Skip to content

Evaluation study of subproject 1 MOVE-COVID-BW (COVID 19)

Evaluation study of subproject 1 MOVE-COVID-BW (COVID 19)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033028
Enrollment
65
Registered
2024-05-07
Start date
2024-05-08
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

Long-COVID: Evaluation of the quality of care in special outpatient clinics

Interventions

Group 1: The evaluation study of sub-project 1 (MOVE-COVID-VF) of the MOVE-COVID-BW research project is a participatory research project in which the parents of children with Long COVID (LC) and servi

Sponsors

Universitätsklinikum Freiburg
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Only people who have agreed to the MOVE-COVID-VF informed consent form will be included in the study. Inclusion criteria for participation in the study are sufficient knowledge of the German language so that the questionnaires can be completed and an exchange in the context of qualitative interviews is possible. Participation in the interviews with socially disadvantaged parents is only possible if they take part in the questionnaire survey and are invited to an interview at the end of the questionnaire by calculating their social status. Only families with a confirmed diagnosis are included.

Exclusion criteria

Exclusion criteria: not applicable

Design outcomes

Primary

MeasureTime frame
No primary or secondary outcome measures are formally defined in the evaluation study, as it is not an intervention study. When analyzing the quality of results, the focus is on the perceived quality of care from the perspective of parents and service providers.

Secondary

MeasureTime frame
see above

Countries

Germany

Contacts

Public ContactThorsten Langer

Universitätsklinikum Freiburg

thorsten.langer@uniklinik-freiburg.de+49 761 270-43442

Outcome results

None listed

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