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The reference categories used were the 30 34 year age group, the data collection from 2009 10 and the dentist birth cohort that was aged 25 29 years in 1983.
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Figure 1 illustrates the treatment received by the intervention group, the waitlist control condition received by the control group, and the data collection points of the study.
Although the research staff was not informed of the group assignment, the data collection schedule (data at 4 weeks were collected only from participants who were receiving treatment) did not allow for blinding to be maintained.
The immediate treatment received by the intervention group, the wait-list control condition received by the control group, and the data collection points is shown in Figure 1.
Respondent burden was a key consideration for this participant group and the data collection procedures were designed to minimise this.
Detailed descriptions of the selection procedure for the intervention and the control group and the data collection procedure are given in Figure 1.
Outcome data was collected by a RA who was initially blinded to group allocation, however, commonly participants would reveal their group allocation during the data collection process.
JY and staff of the research group assisted with the data collection.
The study applied in-depth interviews and focus group discussions in the data collection.
PJV and BvM were responsible for the focus group interview and the data collection (three Delphi survey rounds).
WS and AR developed the proposal and data collection methodology based on international Collaborative group, and oversaw the data collection and analysis.
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