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Telemedically augmented palliative care: Empowerment for patients with non-small cell lung cancer and their family caregivers

Not Applicable
Recruiting
Conditions
C34
Malignant neoplasm of bronchus and lung
Registration Number
DRKS00004899
Lead Sponsor
Medizinische Universität Wien
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

PATIENTS:

•Patients of each sex between 18 and 75 years

•Patients with histologically or cytologically confirmed incurable NSCLC, stage IV

•Inclusion has to be before the first chemotherapy is received

•Patients with an ECOG performance status of 0, 1 or 2 (with 0 indicating that the patient is asymptomatic, 1 that the patient is symptomatic but fully ambulatory, and 2 that the patient is symptomatic and in bed <50 % of the day)

•Patients without cognitive impairment

FAMILY CAREGIVERS:

(for every patient, one of his/her caregivers will be included)

•Family caregivers without cognitive impairment

Exclusion Criteria

PATIENTS:

•All patients without signed informed consent (including persons unable to give consent)

•Patients with prior chemotherapy for metastatic disease

•Patients with ECOG > 2

•Patients with cognitive impairment

FAMILY CAREGIVERS:

•Family caregivers without signed informed consent (including persons unable to give consent)

•Family caregivers with cognitive impairment

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improve patients’ and family caregivers’ quality of life via validated questionnaires (HADS, FAMCARE, EORTC<br>QLQ-­-C15-­-PAL) at three different points of time: baseline (recruitment), 10 weeks after baseline, 20 weeks after baseline.
Secondary Outcome Measures
NameTimeMethod
umber of hospital admissions and emergency room visits during study period (1 year or until death of the patient).
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