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Eighteen studies were descriptive studies (no design study, just a plain description of the interventions, context factors, implementation process or effectiveness).
This paper provides a description of the interventions that were implemented.
Concerning other key methodological aspects, weighted overall proportions of RCTs with adequately reported items were as follows: eligibility criteria (81%), secondary outcomes (46%), harm (5%) follow-up duration (62%), description of the interventions (53%) and sample size calculation (1%).
Arguably the two most important pieces of information about a clinical trial that need to be registered are the description of the interventions being compared, and the outcomes upon which any conclusion about the safety and effectiveness of the interventions will be made.
A detailed description of the interventions is provided below.
Detailed description of the interventions and their systematic development is provided in our partner paper [ 13].
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The detailed rationale and description of the intervention are described elsewhere (Sylvia et al. 2011).
Description of the intervention protocol and the schedule of intervention meetings: Table 5 Description of the intervention protocol Meeting Objective Procedures Attraction Introduce the project proposal and sensitize workers, arousing interest in joining the intervention.
Description of the intervention was not always sufficient to allow replication.
Inadequate descriptions of interventions Provide a detailed description of the intervention (including any components) in such as way that the intervention could be replicated (e.g., duration and frequency of sessions, curriculum, stipends, and trainee accreditation).
A more detailed description of the intervention and study can be found elsewhere (Kinner et al. 2013; Kinner et al. 2014).
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