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Clinical Trials/RBR-87bg28
RBR-87bg28
Not Yet Recruiting
N/A

Effectiveness of a psychoeducation program to reduce barriers and stigmas of patients with breast cancer in relation to palliative care

Fundação Pio XII0 sitesAugust 18, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
eoplasms, Breast Neoplasms
Sponsor
Fundação Pio XII
Status
Not Yet Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 18, 2020
End Date
December 20, 2023
Last Updated
2 years ago
Study Type
Intervention
Sex
Female

Investigators

Sponsor
Fundação Pio XII

Eligibility Criteria

Inclusion Criteria

  • Women; aged between 18 and 75 years; Present a diagnosis of advanced breast cancer and have knowledge of the disease; being under palliative chemotherapy with Paclitaxel and who do not meet the criteria for immediate palliative care, in accordance with the Palliative Care Referral Protocol in force at the institution; With life expectancy greater than 6 months, at the discretion of the clinical oncologist; Be classified according to the functionality scale of the Estern Cooperative Oncology Group, with an index greater than 2 on the scale.

Exclusion Criteria

  • Being under drug treatment for mental disorders; Manifest cognitive, attention, language and orientation deficits, preventing questionnaires and instruments, according to screening criteria of the Mini Mental State Examination, considering cut\-off points of 17 points for illiterates, 22 points for 1 to 4 years of age. schooling, 24 points from 5 to 8 years of schooling and 26 points for 9 or more years of schooling; Need assistance or have an appointment at the palliative care unit due to advanced cancer, in accordance with the Palliative Care Referral Protocol; Have a diagnosis of advanced cancer, with no possibility of cure and associated with any of the criteria for referral for palliative care according to PECP; Present any comorbidity that, in the opinion of the researchers, prohibits the patient from participating in the study; Weekly visits to the hospital are not available.

Outcomes

Primary Outcomes

Not specified

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