Effect of Early Palliative Care on Quality of Life of Patients With Advanced Cancer: a Randomised Controlled Trial. (IPaC)

University Ghent

Status

Completed

Conditions

Life-limiting Cancer With Prognosis of Approximately 1 Year

Treatments

Behavioral: Standard oncologic care

Behavioral: Interventional palliative care

Study type

Interventional

Funder types

Other

Identifiers

NCT01865396

2012/865

Details and patient eligibility

About

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.

Enrollment

268 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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):
- Metastatic and advanced pancreatic, stomach, oesophageal and biliary tract adenocarcinoma;
- Metastatic or advanced NSCLC (stage IIIB or IV) or metastatic SCLC,
- Malignant pleural mesothelioma
- Metastatic or advanced head and neck cancer (stage III or IV)
Patients are within 12 weeks of progression after receiving treatment and have an prognosis of approximately 1 year:
- Metastatic and locally advanced colorectal cancer, with progression after second line treatment
- Metastatic or advanced prostate carcinoma, after second line treatment
- Advanced breast cancer with visceral and/or brain metastasis, with progression on second or third line treatment
- Metastatic melanoma,
- Metastatic or advanced kidney cancer,
- Metastatic or advanced bladder cancer after first line treatment,

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

Patients under 18 years old
Patients with impaired cognition
Patients who met the palliative support team more then once or had a consultation within 6 months of inclusion.