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Outpatient respiratory therapy for patients with post-COVID-19 syndrome - A feasibility study

Outpatient respiratory therapy for patients with post-COVID-19 syndrome - A feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00029206
Enrollment
30
Registered
2022-06-17
Start date
2022-06-23
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

ICD.10 U09.9G: Post-COVID-19 condition, unspecified.

Interventions

Group 1: Patients with post-COVID syndrome: observation of physiotherapeutic breathing therapy over a period of nine weeks. Before and after the observation period, physiotherapeutic respiratory fin

Sponsors

Universitätsklinikum Heidelberg Abteilung Allgemeinmedizin und Versorgungsforschung
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients: Personal consent to participate in the study, good knowledge of German, onset of symptoms of COVID-19 disease more than twelve weeks ago, physician's prescription for physiotherapy with the diagnosis U09.9, persistent symptoms of post-COVID syndrome (primarily shortness of breath / problems with breathing). Physical Therapists: State-recognized professional title of physiotherapist, personal consent to participate in the study, good knowledge of German, work as a physiotherapist in an outpatient setting (practices/rehabilitation centers), participation in the online information event to introduce the study and the study measures before study inclusion.

Exclusion criteria

Exclusion criteria: Patients: Poor general health (which does not allow for outpatient treatment), need for home visits, limitations (which do not allow the patient to complete the questionnaires independently, such as dementia), severe lung disease (such as COPD), severe mental illness. Physical Therapists: Physical therapists who have had their professional title revoked and/or are unauthorized to use it.

Design outcomes

Primary

MeasureTime frame
- recruitment (after completion of recruitment: qualitative survey by means of questionnaire and semi-structured interview). - compliance (after application of the study documents: qualitative survey by means of questionnaire and semi-structured interview, quantitative survey by means of actual documentation on the documentation forms) - potential effectiveness (after completion of the study: quantitative survey by means of documentation on the findings sheets and the questionnaires on fatique, dyspnea, activity and participation, and quality of life)

Secondary

MeasureTime frame
- respiratory therapy content - safety of study content - factors influencing access to care and respiratory therapy feasibility

Countries

Germany

Contacts

Public ContactMarie Hencke

Universitätsklinikum Heidelberg Abteilung Allgemeinmedizin und Versorgungsforschung

marie.hencke@stud.uni-heidelberg.de015733665260

Outcome results

None listed

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