Evaluation of the treatment concept "AOK proReha"

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00003286

Enrollment

1000

Registered

2012-03-21

Start date

2011-12-01

Completion date

Unknown

Last updated

2025-10-06

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

Conditions

M16 M17

Interventions

Group 1: Patients after hip- or knee TEP are treated according to the treatment concept AOK proReha. Questionnaires are filled out at the beginning of rehabilitation, end of rehabilitation and 6 month

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients after knee- or hip TEP in clinics that participate in the AOK proReha treatment programme.

Exclusion criteria

Exclusion criteria: Patients who cannot fill out german questionnaires due to cognitive or mental health impairements or language problems.

Design outcomes

Primary

Measure	Time frame
Treatment Outcome (e.g. somatic health, pain, functional status, health behavior) with the IRES questionnaire. Points of measurement: Begin of rehabilitation, end of rehabilitation, 6 months after rehabilitation	—

Secondary

Measure	Time frame
patient satisfaction (Patient satisfaction questionnaire developed by the AQMS). Point of measurement: End of rehabilitation	—

Countries

Germany

Contacts

Public ContactJohannes Hauer

Universitätsklinikum Freiburg Abteilung für Qualitätsmanagement und Sozialmedizin (AQMS)

johannes.hauer@uniklinik-freiburg.de0761-27074460

Outcome results

None listed

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