Prevention of Long Covid Syndrome
CompletedNot applicableNCT05793736
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Biofeedback equipment is classified by the Food and Drug Administration (FDA) as medical device class II and this type of equipment/treatment has shown evidence regarding stress management in post-Covid-19 syndrome. The main objective of the study is to verify the feasibility of an HVR biofeedback training protocol in patients with long covid, and also to verify improvement induced by the technique in relation to: cognitive performance; pain perception; fatigue; quality of life; depressive and anxious symptoms
Study details
- Official title
- A Feasibility Study of an HVR Protocol Biofeedback Training to Manage Long Covid Syndrome Symptoms
- Conditions
- Post-Acute COVID-19 Syndrome
- Biofeedback, Psychology
- Quality of Life
- Depressive Symptoms
- Fatigue
- Anxiety
- Pain
- Cognitive Symptom
- Interventions
- Device: Biofeedback training
- Drug: Treatment as usual
- Sponsor
- University of Cagliari
- Start date
- 2023-02-02
- Primary completion
- 2023-10-30
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- Italy
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * People who have contracted Covid-19 and have symptoms attributable to Long syndrome Exclusion Criteria: * patients with cognitive difficulties and/or diagnosis of mental retardation * patients with severe comorbidities with the exception of anxious/depression symptoms arising in conjunction with the viral infection or long covid syndrome.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05793736