Study identity card

BEACON

United Kingdom
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  • Disease: Post-COVID-19
  • Study type: Randomised Clinical Trial
  • Study type descriptors: Interventional, Single centre
  • Study aim: To establish the effectiveness and cost-effectiveness of the ReaCT brain training program in adults with cognitive impairment following COVID-19
  • Number of participants enrolled: 32
  • Study enrolling from to
  • Study includes follow-up for 6 months

Study Data

  • General population
  • Elderly
  • Adult
  • Primary care
  • SARS-CoV-2
  • Post-COVID-19
  • Non pharmacological intervention
  • Rehabilitation

Other information

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

The data is updated up to