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The studies included showed substantial heterogeneity regarding objectives and study design, location and setting, numbers and characteristics of participants, screening personnel, methods of recruitment and types of data collected.
Participants screening positive for ADHD were invited to complete a research diagnostic interview assessment.
Participants screening viewed a 14 minute multimedia decision aid that addresses CRC screening rationale, recommendations, and options.
At the end of the trial we intend to assess participants' screening attendance from screening records as well.
In addition, a number of categorical questions were asked to identify participant's previous exposure to the NCSP and to determine the intention of participants screening behaviour.
Participants screening positive for new-onset depression and anxiety/panic were identified using the PRIME-MD Patient Health Questionnaire (PHQ) [ 26– 29].
Similar(42)
Of the 1,781 participants screened, 848 were ineligible (47.6%), 426 (23.9%) were eligible but did not enroll in the study, and 507 (28.5%) were eventually randomized.
Of 55 participants screened out through laboratory testing for Protocol 010, 28 (50.9%) had hyperbilirubinemia (Table 3).
Participants screened for exercise.
All 20 participants screened entered and completed the study.
Of 512 participants screened, 456 were randomized (2 : 1) to IDeg (303) or IDet (153).
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