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Clinical Trials/NCT02746666
NCT02746666
Completed
N/A

Influence of a Clinical Pharmacist's Intervention on Quality of Life of a Breast Cancer Patient Under Adjuvant Chemotherapy

University Hospital "Sestre Milosrdnice"0 sites70 target enrollmentApril 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Breast Cancer, Quality of Life
Sponsor
University Hospital "Sestre Milosrdnice"
Enrollment
70
Primary Endpoint
changes in quality of life of a breast cancer patient under chemotherapy, after a clinical pharmacist's behavioral intervention, measured by EORTC B23 questionnaire
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to investigate the impact of pharmacist behavioral intervention's influence on breast cancer patients' quality of life. Croatian randomized controlled trial. Targeted population: general population of breast cancer patients under the first adjuvant anthracycline chemotherapy. Primary outcome: difference in EORTC QLQ-BR23 questionnaire result from the baseline to after 3 week cycle.

Registry
clinicaltrials.gov
Start Date
April 2016
End Date
June 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
University Hospital "Sestre Milosrdnice"
Responsible Party
Principal Investigator
Principal Investigator

Robert Šeparović

MD PHD

University Hospital "Sestre Milosrdnice"

Eligibility Criteria

Inclusion Criteria

  • Early breast cancer
  • First adjuvant chemotherapy
  • Chemotherapy protocol: anthracycline x 4

Exclusion Criteria

  • Cardiovascular comorbidities
  • Regular nausea or vomiting during six months before enrollment
  • Unable to answer the quality of life questionnaire on their own

Outcomes

Primary Outcomes

changes in quality of life of a breast cancer patient under chemotherapy, after a clinical pharmacist's behavioral intervention, measured by EORTC B23 questionnaire

Time Frame: up to two months

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