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ongitudinal study for observing the process of informed consent for outpatient chemotherapy

Not Applicable
Conditions
ung Cancer, Breast Cancer
Registration Number
JPRN-UMIN000007607
Lead Sponsor
Kyoto University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Not provided

Exclusion Criteria

Patients who are disqualified the study by their physicians.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Questionnaire of Achievement Motive for Medical Treatment. Subjective score for process of informed consent.
Secondary Outcome Measures
NameTimeMethod
1) scales regarding self-image. 2) observation record during the IC process, including audio-taped and transcribed data.
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