Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05143333 · ClinicalTrials.gov registry record

Cognitive Assessment in COVID-19 Positive Patients Using the DANA App

A clinical trial of COVID-19, sponsored by Johns Hopkins University.

Completed
Registry status
28
Enrollment target
1
Study location

NCT05143333: Completed study of COVID-19, sponsored by Johns Hopkins University.

NCT05143333 is a study of COVID-19 that has completed, run by Johns Hopkins University. The registered enrollment target is 28 participants, below the 38,465-participant average among 298 other COVID-19 trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05143333, a study of COVID-19, has completed, sponsored by Johns Hopkins University.

COMPLETED
Registry status
28 participants
Enrollment target
1
Study location

Study Summary

The Defense Automated Neurobehavioral Assessment (DANA) is a battery of cognitive tests delivered via an electronic tablet or smartphone. The overarching goal of this study is to evaluate the post-acute trajectory of cognitive functioning in patients hospitalized for COVID-19 using the DANA.

Primary Outcome

● Characterize the nature (i.e., pattern of cognitive deficits) and trajectory of cognitive dysfunction among those treated for COVID-19 with high temporal resolution repeatedly for up to 6 months using the DANA.

Conditions Studied

Interventions

  • OTHER DANA app

Study Locations (1)

Maryland

  • Johns Hopkins Psychiatry department - Baltimore

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2021-07-01
Est. Completion 2021-12-31
Johns Hopkins University

1,448 total trials

What the finished NCT05143333 record still lists

NCT05143333 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 38,465-participant average among 298 other COVID-19 trials with a reported enrollment target (100% lower).

The record links to 1 condition, with COVID-19 appearing as the primary indexed condition, and to 1 intervention - of which DANA app is the first listed.

NCT05143333 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT05143333 about?

NCT05143333 is a clinical study titled "Cognitive Assessment in COVID-19 Positive Patients Using the DANA App". The Defense Automated Neurobehavioral Assessment (DANA) is a battery of cognitive tests delivered via an electronic tablet or smartphone. The overarching goal of this study is to evaluate the post-acute trajectory of cognitive functioning in patients hospitalized for COVID-19 using the DANA.

What is the current status of trial NCT05143333?

This trial is currently completed. The enrollment target is 28 participants. The study started on 2021-07-01. Estimated completion is 2021-12-31.

What conditions does trial NCT05143333 study?

This clinical trial studies the following conditions: COVID-19.

What interventions are being tested in trial NCT05143333?

The interventions under investigation include: DANA app (OTHER).

Who is sponsoring clinical trial NCT05143333?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05143333 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for COVID-19

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05143333's enrollment target sits among peer trials

28 272nd of 298 higher than 27 of 298 other COVID-19 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other COVID-19 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03471117 · 28 participants · Phase 4

    Pioglitazone to Reduce Sympathetic Overactivity in CKD Patients

  • NCT03523975 · 28 participants · Phase 1

    Venetoclax, Lenalidomide and Rituximab in Patients With Previously Untreated Mantle Cell Lymphoma

  • NCT03608631 · 28 participants · Phase 1

    iExosomes in Treating Participants With Metastatic Pancreas Cancer With KrasG12D Mutation

  • NCT03810651 · 28 participants · Early Phase 1

    Pencil Beam Scanning in Patients With Renal Tumors

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05143333, the US trial registry maintained by the National Library of Medicine. NCT05143333 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.