Development of Voice Biomarkers of Frequent COVID-19 and Long Covid-related Symptoms Based on Data From Users of the Long COVID Companion App

ConditionLong COVID
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorLuxembourg Institute of Health

About this trial

The LIH DDP research team focuses its research topics on vocal biomarkers and Long COVID, among others. Voice is indeed a promising tool to monitor health, as it contains many information on our health and is easy to collect.

The development of vocal biomarkers of Long COVID-related symptoms could improve the remote monitoring of the health status of people affected by this disease.

The LIH developed the Long COVID Companion (LCC) app in collaboration with the ApresJ20 Long COVID patient association in France to support patients in their daily lives. LCC app users will be invited to participate in this study to collect voice recordings at the same time as health-related data.

The objectives of this study are:

Primary objective: To develop vocal biomarker candidates for the main Long COVID symptoms (fatigue, brain fog, respiratory problems, sleep issues, stress, anxiety,..) in a population of people with Long COVID.

Secondary objectives:

* to assess the intra-individual longitudinal evolution of voice characteristics of people with LC * to assess app usability and acceptability in the long-term.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult (≥18 years old)

Male or female

People with persisting symptoms related to COVID-19 (With Long COVID diagnosis or not)

Adequate understanding of one of the study languages (English, French, German)

Disqualifiers

None

Trial population

All adult people with suspected Long COVID can participate in this study. As the study is completely digital, there are no restriction in terms of living country. All the users of the Long COVID Companion app will be invited to participate in the study (by email or directly in the app). Recruitment will also be done by communications on social media, and by distributing study flyers in the waiting rooms of Long COVID consultations network. Participants to the PrediCOVID study who accepted to be recontacted will also be invited. Information regarding the study will also be disseminated to all people with Long COVID in the database of the Long COVID consultation network in Luxembourg.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • No Intervention: Observational Cohort

    Other intervention

    Participants will be followed digitally using the LCC app. They will complete questionnaires about their health status and do voice recordings on their own rhythm during the entire study duration.

Treatment groups

300 Participants
are divided into 1 treatment group
Group A: Long Covid Companion (LCC) app users1 intervention

Trial outcomes

Primary outcomes

1

Fatigue level

Level of fatigue will be assessed regularly using a 0-5 likert scale. Participants will complete these questionnaires when they want during the follow-up.

Time frame
From enrollment until 24 months after
2

Fatigue level

Level of fatigue will be assessed regularly using FSS9 questionnaire. Participants will complete these questionnaires when they want during the follow-up.

Time frame
From enrollment until 24 months after
3

Voice features

* Source features (e.g., jitter, shimmer) reflecting the origin of voice production * Formant features (e.g., F1, F2, F3 frequencies, bandwidths) representing resonant frequencies of vocal and nasal tracts * Spectral features (e.g., centroid, MFCCs, flatness) capturing frequency distribution at specific moments * Prosody features (e.g., pitch, intensity, speech rate, pause duration) describing rhythm and intonation

Time frame
From inclusion until 24 months after

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: