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Real life experience of quality of life and symptom burden assessment in outpatients with lung and prostate cancer

Real life experience of quality of life and symptom burden assessment in outpatients with lung and prostate cancer - POSPROS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00023195
Enrollment
120
Registered
2020-11-16
Start date
2018-05-01
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

Quality of Life, Distress and Symptom Burden in advanced lung- and prostate cancer C61 C34

Interventions

Group 1: Patients with advanced Lung Cancer received a Distress Thermometer and an IPOS once every four months. During the course of the study the patients, their caregivers and HCP were interviewed i

Sponsors

Interdisziplinäre Abteilung für Palliativmedizin der Universitätsmedizin Mainz
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult patients (at least 18 years old) with CRPC or lung cancer beyond recovery in an advanced state, functionally not operable or without any tumor-specific treatment options and/or UICC IV for NSCLC or extensive disease for SCLC.

Exclusion criteria

Exclusion criteria: Patients underage (under the age of 18 years), insufficient language skills to complete the German questionnaires as well as cognitive or communicative deficits.

Design outcomes

Primary

MeasureTime frame
Scientific monitoring of quality of life and symptom burden measurement with PROMs (Distress Thermometer and IPOS) during the process of becoming a DKG certified CCC.

Secondary

MeasureTime frame
Testing the possibility of measuring quality of life and symptom burden with only one of the two questionnaires used.

Countries

Germany

Contacts

Public ContactEileen Ratzel

Interdisziplinäre Abteilung für Palliativmedizin

eratzel@students.uni-mainz.de0049176-99503707

Outcome results

None listed

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