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Two groups of responders on the noise annoyance questionnaire attended the laboratory for the second stage involving a determination of the uncomfortable loudness level (ULL) by two methods (Békésy and analogue adjustment) and for two types of sound source (white noise and a 1 kHz tone).
Of this group, 498 men and 468 women from East Hertfordshire completed a questionnaire, attended a clinic visit, and underwent bone density measurement.
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Each was asked to complete a questionnaire, attend a research facility for physical assessment and an overnight sleep study, wear activity monitors for a week, and to maintain a sleep and activity diary over this week.
Eligible subjects for this study were women who had completed study questionnaires, attended study clinics, were not currently taking oral contraceptives, and not pregnant or breast feeding at the time of clinic attendance.
The pre-publication history for this paper can be accessed here: http://www.biomedcentral.com/1471-2458/10/532/prepub We are grateful to experts and representatives of government ministries who completed questionnaires, attended workshops and offered their insight and expert opinions.
One month after the workshop, the same survey delivery procedure was performed to deliver follow-up questionnaires to all physicians who filled out the baseline questionnaire and attended the workshop.
Of the 74 patients, 52 returned the patient questionnaire and attended the clinical examination.
All participants were mailed a questionnaire and attended a clinical examination (for details see ref. 22).
In all, 171 students completed the questionnaire and attended the lab for testing.
There are some cases where an individual self-administered questionnaire occurred (attended by an interviewer).
Baseline data are presented for women who returned a baseline questionnaire and attended a clinic appointment (Table 1).
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