Skip to main content
. 2018 Sep 26;44(2):111–119. doi: 10.1503/jpn.170201

Table 1.

Demographic and clinical characteristics of study participants

Measure Healthy volunteers (n = 18) People at clinical high risk for psychosis (n = 35) Statistical test p value
Age, yr, mean ± SD 21.28 ± 1.99 20.57 ± 1.63 F = 1.91 p = 0.17
Sex, male: female 6:12 19:16 χ2 = 2.09 p = 0.15
Current drug use, n*
 Nicotine 0 8
 Cannabis 0 4
Lifetime history of recreational drug use (use > 10 times), n
 Cannabis 0 17
 MDMA 0 1
 Cocaine 0 1
 LSD 0 1
 Barbiturate 0 1
Antipsychotic use, n 0 5
SOPS, mean ± SD
 Total 36.03 ± 11.81
 Positive 11.20 ± 3.76
 Negative 11.37 ± 5.94
 Disorganization 3.74 ± 2.65
 General 8.86 ± 4.31
AES, mean ± SD 39.06 ± 9.19
CDSS, mean ± SD 5.51 ± 4.03
RBANS, total, mean ± SD 90.94 ± 13.95

AES = Apathy Evaluation Scale; CDSS = Calgary Depression Scale for Schizophrenia; CHR = clinical high risk for psychosis; LSD = lysergic acid diethylamide; MDMA = 3,4-methylenedioxymethamphetamine (ecstasy); SOPS = Scale of Psychosis-Risk Symptoms; RBANS = Repeatable Battery for the Assessment of Neuropsychological Status; SD = standard deviation.

*

All participants underwent a urine drug screen at baseline for cannabis, ethanol, methadone and cocaine. Baseline results were negative, except for 1 member of the CHR group with a positive result for benzodiazepine, and 4 members of the CHR group with a positive result for cannabis.

Participants at clinical high risk for psychosis who were currently on antipsychotic treatment: 0.5 mg risperidone (n = 1), 1.0 mg risperidone (n = 2), 75 mg quetiapine (n = 1), and 5 mg aripiprazole (n = 1).

Score missing for 2 participants.