Study identity card

InvidiCO

Germany
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  • Disease: Post-COVID-19
  • Study type: Randomised Clinical Trial
  • Study type descriptors: Interventional
  • Study aim: To evaluate the effectiveness of the unguided digital therapeutic vimida in reducing post-COVID-19 fatigue
  • Number of participants enrolled: Enrollment ongoing
  • Study enrolling from to
  • Study includes follow-up for 6 months

Study Data

  • Adults
  • Elderly
  • General population
  • SARS-CoV-2
  • Post-COVID-19
  • Non pharmacological intervention
  • Vimida
  • Rehabilitation

Other information

Funders:

  • Gaia AG

If you would like to contact the Principal Investigator of the study please email: ccb@ateneo.univr.it

The data is updated up to