U09.9 U07.1
Conditions
Interventions
Group 1: live-online Occupational Therapy
Group 2: Video-Occupational Therapy
Group 3: Waiting list control group
Sponsors
Medizinische Hochschule Hannover
Eligibility
Sex/Gender
All
Age
16 Years to No maximum
Inclusion criteria
Inclusion criteria: Cognitive symptoms consistent with Long COVID disease and persisting for at least four weeks after PCR-confirmed infection with SARS-CoV-2, Access to a technical medium (e.g., PC, tablet with internet access) that can be used to participate in one of the digital intervention options, Consent of the participant or legal guardian.
Exclusion criteria
Exclusion criteria: Age under 16 years diagnosed cognitive impairment prior to infection with SARS-CoV-2 or in the context of another diagnosed underlying disease, previous SARS-CoV-2 was not confirmed by PCR test, No access to PC, tablet, smartphone with internet access, No informed consent to participate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Feasibility (pilot study) | — |
Secondary
| Measure | Time frame |
|---|---|
| Ability to concentrate memorization health-related quality of life cognitive function social participation Activity performance and satisfaction | — |
Countries
Germany
Contacts
Public ContactChristine Happle
Klinik für pädiatrische Pneumonologie, Allergologie, und Neoantologie, Medizinische Hochschule Hannover
Outcome results
None listed