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. 2014 Jul 26;41(1):30–43. doi: 10.1093/schbul/sbu108

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© The Author 2014. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Fig. 3. — Symptom and functional levels across study intervals. CLR, clinically lower risk, baseline n = 87. CHR, clinically higher risk, baseline n = 205. EFEP, early first-episode psychosis, baseline n = 45. Data points represent mean raw (unadjusted) scores for each subgroup at the respective assessment date.

Fig. 3. — Symptom and functional levels across study intervals. CLR, clinically lower risk, baseline n = 87. CHR, clinically higher risk, baseline n = 205. EFEP, early first-episode psychosis, baseline n = 45. Data points represent mean raw (unadjusted) scores for each subgroup at the respective assessment date.