Face-to-face validation of the final version was made to ensure that it was conceivable and had satisfactory internal consistency. Participation rate and rate of missing values were tested in a pilot study. The main study, the quantitative phase, was carried out during January–October 2006. Eligible women who gave informed consent received a postal questionnaire. Confidentiality was maintained by numbering the questionnaires.
Survivorship Questionnaire Development
Face-to-face validation of the final version was made to ensure that it was conceivable and had satisfactory internal consistency. Participation rate and rate of missing values were tested in a pilot study. The main study, the quantitative phase, was carried out during January–October 2006. Eligible women who gave informed consent received a postal questionnaire. Confidentiality was maintained by numbering the questionnaires.
Corresponding Organization : Karolinska Institutet
Other organizations : University of Gothenburg, Karolinska University Hospital
Protocol cited in 5 other protocols
Variable analysis
- None explicitly mentioned
- Incidence, prevalence, intensity and duration of symptoms from the gastrointestinal tract, urinary bladder, genitals, pelvic bones, abdomen and legs
- Impact of symptoms on different aspects of social functioning
- None explicitly mentioned
- Face-to-face validation of the final version of the questionnaire was done to ensure it was conceivable and had satisfactory internal consistency.
- Participation rate and rate of missing values were tested in a pilot study.
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