constant in a given individual over the entire study period, and activity was limited to sedentary activities in a research unit.
The modified BI[ 8] was employed in this study as this was the version already in use in a concurrent randomised controlled trial that included the same patient population at The Northern Hospital.
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