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Fig. 1 A summary of the questionnaire outcomes (see text).
Table 4 summarises the questionnaire outcomes.
Other experience questionnaire outcomes are reported in Table 4.
The ESS and Berlin questionnaire outcomes were not associated with either AHI cut-point.
Point-of-care fingerstick capillary blood testing was performed to validate the risk questionnaire outcomes.
Four studies reported self-report questionnaire outcomes for depression [ 11, 12, 14, 15].
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The Zurich Claudication Questionnaire outcome of the patients reoperated after interspinous process device placement did not differ significantly from that of the other patients (P=0.08).
The sample size calculation was based on the parent-reported questionnaire outcome of the original study, the Child Behavior Check List (CBCL).
Participants will also be contacted by email or phone to obtain questionnaire outcome measurements only at 12, 18, 24 and 30 weeks.
All participants completed the questionnaire outcome measures (BDI-II, PHQ-9, K-10, CEQ, ERS and SDS) at 1-week post treatment and at 3-months follow up.
If participants became unable to attend the posttreatment assessment, questionnaire outcome measures were completed online (n = 8) or by mail (n = 7).
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CEO of Professional Science Editing for Scientists @ prosciediting.com