Observational study of the informed consent for outpatient chemotherapy - A multi-methods research using a questionnaire and an observational approach

Observational study of the informed consent for outpatient chemotherapy - A multi-methods research using a questionnaire and an observational approach - Multi-methods Observational Research Employing both qualitative and quantitative approach for outpatient chemotherapy IC (MORE-IC)

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000001625

Enrollment

Registered

2009-01-10

Start date

2009-01-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer, Breast Cancer

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients are enrolled in the study if they meet all of the following criteria 1) Written informed consent 2) They are 20 years old or older 3) Patients who are eligible for the study by their physicians

Exclusion criteria

Exclusion criteria: Patients who are disqualified the study by their physicians

Design outcomes

Primary

Measure	Time frame
The types of thematic units generated by content analysis of IC and the frequency of the categories	—

Secondary

Measure	Time frame
Co-relation between the following data; 1) the categories of patient's psychological state from questionnaire assessment before IC 2) the frequency of the categories generated by content analysis 3) the subjective evaluation scores after IC	—

Countries

Japan

Contacts

Public ContactHatta Taichi

Kyoto University Graduate School of Medicine Clinical Inovative Medicine

hatta1@kuhp.kyoto-u.ac.jp075-751-4739

Outcome results