The European Palliative Care Cancer Symptom Study (EPCCS)
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Purpose
The rising incidence of cancer and the rapidly increasing number of people living longer with incurable disease, accentuates the need for optimal symptom management throughout the disease trajectory. Thanks to the medical and technological development, and the increased interest in palliative care research, palliative medicine has gradually become more evidence based. Patients with advanced cancer experience multiple symptoms at the time with fluctuating intensity and severity. Pain, fatigue, nausea/vomiting, dyspnea, loss of appetite and depression are among the most common and experienced by more than 50%. However, the prevalence rates of these symptoms vary considerably across studies, with a range from 35 to 90 % for pain as an example. These differences may in part be explained by different assessment tools, study methods and design and population characteristics. There is also lack of agreed-upon, common criteria to describe the main characteristics of a palliative care cancer population and few standardized tools for assessment and classification of symptoms exist. These shortcomings limit the possibility to design randomized controlled treatment trials in palliative care; the optimal way to improve clinical symptom management. To do this, a better understanding of how symptoms evolve and how they should be assessed and classified throughout the palliative care disease trajectory is important, supplemented with registrations of the treatment provided. The primary aim of this international research project the European Palliative Care Cancer Symptom study (EPCCS) is to extend the knowledge about and gain new insight in the prevalence and development of the most frequent cancer related symptoms during the course of disease, in a large sample of palliative care cancer patients. The clinical usefulness of the new assessment and classification system developed by the European Palliative Care Research Collaborative (EPCRC) / European Association for Palliative Care Research Network (EAPC RN) will be examined and data on the organization and delivery of palliative care at participating centers will be collected. The project also aims to further develop and consolidate international research collaboration through the European Palliative Care Research Centre (PRC). Taken together, these efforts will increase the understanding of the palliative disease trajectory and provide necessary knowledge and structure for future randomized controlled trials (RCTs)
| Condition |
|---|
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Cancer |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | The European Palliative Care Cancer Symptom Study (EPCCS). A Prospective Data Collection |
- change in cancer symptoms [ Time Frame: up to 6 months ] [ Designated as safety issue: No ]assessment and classification system developed by the European Palliative Care Research Collaborative (EPCRC) / European Association for Palliative Care Research Network (EAPC RN)
| Estimated Enrollment: | 1200 |
| Study Start Date: | June 2011 |
| Estimated Study Completion Date: | June 2015 |
| Estimated Primary Completion Date: | December 2014 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
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Palliative care cancer patients
Inclusion criteria are: Patient has a cancer diagnosis (radiological, histological, cytological or operative evidence), local, loco-regional or metastatic disease, defined as a palliative care patient; enrolled in a palliative care programme, age 18 years or older, able to provide written informed consent, able to complete the data collection tool, preferably without help, available for follow up registration |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
The popuation consists of patients with incurable cancers who are enrolled in a palliative care programme. They will be identified upon referral for non-curative cancer treatment/palliative care to the centre, department, out-patient clinic, daycare centre, hospice, or home-based care, depending on the palliaitve care organization model at the participating centres. Patients will be followed every 4 weeks (3-5) for at least 6 months, or until death
Inclusion Criteria:
- Patient has a cancer diagnosis (radiological, histological, cytological or operative evidence)
- Local, loco-regional or metastatic disease
- Defined as a palliative care patient; enrolled in a palliative care programme
- Age 18 years or older
- Able to provide written informed consent
- Able to complete the data collection tool, preferably without help
- Available for follow up registration
Exclusion Criteria:
- Patients receiving anti-cancer treatment with a curative intent
- Patients who are unable to complete the registration due to language problems or severe physical problems
- Patients who have psychotic disorders or obvious cognitive impairment
- Patients who cannot come for regular follow-up visits, due to geographical or social reasons
Contacts and Locations| Contact: Marianne Jensen Hjermstad | +47 23026828 | m.j.hjermstad@medisin.uio.no |
| Contact: Stein Kaasa | +47 72826486 | stein.kaasa@ntnu.no |
| Norway | |
| Norwegian University of Science and Technology | Recruiting |
| Trondheim, Norway, 7491 | |
| Contact: Marianne Jensen Hjermstad +47 23026828 m.j.hjermstad@medisin.uio.no | |
| Contact: Stein Kaasa +47 72826486 stein.kaasa@ntnu.no | |
| Principal Investigator: | Stein Kaasa, Professor MD | Norwegian University of Science and Technology |
| Principal Investigator: | Marianne J Hjermstad, Senior researcher/PhD | Norwegian University of Science and Technology |
More Information
No publications provided
| Responsible Party: | Norwegian University of Science and Technology |
| ClinicalTrials.gov Identifier: | NCT01362816 History of Changes |
| Other Study ID Numbers: | 2010/2945-3 |
| Study First Received: | May 27, 2011 |
| Last Updated: | January 9, 2013 |
| Health Authority: | Norway: Ministry of Health and Care Services |
ClinicalTrials.gov processed this record on May 19, 2013