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Symptom trajectories in patients with advanced chronic obstructive pulmonary disease (COPD) or lung cancer - a prospective longitudinal study

Symptom trajectories in patients with advanced chronic obstructive pulmonary disease (COPD) or lung cancer - a prospective longitudinal study - SYMPATIE study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00000312
Enrollment
100
Registered
2010-07-15
Start date
2010-02-10
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

J44 C34

Interventions

None listed

Sponsors

Institut für Palliative Care (ipac) e.V.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with the following criteria will be eligible for this study. The inclusion criteria will be: 1)diagnosis of advanced disease as defined as follows: Lung cancer: Primary lung cancer at all stages (small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC)), cancer at any site with secondary tumour of the lung (lung metastasis); COPD: stage III or IV of the GOLD classification (Global Initiative for Obstructive Lung Disease), which include the airflow limitation measured by spirometry FEV1 < 50%, FEV1/FVC < 0.7 (FEV1: forced expiratory volume in one second; FVC: forced vital capacity) and symptoms such as more severe breathlessness, reduced exercise capacity and repeated exacerbations; 2)age = 18 years. Disease orientated therapies (chemotherapy, radiotherapy, surgery) can be ongoing.

Exclusion criteria

Exclusion criteria: (1) lack of capacity to give informant consent; (2) lack of capacity to be interviewed;(3)cognitive impairment (clinical judgment by the principal investigator)

Design outcomes

Secondary

MeasureTime frame
symptoms and needs: Palliative Care Outcome Scale (POS); functional ability: Karnofsky Performance Scale (KPS); quality of life: EuroQoL5 (EQ-5D); health service use: number of hospital admissions, number of admissions to A&E; comorbidities: Charlson Comorbidity Index (CCI)

Primary

MeasureTime frame
Dyspnoea: modified Borg-Scale; episodic breathlessness: number of attacks, mean length of attack, severity of attack Time of measurement: every 4 weeks

Countries

Germany

Contacts

Public ContactSteffen Simon

Institut für Palliative Care (ipac) e.V.

steffen@steffensimon.de0049-(0)441-9984324

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026