Disease × agent evidence record

Digital Cognitive Behavioral Intervention-Rxwell for Long COVID: evidence, trials and status

Trials of Digital Cognitive Behavioral Intervention-Rxwell in Long COVID are registered but none has completed, so there is no outcome evidence from those studies yet; the record is a signal of research interest.

1 registered trials 0 recruiting 0 publications Evidence tier B · Moderate Score 12.5
Research Tracker › Pairs › Long COVID › Digital Cognitive Behavioral Intervention-Rxwell
Research map, not treatment advice. This page aggregates registry and literature records. It does not evaluate efficacy, dosing or safety for any individual. Discuss any treatment decision with a qualified clinician.

Summary

Digital Cognitive Behavioral Intervention-Rxwell is tracked by OSMF as an investigational option for Long COVID; no regulator has approved it for this indication, and most post-viral conditions have no approved disease-modifying therapy at all. ClinicalTrials.gov lists 1 registered trial linking Digital Cognitive Behavioral Intervention-Rxwell to Long COVID: 1 is terminated, withdrawn, suspended or of unknown status. The most advanced is Phase 4 (NCT05597722, sponsored by Eva Szigethy). It plans or enrolled 7 participants. Registered activity dates to 2023. No published literature item is linked to Digital Cognitive Behavioral Intervention-Rxwell and Long COVID in the OSMF database yet, so the record rests on registry entries alone. Registry entries describe intent to study, not outcomes.

Long COVID / PASC is tracked on the OSMF post-viral programme alongside ME/CFS, Long COVID, POTS and MCAS. Across the programme, 423 candidate agents are logged for Long COVID, most of them preliminary; this page isolates the record for one of them.

Evidence table

Evidence tierB · Moderate
Evidence score12.5 (trials 2.5, literature 0.0, tier 10, approved bonus 0.0)
Registered trials1 total: 0 recruiting, 0 active / not yet recruiting, 0 completed, 1 other
Linked publications0
Agent typeBehavioural (Behavioral / Protocol / Exercise)
Development stage (any indication)Investigational
Mechanism / classNeurological / Autonomic
Data sourcesOSMF therapeutic agent database, ClinicalTrials.gov
How the evidence score is calculated
  • Each registered trial scores by status (recruiting / active / enrolling 3, completed 2.5, not yet recruiting 2, unknown 1, terminated / withdrawn / suspended 0.5) plus a phase bonus (phase 3-4 +2, phase 2 +1, phase 1 +0.5). The trial component is capped at 30.
  • Each literature item scores by design (Cochrane review 5, meta-analysis 4, systematic review 3, RCT 3, clinical trial publication 2, curated reference 1.5, other PubMed record 1). The literature component is capped at 30.
  • The existing evidence tier adds 15 (A / Strong), 10 (B / Moderate), 5 (C / Preliminary) or 0 (D / Anecdotal).
  • Agents approved for any indication (max clinical phase 4) add 5, because an approved agent has an established safety profile that lowers the barrier to repurposing trials.
  • The score ranks what has been studied, not what works. It does not read effect sizes or directions of effect.

Registered clinical trials

NCT IDTitleStatusPhaseEnrolment
NCT05597722Addressing Cognitive Fog in Long-COVID-19 Patients
Eva Szigethy · 2023
terminatedPhase 47

Search ClinicalTrials.gov for newer studies

Published literature

No publication is linked to this pair yet.

Run the live PubMed search

Mechanism and notes

Recorded mechanism or class: Neurological / Autonomic.

Clinical notes: Investigational for listed conditions. 1 associated trial(s) and 0 study reference(s) in current data. Review primary sources and consult specialists before use.

Safety: Limited specific safety data in these populations. Review full prescribing information and consult specialist. Many agents used off-label or investigational.

Dosing in studies: See linked studies/trials for reported doses and durations; typical protocols vary widely.

Frequently asked questions

Is Digital Cognitive Behavioral Intervention-Rxwell approved for Long COVID?

Digital Cognitive Behavioral Intervention-Rxwell is tracked by OSMF as an investigational option for Long COVID; no regulator has approved it for this indication, and most post-viral conditions have no approved disease-modifying therapy at all. Approval status for the specific indication should always be confirmed with the relevant regulator and prescribing information.

Is Digital Cognitive Behavioral Intervention-Rxwell in clinical trials for Long COVID?

ClinicalTrials.gov lists 1 registered trial linking Digital Cognitive Behavioral Intervention-Rxwell to Long COVID: 1 is terminated, withdrawn, suspended or of unknown status. The most advanced is Phase 4 (NCT05597722, sponsored by Eva Szigethy). It plans or enrolled 7 participants. Registered activity dates to 2023.

What does the evidence show for Digital Cognitive Behavioral Intervention-Rxwell in Long COVID?

Trials of Digital Cognitive Behavioral Intervention-Rxwell in Long COVID are registered but none has completed, so there is no outcome evidence from those studies yet; the record is a signal of research interest. OSMF's existing evidence tier for this pair is B (Moderate), taken from the OSMF therapeutic agent database, which grades agents by the volume and design of condition-specific evidence rather than by effect size.

Cite this page

Open Source Medicine Foundation. Digital Cognitive Behavioral Intervention-Rxwell for Long COVID: evidence, trials and status. OSMF Research Tracker. Updated 2026-10-07. https://research.opensourcemed.info/pairs/long-covid/digital-cognitive-behavioral-intervention-rxwell.html

Data: ClinicalTrials.gov, PubMed, Open Targets, ChEMBL, DGIdb and the OSMF therapeutic agent database. Last updated 2026-10-07. Page built 2026-10-07.

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This is a research map, not treatment advice. Evidence tiers and scores summarise what has been studied, not whether a treatment works or is safe for you.