Patient-reported outcomes in the treatment of oncological patients - A multicentred pilot study to select appropriate assessment instruments

Patient-reported outcomes in the treatment of oncological patients - A multicentred pilot study to select appropriate assessment instruments - PRO-ONKO

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00005337

Enrollment

100

Registered

2013-11-28

Start date

2014-01-02

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

C00-D48

Interventions

Group 1: Cancer patients, aged >18 Years, heterogenious diagnoses, undergoing in and/ or out-patient treatment complete questionnaires to assess patient reported outcomes(PRO) and evaluate their usefu

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Cancer patients, aged >18 Years, heterogenious diagnoses, undergoing in and/ or out-patient treatment who gave written informed consent.

Exclusion criteria

Exclusion criteria: non-sufficient understanding of the German language, cognitive impairments (e.g. dementia) or not able to give informed consent.

Design outcomes

Primary

Measure	Time frame
A modular assessment tool that fulfils the requirements of both patients and practitioners to facilitate supportive therapy and symptom management of oncologic patients.	—

Countries

Germany

Contacts

Public ContactHeike Schmidt

Institut für Gesundheits- und Pflegewissenschaft, Medizinische Fakultät der Martin-Luther-Universität, Halle-Wittenberg

heike.schmidt@medizin.uni-halle.de+49 345 5574194

Outcome results

None listed

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