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Teleconsultation for patients with postviral symptoms

Patient-centred interprofessional teleconsultation for patients with postviral symptom complexes (Subproject of, "Coordinated LongCOVID care system for integrated supply and capacity expansion in Mecklenburg-Western Pomerania (COVI-Care M-V)")

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11050086
Enrollment
240
Registered
2025-04-28
Start date
2026-04-01
Completion date
Unknown
Last updated
2025-09-22

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

Conditions

Long- and post-COVID and other post-viral symptom complexs Infections and Infestations

Interventions

Interprofessional, patient-centred teleconsultation initiated and supervised by the GP with the patient and GP at one end (GP practice) and Long-COVID specialists from Rostock University Medical Cente

Sponsors

Bundesverwaltungsamt
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients: 1. Presence of a post-viral symptom complex 2. Age from at least 18 years Physicians: 1. General practitioners based in Mecklenburg-Western Pomerania (Germany)

Exclusion criteria

Exclusion criteria: Patient exclusion criteria: 1. Presence of an acute underlying malignant disease 2. Remaining life expectancy of less than 12 months as assessed by a GP 3. Language barriers (e.g. hearing impairment, lack of language skills) 4. Dementia and lack of capacity to give consent

Design outcomes

Primary

MeasureTime frame
Physical performance measured using the target and actual value of the walking distance of the 6-minute walk test between patient inclusion (T0) and 4 months later (T1)

Secondary

MeasureTime frame
The following secondary outcome measures are assessed before the intervention (T0) and four months later (T1): 1. Health-related quality of life measured using the Post Acute COVID-19 Quality of Life (PAC-19QoL) tool 2. Cognitive impairment measured using the DemTect screening test 3. Lung performance measured using a peak flow meter 4. Symptoms of fatigue measured using the Fatigue Assessment Scale (FAS)

Countries

Germany

Contacts

Public ContactChristin Löffler
christin.loeffler@med.uni-rostock.de+49 381 494 2481

Outcome results

None listed

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