PostCovidCare - Pilot Study on the Implementation of a Post-COVID-19 Case-management with browser-based symptom diary in general practice.
- Conditions
- Post COVID
- Registration Number
- DRKS00029951
- Lead Sponsor
- niversitätsklinikum Heidelberg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 33
Study physician(s) and study VERAH(s) designated to conduct the study in the primary care physician's office.
o Age of majority
o Family practice with participation in the family doctor-centered care in Baden-Württemberg with employment of a VERAH
o Participation in the specified modules of the online basic training on Long-COVID.
For GPs currently participation in at least modules 1 - 3 with knowledge test and participation in module 4 (remedies, respiratory muscle training - self-report) of the basic training Long-/ Post-COVID Registration Online Course - Long-Covid Netzwerk Rhein-Neckar (longcovidnetz.de) is strongly recommended. mandatory for participation in the study is proof of at least one passed knowledge test.
For VERAH currently participation in at least module 1 with knowledge test of the basic training Long- / Post-COVID Registration Online Course - Long-Covid Network Rhine-Neckar (longcovidnetz.de) mandatory.
o Participation in an online training on the study including the use of PostCovidCare (single appointment with 3 UE à 45min) (VERAH and ARZT/ÄRZTIN).
o Written consent to participate in the study.
o EDP requirements and willingness to use the CareCockpit software by MFA/VERAH available
o EDP requirements and readiness for the use of the CareCockpit software by the DOCTOR during the consultation are fulfilled.
o The inclusion criteria are checked by the Department of General Medicine and Health Services Research.
- Patients
o Capacity to give consent given
o Age = 18 years
o Diagnosis U09.9! set
o Indication of disorders/symptoms classified elsewhere that led to the diagnosis of post-COVID syndrome and are relevant to treatment (at least 1 disorder/symptom in ICD-10 must be indicated).
o positive SARS-CoV-2-PCR detection at least 4 weeks ago
or
o as of 01.06.2022 positive antigen rapid test from official test center (= with certificate according to § 6 paragraph 1 Coronavirus Test Ordinance (for example at the testing center, pharmacy, general practitioner's office))
o Patient suitability
PC or mobile device with internet access
Willingness to use a browser-based symptom diary
o Written consent after medical consultation
- General practitioners
o Practice location outside of Baden-Württemberg
o No willingness to integrate the browser-based symptom diary
- Patients
o sole proof of COVID-19 disease by positive nucleocapsid antibodies
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main target criteria of the pilot study are the survey of <br>- Usability (usability) quantitatively by means of System Usability Scale (SUS); User Experience Questionnaire (UEQ) <br>- Implementation quantitatively by means of questionnaires oriented to the RE-AIM-Framework<br>- Supplementary collection of qualitative data on usability and implementation by means of accompanying semi-structured interviews (oriented on the RE-AIM framework)<br>- potential effectiveness on <br>o from patients' perspective perceived satisfaction with GP medical care by means of PACIC-S5 questionnaire <br>o from primary data: Type and number of diagnostic and therapeutic interventions performed.
- Secondary Outcome Measures
Name Time Method