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Informed consent was conducted at the NMRCD laboratory before the start of each focus group discussion.
Participants were asked to give their informed consent at the start of each focus group session.
Informed consent was obtained from all participants prior to the start of each focus group.
At the start of each focus group, the facilitator explained the purpose of the session and asked physicians to sign a statement of informed consent.
At the start of each focus group the PW intervention for sick-listed employees with low back pain was presented and the theoretical framework was introduced (SHO).
At the start of each focus group discussion, caregivers completed a 48-item GERD Caregiver Informational Survey, developed for this study, which contained questions about the caregiver's and child's demographic, socioeconomic and clinical profile.
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At the start-up of each focus group, the aim and conditions were clarified and informed consent was achieved.
We administered brief written questionnaires at the start and end of each focus group, including demographics, preferred involvement in decision making about screening (control preferences scale), 49 and items to assess basic background knowledge and understanding of content presented (see appendix 3 on bmj.com for key items from questionnaires 1 and 2).
The researcher was knowledgeable about healthcare improvement but uninvolved in the development or dissemination of the SQUIRE Guidelines prior to beginning the research, and she introduced herself as such at the start of each interview and focus group.
Written consent was obtained from each participant at the start of the focus group or interview.
They were given a second copy and the opportunity to ask questions about the study, and asked to sign the form at the start of the focus group.
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