Clinical trial · Observational
The Impact of SPC on Advanced Breast Cancer Patients
The Influence of Specialist Palliative Care on the Exacerbation of Negative Symptoms, Life Quality and Performance Status of Patients With Advanced Breast Cancer
NCT03612934CI-TRIAL-00034107completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The aim of this prospective, observational study is the evaluation of the effectiveness of a 14-day Specialist Palliative Care therapy in participants with advanced breast cancer carried out in a stationary palliative care unit in Poland. The length of the entire study will be 36 months.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Cancer, Breast | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Palliative Care | — | UNRESOLVED | — |
| Quality of Life | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Specialist Palliative Care | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- patients under the age of 65 years
- description
- patients under the age of 65 years
- interventionNames
- Procedure: Specialist Palliative Care
- label
- patients at the age of 65 years and over
- description
- patients at the age of 65 years and over
- interventionNames
- Procedure: Specialist Palliative Care
Primary outcomes (3)
- measure
- Variation of intensification of patients negative symptoms before and after SPC
- timeFrame
- 14 days
- description
- intensification of patients negative symptoms was assessed by Edmonton Symptom Assessment System (esas)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 33 Years
- Maximum age
- 91 Years
Show eligibility criteria text
Inclusion Criteria: the patient's conscious consent for examination and the ability to fill in the form by the patient herself. \- Exclusion Criteria: * patients with cognitive disturbances disabling credible answers in the questionnaire, deceased patients or those discharged from the ward before 14 days of hospitalisation.
References
Publications (0)
Data not yet available
No reference posted for this study.