Post COVID

2

Review clinical trials related to Post COVID. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

sElective Serotonin reuPtake inhibitoRs In posT-covid After COVID-19

Fatigue, cognitive problems, post-exertional malaise (PEM) and postural orthostatic tachycardia syndrome (POTS) are common and debilitating symptoms after COVID-19. The pathophysiology of post-COVID is not well understood and there is no established biomedical treatment. Treatment options for post-COVID are thus much needed. A promising candidate intervention is fluvoxamine, a selective serotonin reuptake inhibitor (SSRI), that may reduce post-COVID symptoms because of its regulatory effect on the (neuro) immune system, the hypothalamic-pituitary-adrenal (HPA) axis and the tryptophan system. The investigators will randomize 160 participants to either fluvoxamine or placebo for 12 weeks. The investigators will use advanced functional neuroimaging techniques during cognitive challenge (optional substudy) and plasma biomarkers (inflammatory markers, cortisol, serotonin, IDO-2 activity), to facilitate identifying potential mechanistic pathways of post -COVID treatment.

Participants needed: 160
Trial details
Phase: Phase 3Age: 18-70Biological sex: AllType: InterventionalSponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)Updated: Jun 9, 2026Locations: 1
Eligibility criteria

Adults aged 18 to 70 years [+8]

Use of medication with interaction with fluvoxamine that cannot be discontinued [+16]

Status: Recruiting

ACT for Mental Health in Neurological Disorders

The goal of this clinical trial is to examine the efficacy of this manual for mental health in people with mixed neurological disorders, including post-COVID. These conditions are often associated with cognitive impairment, which may hamper the effects of psychoterapy. Executive functioning and especially the ability to abstract thinking may be useful for individuals using Acceptance and Commitment Therapy. Therefore, the main questions research questions are: * Is this intervention effective in improving mental health? * Do executive functions predict the extent of social participation and mental health at the end of therapy? Participants will take part in 8 weekly group therapy sessions of 100 minutes each.

Participants needed: 44
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Bielefeld UniversityUpdated: Mar 27, 2025Locations: 1
Eligibility criteria

Value above a cut-off of the DASS-21 subscales (depression > 10, anxiety > 6, an... [+2]

Behavioral disorders (e.g., high irritability or apathy in clinical rating) [+2]