Actively Recruiting

Age: 18Years +
All Genders
NCT04586413

Post Acute COVID-19 Quality of Life (PAC-19QoL) Tool Development and Patient Registry (PAC-19QoLReg)

Led by Medialis Ltd. · Updated on 2023-10-23

100

Participants Needed

1

Research Sites

416 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Coronavirus Disease 2019 (COVID-19) is a newly emerged disease, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The COVID-19 pandemic is having a large impact on the mental and physical health of patients, yet data on the quality of life of post-COVID-19 patients is lacking. There are currently no post-COVID-19 specific measures for quality of life, particularly none which include the views of post-COVID-19 patients themselves. This observational study will recruit participants to contribute their preferences to the creation of a post-COVID-19 specific patient-reported measure on post-COVID-19 quality of life. Participants will be split into three groups: those who were not hospitalised; those who were hospitalised but not in intensive care units; and those who were hospitalised and in intensive care units. The creation of this measure will form phase 1 of the study, with 30-60 participants (10-20 in each group above) recruited to complete online surveys to find out their preferences of areas of life to include in such a measure. This will involve 3 online surveys, 1) to ask which areas of life they feel are impacted and how; 2) to find consensus about the areas to be included; 3) to weight the relevance of these areas in relation to each other. In phase 2 recruitment will open to additional participants and all participants will be asked to complete the finalised post-COVID-19 quality of life measure once a month for 12 months, aiming for a minimum of 100 participants at this stage. All participants will also be asked to complete a demographic questionnaire to inform the analysis of the data.

CONDITIONS

Official Title

Post Acute COVID-19 Quality of Life (PAC-19QoL) Tool Development and Patient Registry (PAC-19QoLReg)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • The participant has had either a confirmed COVID-19 test while infected or a confirmed COVID-19 antibody test post-infection (Phase One) or a confirmed COVID-19 test, antibody test, or clinical diagnosis of COVID-19 (Phase Two)
  • The participant is aged 18 years or older
  • The participant is capable of providing informed consent
  • The participant can read, write and converse in English
  • The participant can comply with the study schedule
Not Eligible

You will not qualify if you...

  • The participant does not have a confirmed COVID-19 test, antibody test, or clinical diagnosis of COVID-19
  • The participant is aged under 18 years
  • The participant is not capable of giving informed consent
  • The participant is unable to read, write and converse in English
  • The participant is unable to comply with study schedule data collection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medialis

Oxford, United Kingdom, OX16 0AH

Actively Recruiting

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Research Team

O

Omolade Femi-Ajao, PhD

CONTACT

R

Ravi Jandhyala

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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