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| Name | Class |
|---|---|
| Vrije Universiteit Brussel | OTHER |
| Fund for Scientific Research, Flanders, Belgium | OTHER |
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The World Health Organization (WHO) defines palliative care as an approach to improve the quality of life of patients and their families facing life-threatening illness, through prevention and relief of pain and of physical, psychosocial and spiritual problems. The WHO stresses that palliative care is applicable early in the course of the illness together with other therapies that are intended to cure or prolong life, such as chemotherapy or radiation therapy. For the benefit of the patient, palliative care is however often given (too) late in the course of the disease of incurably ill patients.
The aim of our study is to measure the effect of interventional palliative care on quality of life, mood and end-of-life care of patients with advanced cancer and their families. These patients have a limited life expectancy and a high symptom burden, this leads us to suggest that these patients may be benefited with palliative care soon after diagnosis of metastatic disease (interventional palliative care).
The research design of this study is a randomized controlled trial with, on the one hand, an intervention group in which patients and their families receive interventional palliative care in combination with standard cancer care and on the other hand a control group in which patients and their families receive only standard oncologic care. Participants in the intervention group will meet the palliative support team shortly after diagnosis. Afterwards, the palliative support will meet them at least once a month. This intervention focuses on topics such illness understanding, symptom management, decision making and coping with the disease. Participants in the control group will only meet with the palliative support team at the patient's own request or after referral by the oncologist or the nursing staff.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| early palliative care | Experimental | Interventional palliative care, after diagnosis and once a month. |
|
| Standard care | Active Comparator | Patients will receive the standard oncologic care. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Interventional palliative care | Behavioral | Palliative support team will meet the patient soon after diagnosis of incurable disease and will meet the patient at least once a month. The patient will also receive the standard oncologic care. |
| Measure | Description | Time Frame |
|---|---|---|
| Quality of life of the patient and his family caregiver at baseline. | This will be measured with validated questionnaires(EORTC-QLQ C30, McGill QoL, SF-36). | at baseline |
| Quality of life of the patient and his family caregiver at 12 weeks. | This will be measured with validated questionnaires (EORTC-QLQ C30, McGill QoL, SF-36). | at 12 weeks |
| Quality of life of the patient and his family caregiver, 6-weekly after 12 weeks. | This will be measured with validated questionnaires (EORTC-QLQ C30, McGill QoL, SF-36). | 6-weekly after 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Influence of palliative care on mood and illness-understanding of patients and family caregivers at baseline. | This will be measured with validated questionnaires (HADS, PHQ-9, illness understanding). | at baseline. |
| Influence of palliative care on mood and illness-understanding of patients and family caregivers at 12 weeks. |
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Inclusion Criteria:
Patients with life-limiting cancer (prognosis of approximately 1 year) are eligible if:
Patients are within 12 weeks of referral from an other hospital after receiving first line treatment or within 8 to 12 weeks of a new diagnosis (histological and cytological confirmed):
Patients are within 12 weeks of progression after receiving treatment and have an prognosis of approximately 1 year:
An Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2 and ability to read and respond to questions in Dutch.
Exclusion criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Simon Vanbelle, MD, PhD | University Hospital, Ghent | Study Director |
| Luc Deliens, PhD, MD | Vrije Universiteit Brussel and Ghent University | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Ghent University Hospital | Ghent | 9000 | Belgium |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 29402701 | Derived | Vanbutsele G, Pardon K, Van Belle S, Surmont V, De Laat M, Colman R, Eecloo K, Cocquyt V, Geboes K, Deliens L. Effect of early and systematic integration of palliative care in patients with advanced cancer: a randomised controlled trial. Lancet Oncol. 2018 Mar;19(3):394-404. doi: 10.1016/S1470-2045(18)30060-3. Epub 2018 Feb 3. | |
| 26666301 |
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| Standard oncologic care | Behavioral | Patients will receive standard oncologic care. |
|
This will be measured with validated questionnaires (HADS, PHQ-9, illness understanding). |
| at 12 weeks |
| Influence of palliative care on mood and illness-understanding of patients and family caregivers 6-weekly, after 12 weeks. | This will be measured with validated questionnaires (HADS, PHQ-9, illness understanding). | 6-weekly, after 12 weeks. |
| Influence of palliative care on the decision of physicians with regards to end-of-life-care. | This will be measured with the questionnaire for decisions wuth regards to end-of-life decision making for physicians. | after death of patient |
| Vanbutsele G, Van Belle S, De Laat M, Surmont V, Geboes K, Eecloo K, Pardon K, Deliens L. The systematic early integration of palliative care into multidisciplinary oncology care in the hospital setting (IPAC), a randomized controlled trial: the study protocol. BMC Health Serv Res. 2015 Dec 15;15:554. doi: 10.1186/s12913-015-1207-3. |