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. 2013 Jan 7;15(1):e5. doi: 10.2196/jmir.2249

Table 7.

Between-group effect sizes (ES) after the smartphone intervention (T3) and at 5-month follow-up (T4).

Outcome measurea ES at T3 P valueb ES at T4 P valueb
Primary




PCS (ITT and LOCF) 0.40 .01 0.36 .05

PCS (per protocol) 0.87 < .001 0.74 .003
Secondary (per protocol)




CPAQ 0.62 .007 0.54 .02

FIQ 0.21 .35 0.75 .001

SF-8, physical –0.15 .64 0.35 .13

SF-8, mental 0.63 .005 0.43 .06

GHQ-12 0.03 .56 0.33 .16

CPVI 0.63 .005 0.40 .08

Pain, VAS –0.15 .49 0.28 .22

Fatigue, VAS 0.04 .87 0.41 .07

Sleep disturbance, VAS 0.19 .36 0.55 .02

a PCS: pain catastrophizing scale; ITT: intention-to-treat; LOCF: last observation carried forward; CPAQ: Chronic Pain Acceptance Questionnaire; FIQ: Fibromyalgia Impact Questionnaire; SF-8: Short-Form Health Survey; GHQ-12: General Health Questionnaire; CPVI: Chronic Pain Values Inventory; and VAS: visual analog scale.

b P values for independent t tests or nonparametric tests.