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. 2017 Oct 12;6(10):e197. doi: 10.2196/resprot.8051

Table 2.

Data collection schedule for outcomes measures.

Measure Data collection method n Baseline 2 months 6 months 12 months
Use data Log data analytics software 610 Throughout study duration
Demographic data Web-based questionnaire 400 x


Clinical data Chart review 400 x


Credibility/Expectancy questionnaire Web-based questionnaire 400 x


Expanded Prostate Cancer Composite Web-based questionnaire 400 x x x x
Prostate Cancer-Related Quality of Life Scales Web-based questionnaire 400 x


Service Satisfaction Scale for Cancer Care Web-based questionnaire 400 x x x x
Supportive Care Needs Survey Web-based questionnaire 400 x x x x
Self-Efficacy for Managing Chronic
Disease Scale
Web-based questionnaire 400 x x x x
Memorial Anxiety Scale for Prostate Cancer Web-based questionnaire 400 x x x x
Modified UTAUTa survey Web-based questionnaire 400


x
Patient qualitative interviews (1) Semistructured live interview (2) Qualitative observation of app use 20


x
Caregiver qualitative interviews Semistructured live interview 10


x
Clinician System and Use Assessment Survey Web-based questionnaire 10


x

aUTAUT: unified theory of acceptance and use of technology.