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For parents and adolescents, measures were collected on pretreatment and posttreatment, with an additional follow-up assessment for parents at 3 months after treatment.
All self-reported measures were collected on the same day as the muscle tests were performed.
In some cases these measures were collected on the next week if a subject failed to attend a scheduled visit.
Outcome measures were collected on the same day on both occasions and baseline outcomes were assessed before implementation of the intervention.
The psychosocial measures were collected on visit 1 (baseline), visit 4 (12 weeks) and visit 6 (24 weeks) for both groups.
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Within-subject design 2 (direction: positive, negative) × 4 (distance: 20%, 40%, 60 %, 80) was employed and individual measures were collected for 230 participants on each experimental level.
Repeated measures were collected to assess variability in PCE exposure on consecutive days (Wednesday, Thursday, and Friday) after at least two days of exposure.
The measured data was collected on 19 July 2016 by a frame-camera mounted on an unmanned aerial vehicle (UAV) over a potato field, where eight experimental plots of 30 × 30 m were designed with different fertilization levels.
Course of illness measures were collected and focused on the phenotype domains of psychosis, suicidality, mood instability, comorbid anxiety, and comorbid substance abuse.
Participants were requested to complete a number of questionnaires, they were filmed during the experiment with the aim to record eye movements, and additionally a number of driving performance measures were collected and saved on the simulator computer.
Subjects were seen for safety visits at weeks 1, 2, and 3. Outcome measures were collected after 4 weeks on AZD0530 or placebo, including measures of safety and tolerability, CSF drug concentration, clinical efficacy measures, and F-FDG PET imaging.
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