ClinicalTrials.gg
Status unknownNCT05545332PRECISEUpdated Sep 19, 2022

Prospective Multidisciplinary Post-COVID-19 Registry Tyrol

An observational study in Post COVID-19 Condition, sponsored by Medical University Innsbruck. Status unknown at 1 site in Austria. Per ClinicalTrials.gov, last updated 2022-09-19.

Sponsored by Medical University Innsbruck · Observational

The sponsor has not verified this record recently (last verified Aug 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
600
Sex
All
01

Study summary

Longitudinal, prospective observational cohort study enrolling patients with persisting symptoms (> 12 weeks) after COVID-19 in a multidisciplinary care model.

Read the detailed description

Post-COVID-19 syndrome comprises a set of persistent physical, cognitive and/or psychological symptoms that continue for more than 12 weeks after illness and are not attributable to alternative diagnoses. As these symptoms may manifest in all COVID-19 severity grades, even in patients with mild or moderate disease, there is an urgent need for resource allocation in the health care system and accompanied research proposals to understand disease phenotypes and clinical trajectories.

With this prospective multidisciplinary registry, the investigators aim to establish a clinical and researchbased system by providing optimized medical diagnostic and therapeutic approaches in a model region in Austria (Tyrol).

02

Conditions studied

  • Post COVID-19 Condition

Keywords

  • post COVID-19 syndrom
  • long COVID
  • long term sequelae
03

In context

Post-Acute COVID-19 Syndrome

536 studies on the registry are indexed under Post-Acute COVID-19 Syndrome; 187 are open to participants now.

This study's planned enrollment of 600 is above the median of 160 across 149 observational studies indexed under Post-Acute COVID-19 Syndrome.

Browse Post-Acute COVID-19 Syndrome studies →

Lead sponsor

Medical University Innsbruck is the lead sponsor of 186 studies on the registry; 48 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Eligible patients will be screened by primary physicians in Tyrol (Wester Austria) using the post-COVID-19 functional status (PCFS) scale to assess the functional status, and a symptom checklist for the presence and severity of the 10 most common symptoms.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Individuals with persistent post COVID symptoms ≥ 12 weeks
  • post COVID functional status scale (PCFS) ≥ 2

Exclusion criteria

Exclusion Criteria:

  • observation time after infection \< 12 weeks
  • PCFS \< 2
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
600 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Prevalence rates of post-COVID patients requiring multidisciplinary care.

    To quantify disease burden by prevalence rates of post-COVID patients requiring multidisciplinary care.

    Time frame: 2 years

  2. Characterisation of symptom patterns associated with impaired functional status.

    Characterisation of symptom patterns associated with impaired post covid-19 functional status scale ≥ 2.

    Time frame: up to 24 months

07

Study locations

1 of 1 sites recruiting
  • Medical University of Innsbruck
    Innsbruck, 6020, Austria
    • Judith Löffler-Ragg, Prof. Dr. · Contact
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — We provide all of the individual participant data collected during the trial after deidentification and to researchers who provide a methodologically sound proposal.

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Analytic code

Time frame: Beginning three months after publication and ending five years following article publication.

Access criteria: Access to researchers who provide a methodologically sound proposal.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 19, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05545332
Responsible party
Sponsor
First posted
Sep 19, 2022
Start date
Mar 3, 2022
Primary completion
Dec 31, 2023 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Sep 19, 2022

Study contacts

Judith M Löffler-Ragg
Contact
judith.loeffler@i-med.ac.at
+43 512 504 ext. 81413

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion