COVID-19: Predictors, clinical course and long-term outcome

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00025606

Enrollment

120

Registered

2021-06-21

Start date

2020-06-02

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

U07.1

Interventions

Group 1: Five study visits will be conducted per patient. Visits 1 (at study inclusion) and visits 2 (at discharge from rehabilitation) consist of questionnaires and assessments regarding fatigue (Fat

mMRC dyspnoea scale), health-related quality of life (EQ-5D-5L), pain and sensory impairments (visual analogue scale, descriptive) and olfactory function (sniffin´ sticks). Additionally, information a

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: laboratory-confirmed COVID-19 disease, after the infectious stage (after two negative PCR-tests), being discharged from intensive care unit.

Exclusion criteria

Exclusion criteria: Insufficient communication skills which would interfere with the accomplishment of the questionnaires and assessments, patients in palliative care.

Design outcomes

Primary

Measure	Time frame
Description of the clinical course and of the long-term outcome regarding motor function, activity and participation, lasting symptoms, mental health.	—

Secondary

Measure	Time frame
Definition of predictors for a favorable health state at clinical discharge and 3,6 and 12 months after discharge.	—

Countries

Germany

Contacts

Public ContactMarion Egger

Schön Klinik Bad Aibling Harthausen

megger@schoen-klinik.de08061 / 903 1954

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 9, 2026