Skip to content

Changes of spirometric data in the 6-MWT due to an outpatient PR in COPD patients: a controlled trial

Changes of spirometric data in the 6-MWT due to an outpatient PR in COPD patients: a controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00009759
Enrollment
30
Registered
2015-12-10
Start date
2015-12-01
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

chronic obstructive pulmonary disease J44.9

Interventions

Group 1: COPD Patient stage II - IV take part at an outpatient rehabilitation Program at the Medical Clinic and the outpatient pulmonary Rehablilitation Center at Leverkusen (Training Group). At the

Sponsors

St. Remigius Krankenhaus
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 90 Years

Inclusion criteria

Inclusion criteria: COPD stage II-IV in a stable condition, maximum 2 weeks to the last exacerbation, written consent, ability to walk

Exclusion criteria

Exclusion criteria: Oxygen dependency, lost mobility, diagnosis making it impossible to complete the rehab program, no written consent

Design outcomes

Primary

MeasureTime frame
spirmetric mesasured inspiratory capacity, before and three weeks later, after the rehabilitation.

Secondary

MeasureTime frame
Maximum Minute volumne, breathing frequency, Walking distance in the 6 Minute Walking test, Oxygensaturation measured during the 6-MWT, usability questionere (7 Points lickert scale); before the rehabilitation program and three weeks later, at its end.

Countries

Germany

Contacts

Public ContactMarc Spielmanns

St. Remigius Krankenhaus

spielmanns@k-plus.de02171 409 2351

Outcome results

None listed

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