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The European Palliative Care Research Collaborative - Computerised Symptom Assessment and Classification of Pain, Depression and Physical Function (Cachexia) (EPCRC - CSA)


N/A
18 Years
N/A
Not Enrolling
Both
Cachexia, Depression, Pain, Unspecified Adult Solid Tumor, Protocol Specific

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Trial Information

The European Palliative Care Research Collaborative - Computerised Symptom Assessment and Classification of Pain, Depression and Physical Function (Cachexia) (EPCRC - CSA)


OBJECTIVES:

- Determine the feasibility of applying a computer-based system for symptom assessment
and classification in palliative cancer care in patients with metastatic and/or
advanced cancer.

- Examine hypothesized differences across groups related to acceptance of computers
(i.e., age, culture, stage of disease, cognitive and physical function, etc.).

- Examine the general user-friendliness of the tool.

- Test and validate the performance of selected domains and items for classification and
assessment of pain and cachexia.

- Explore the validity of domains and items for depression.

OUTLINE: This is a multicenter study.

All patients undergo computer-based assessments of general symptoms by the Edmonton Symptom
Assessment System (ESAS) and the European Organization for Research and Treatment of Cancer
Core Quality of Life (EORTC QLQ C30) questionnaires and assessment of physical function,
appetite/weight loss, and depression by the Brief Patient Health Questionnaire 9 (PRIME-MD
PHQ9). Patients who score ≥ 1 (on a 0-10 numerical rating score) on the pain screening
question with or without occurrence of breakthrough pain (BTP), undergo the Alberta BTP
Assessment tool assessing precipitating factors for pain, time to pain relief after intake
of medication, and satisfaction with medication. Patients complete questions regarding
user-friendliness and feasibility of using the computer at the end of their session.

Inclusion Criteria


DISEASE CHARACTERISTICS:

- Diagnosis of incurable cancer, including patients receiving life-prolonging treatment

- Metastatic and/or advanced locoregional disease

PATIENT CHARACTERISTICS:

- Able to provide written informed consent

- Fluent in the language used at the study site

PRIOR CONCURRENT THERAPY:

- No prior inclusion in this study

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Cross-Sectional

Outcome Measure:

Feasibility of applying a computer based system for symptom assessment and classification in palliative cancer care

Outcome Time Frame:

Sept 2008-December 2009

Safety Issue:

No

Principal Investigator

Stein Kaasa, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Norwegian University of Science and Technology

Authority:

Norway: Regional Ethics Commitee

Study ID:

CDR0000648077

NCT ID:

NCT00972634

Start Date:

October 2008

Completion Date:

December 2009

Related Keywords:

  • Cachexia
  • Depression
  • Pain
  • Unspecified Adult Solid Tumor, Protocol Specific
  • depression
  • cachexia
  • pain
  • unspecified adult solid tumor, protocol specific
  • Cachexia
  • Depression
  • Depressive Disorder

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