Effectiveness of an interdisciplinary rehabilitation treatment for patients with post-COVID syndrome who perceive high levels of disabilities - Single Case Experimental Design Study

Effectiveness of an interdisciplinary rehabilitation treatment for patients with post-COVID syndrome who perceive high levels of disabilities - Single Case Experimental Design Study - Effect of an interdisciplinary rehabilitation treatment for post-COVID

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON53306

Enrollment

Registered

2023-07-18

Start date

2023-09-25

Completion date

Unknown

Last updated

2025-09-08

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

Conditions

long lasting corona complaints post-covid

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: To be eligible for participation in this study, patients must meet all the following criteria: - COVID-19 symptoms persisting for more than 12 weeks after initial infection - Experiencing high levels of disability in daily activities and/or participation due to PCS (rehabilitation physician based). - Indicated for an interdisciplinary rehabilitation treatment in secondary care (as decided by a rehabilitation physician). - Good command of written and spoken Dutch - Having access to the Internet - >= 18 years.

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: - Illiteracy / no good knowledge of Dutch - No access to a smartphone, tablet or computer (or insufficient digital skills) - Experiencing high levels of disability in daily activities and/or participation before their COVID- 19 infection

Design outcomes

Primary

Measure	Time frame
Primary outcome of the study will be participation in society (USER-P) and health-related quality of life (EQ5D-5L).	—

Secondary

Measure	Time frame
Secondary outcomes will be daily diary items and validated questionnaires aimed at physical, mental and cognitive complaints, healthcare- and social costs and feasibility of the treatment.	—

Countries

Netherlands

Outcome results