The Impact of Breast Surgery on Patients' Quality of Life

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Basel, Switzerland

About this trial

The investigators aim to document the surgery-specific and overall Quality of life parameters of patients undergoing all types of breast surgery at the University Hospital of Basel

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

adults who underwent any type of breast surgery at the University Hospital of Basel

Disqualifiers

Patients under the age of 18 years, without general consent or written informed consent, with insufficient language comprehension or other factors limiting their ability to co-operate in the study

Trial population

patients who underwent breast surgery at the University Hospital Basel from 2014 onwards

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Patient satisfaction

five point likert-scale for satisfaction ( psychometric survey response scale ranging from "Strongly Disagree" to "Strongly Agree". The format includes: 1. Strongly Disagree, 2. Disagree, 3. Neutral (or Neither Agree nor Disagree), 4. Agree, and 5. Strongly Agree Descriptive measures using patient-reported outcome measures (BREAST-Q, McGill short form, EQ-5D-5L)

Time frame
up to 10 years
2

Patient reported quality of life

Descriptive measures using patient-reported outcome measures (BREAST-Q, McGill short form, EQ-5D-5L)

Time frame
up to 10 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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