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App-based physical intervention training for Long- and Post-COVID treatment

App-based physical intervention training for Long- and Post-COVID treatment - A PILOT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00034476
Enrollment
100
Registered
2025-01-16
Start date
2024-03-04
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

Post-COVID (or post acute sequelae of SARS-CoV-2) U09

Interventions

Group 1: Intervention containing elements of strength and endurance training, relaxation and breathing exercises. The intervention group is introduced to the app during the baseline assessment, throug

Sponsors

Sport- und Rehabilitationsmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: - persistent symptoms (neurocognitive/physical impairments) after SARS-CoV infection - signed declaration of consent and - signed transfer of ownership agreement

Exclusion criteria

Exclusion criteria: Severe end organ damage / cardiac disease with moderately to severely reduced LV function - Concomitant diseases that represent a contraindication for physical activity (e.g. immobilization, serious myopathies) - Limited ability to cooperate (e.g. serious psychiatric and/or neurological illnesses) - Existing pregnancy

Design outcomes

Primary

MeasureTime frame
Primary endpoints are health-related quality of life, cognitive performance, and physical performance (VO2peak). Health-related quality of life is assessed using the German version of the SF-12 (Health Status Questionnaire, Morfeld et al.). According to the questionnaire manual, the core dimensions "Physical Health" and "Mental Health" are determined. Cognitive performance is measured using the Symbol Digit Modalities Test (SDMT, Smith). VO2peak is examined as part of cardiopulmonary performance diagnostics. The primary endpoints are assessed both at the time of the baseline examination and after the eight-week intervention (final examination).

Secondary

MeasureTime frame
Secondary endpoints of the study are: - concentrations of inflammatory markers (IL-1ß, IL-6, TNF-alpha, CRP) - level of Kynurenine, Kynurenic acid, Quinolinic acid (and respective ratios) - echocardiographic parameters (e.g., LV GLS, RV GLS, RV RWS, E/A, E/E'l, E/E'm, etc) - Parameters of Cardio Pulmonary Exercise Testing - Mental health (Severity of depressive symptoms, anxiety and stress) All secondary endpoint parameters are assessed both at the time of the baseline examination and at the final examination (after 8 weeks).

Countries

Germany

Contacts

Public ContactJohannes Kirsten

Sport- und Rehabilitationsmedizin

johannes.kirsten@uniklinik-ulm.de+49 731 50045350

Outcome results

None listed

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