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SchizophreniaOBSERVSPEECHNCT06613334

Voice-Based Biomarkers: A Novel Approach to Monitoring and Predicting Schizophrenia Relapses

A study testing Blood test: measurement of plasma antipsychotic concentration and Voice interviews and questionnaires carried out via the CALLYOPE application in people with Schizophrenia, run by Centre Hospitalier St Anne at 2 sites in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Schizophrenia is a serious psychiatric illness affecting approximately 25 million people worldwide. Patients with schizophrenia experience hallucinations, auditory illusions, disordered thinking, movement disorders, cognitive impairment and social isolation. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Schizophrenia
What is being tested?
Blood test: measurement of plasma antipsychotic concentration and Voice interviews and questionnaires carried out via the CALLYOPE application
Could I receive a placebo?
No, everyone receives an active treatment
How many people
200 participants
Where
2 sitesFrance
Study dates
4 Oct 2024to Oct 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Affiliated to a social security or other social protection scheme
  • Diagnosed with schizophrenia according to the DSM-5 (code F20)
  • Stable state without duration criteria
  • Main treatment with risperidone or paliperidone, aripiprazole, olanzapine in oral or long-acting injectable form
  • Complementary treatment with an antipsychotic for anxiolytic or sedative purposes: chlorpromazine, loxapine or cyamemazine
  • Able to speak and read French
Show all 10Show fewer
  • Able to perform speech evaluations
  • Able to answer questionnaires on smartphone
  • May be under curatorship or guardianship
  • Agreeing to participate in the study and with informed consent signed by the subject, as well as by the legal representative in the case of a person under curatorship or guardianship

Who cannot join

  • Suffering from a pathology that impairs French
  • Suffering from a neurological pathology: multiple sclerosis, Parkinson's disease, Huntington's disease or neurodegenerative disease
  • Treatment with lithium salts
  • Anti-epileptic treatment
  • Participant in another study involving medication

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

France2 sites, 2 recruiting
  • Groupe Hospitalo-Universitaire Paris Psychiatrie et Neurosciences, Paris

    Paris, Paris, 75014

    Pierre De Maricourt, Dr, +33145658941, P.DEMARICOURT@ghu-paris.fr

    Recruiting
  • Groupe Hospitalo-Universitaire Paris Psychiatrie & Neurosciences

    Paris, 75014

    Pierre De Maricourt, Dr, 01 45 65 86 91 ext. +33, P.DEMARICOURT@ghu-paris.fr

    Not yet recruiting

Other trials in France

About this study

Official title: Automatic Measurement of Antipsychotic Medication Adherence in Schizophrenia Through Speech (OBSERVSPEECH)

Schizophrenia is a serious psychiatric illness affecting approximately 25 million people worldwide. Patients with schizophrenia experience hallucinations, auditory illusions, disordered thinking, movement disorders, cognitive impairment and social isolation. Treatments with antipsychotics have proven effective in improving their living conditions, but poor compliance results in relapses and rehospitalizations for the majority of patients, which often results in a worsening of residual symptoms. The prevention of these relapses is a major issue in the care of these patients and frequent monitoring is necessary. The use of a simple, rapid and inexpensive tool to monitor symptoms and treatment effect in schizophrenia could improve the effectiveness of the treatment of these patients and prevent relapses. Speech is a good candidate as a biomarker in the monitoring of patients with schizophrenia. Schizophrenia is accompanied by speech disorders including poor speech, variations in tone or intensity or even difficulties in organizing speech.

Read the detailed description

Schizophrenia is a highly complex disease of unknown origin. It is characterized by a heterogeneous etiology and variable clinical manifestations. Numerous studies have investigated genetic, biochemical or neurodevelopmental factors of the pathology, without providing a definitive answer. The environmental factor is also analyzed, especially urban density and pollution. Finally, the immune pathway, in particular neuroinflammation, has been studied. Certain parasites, such as Toxoplasma, may be involved in the development of schizophrenia in combination with genetic factors. All these studies tend to show that the parasite/gene/environment association would influence the development of schizophrenia, but the origins remain unclear and a more complete knowledge of the pathophysiology is needed to improve diagnosis and patient management through new therapeutic targets.

More than 80% of patients with schizophrenia have language abnormalities. These abnormalities are manifested in syntax, semantics and phonology. The most common include monotonous intonation, poverty of speech, increased pauses, lack of spontaneity, and disruption of speech coherence. As speech is an important factor in social interaction, patients have great difficulty in maintaining their social relationships.

A major problem in schizophrenia is the discontinuation or misuse of antipsychotic treatment, which leads to relapse and additional hospital costs. According to a 2013 study, 50% of patients discontinue treatment after six months, often leading to decompensations.To avoid relapses, clinicans can either administer hetero-questionnaire to monitor the patients' symptoms or monitor treatment adherence.

To monitor symptoms, clinicians have at their disposal various standardized questionnaires such as the PAANS. However, those tests are time-intensive.

To monitor treatment adherence, clinicians can use blood drug concentrations as an evidence of compliance, although this method is invasive, and requires costly administration coordination between healthcare profesionnals and patients. There are also several standardized tests to monitor adherence, such as the clinician-administered BARS questionnaire and the self-administered BEMIB. These measures have often been criticized due to factors such as recall bias and poor self-perception, which limit the accuracy of patient reports and overestimate adherence.

It is therefore essential to develop new tools to objectively measure evolution of symptoms and treatment effects to detect onset of relapses, without increasing the burden on patients' daily lives.

Speech voice markers stand out because they have characteristics that make it easy to use in clinical practice and can be easily integrated into patients' daily lives. Advances in signal processing and machine learning algorithms now make it possible to measure the different components of speech: phonatory skills, articulation, the different linguistic levels (semantics, syntax, morphology, pragmatics) as well as the specific disfluencies of spontaneous speech.

These different speech markers have been validated in different neurological and psychiatric pathologies: in particular, Parkinson's disease, Huntington's disease, depression, suicidal risk, and schizophrenia. These markers of speech in psychiatry are now generalizing across languages and are also being taken into patients' homes to measure changes in patient states.

Distinctive voice characteristics have been a feature of schizophrenia since it was first defined. They are often associated with negative symptoms, such as the inability to show emotion, and with observed social impairments. It has been quantitatively observed that people with schizophrenia have poorer speech, more pauses, distinctive tones, and differences in voice intensity.

Studies have shown antipsychotics also affect language, since patients are dopamine-deficient, and blockade of these receptors by antipsychotics would exacerbate language impairments. In addition, blockade of the striatal dopamine receptor leads to extrapyramidal side effects, causing tremors, muscle rigidity, and tics that interfere with the joint movements required for speech.

Therefore, voice and language are very good candidates as biomarkers in monitoring both symptoms and treatment effects in schizophrenia to detect onsets of relapses.

The aim of this study is to determine whether voice biomarkers can be used to objectively monitor symptoms and treatment effects in schizophrenia in order to detect onset of relapses.

Conditions
Schizophrenia
Being tested
Blood test: measurement of plasma antipsychotic concentration, Voice interviews and questionnaires carried out via the CALLYOPE application
Medical subject headings
Schizophrenia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Blood test: measurement of plasma antipsychotic concentrationBiological

    Four blood tests are prospectively realized per patient during the study to measure the plasma concentration of antipsychotics (primary treatment: risperidone/paliperidone, olanzapine or aripiprazole). These blood samples are taken at the inclusion visit, at the follow-up visits 2 and 4 months after the inclusion visit, then at the end-of-study visit 6 months after the inclusion visit.

  • Voice interviews and questionnaires carried out via the CALLYOPE applicationOther

    Voice interviews carried out via the Callyope application: they consist of a series of tests, divided into two parts: Structured tasks (same content for each participant) and Semi-structured tasks (content varies for each participant).

    The simultaneous analysis of several speech tasks allows us to break down the different stages of speech production and the important factors that influence its achievement.

    In addition, patients will complete self-questionnaires via the application. Finally, lifestyle habits (sleep duration and number of steps) will be recorded via the application.

    These different tests will be carried out on the application at the inclusion visit (M0), then every month (M1, M2, M3, M4, M5) until the end of study visit (M6).

Study groups in NCT06613334
Study groupRoleWhat they receive
Schizophrenic patients treated with a primary treatmentExperimentalStudy's interventions: * 4 blood tests (inclusion visit, at follow-up visits at 2 and 4 months after inclusion, at the end-of-study visit at 6 months after inclusion) to measure the blood concentration of antipsychotic treatment (risperidone or paliperidone) * completion of self-questionnaires and voice interviews of the application developed by CALLYOPE
Receives: Biological: Blood test: measurement of plasma antipsychotic concentration; Other: Voice interviews and questionnaires carried out via the CALLYOPE application

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Voice interviews recorded on Callyope application

    The analysis of the interviews (acoustic and linguistic features) will be implemented in a voice model predicting a score.

    Measured: Month 0, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6

  2. Plasma concentration of antipsychotics

    Plasma concentration of antipsychotics measured in ng/mL from Month 0 to Month 6.

    Measured: Month 0, Month 2, Month 4, Month 6

Secondary outcomes (14)
  1. Age

    Age in years

    Measured: Month 0

  2. Weight

    Weight in kilograms

    Measured: Month 0

  3. Sex

    Sex (Male / Female)

    Measured: Month 0

  4. Change from Baseline in the schizophrenia severity

    Schizophrenia severity will be assessed by the investigator with PANSS (Positive and Negative Syndrome Scale) scale. For positive symptoms, score range is 7-49; For negative symptoms, the score range is 16 to 112. Higher score mean a worse outcome.

    Measured: Month 0, Month 2, Month 4, Month 6

  5. Change from Baseline in the schizophrenia severity

    Schizophrenia severity will be assessed by the investigator with CGI-SH (Clinical Global Impression - Schizophrenia) scale.

    Score range (min - max): 0 - 7 for the severity subscale Symptomatic remission correspond to a score ≤3 (CGI-S).

    Measured: Month 0, Month 2, Month 4, Month 6

  6. Changes from Baseline in the schizophrenia severity

    Schizophrenia severity will be assessed by the investigator with the scores from MCSI (Modified version of the Colorado Symptom Index) questionnaire.

    Score range (min-max) : 5-70 Higher score relates to worse outcome

    Measured: Month 0, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6

  7. Number of hospitalizations

    The total number of schizophrenia-related hospitalizations will be collected by the investigator from enrollment to the end of study at 6 months.

    Measured: From enrollment to the end of study at 6 months

  8. Total sleep duration

    The total sleep duration in hours and minutes will be automatically measured by the Callyope application

    Measured: From enrollment to the end of study at 6 months

  9. Duration of daily physical activity

    Duration of time spent at home, time in stationary mode in hours and minutes automatically assessed by the Callyope application

    Measured: From enrollment to the end of study at 6 months

  10. Phases of sleep duration

    Duration of sleep phases in hours and minutes automatically assessed by the Callyope application

    Measured: From enrollment to the end of study at 6 months

  11. Plasma concentration of sedative antipsychotics

    Plasma concentration of sedative antipsychotics measured in ng/mL from Month 0 to Month 6

    Measured: Month 0, Month 2, Month 4, Month 6

  12. Daily travel distance

    Maximum daily travel distance from home in kilometers automatically assessed by the Callyope application

    Measured: From enrollment to the end of study at 6 months

  13. Changes from Baseline in the symptoms (Depression, anxiety, functional autonomy, fatigue)

    Symptoms will be assessed by the score of the PHQ-9 (Patient Health Questionnaire - 9) questionnaire.

    Score range (min - max): 0 - 27 Higher score relates to a worse outcome

    Measured: Month 0, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6

  14. Changes from Baseline in feelings of loneliness or social isolation

    Feelings of loneliness or social isolation will be assessed by the investigator from the Score from UCLA 3-item Loneliness Scale.

    The total score ranges from 20 to 80. Higher scores indicate higher loneliness.

    Measured: Month 0, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Sep 2024
  2. Study start4 Oct 2024
  3. Primary completionApr 2027 (estimated)
  4. Study completionOct 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Model description
Patients with schizophrenia are assigned prospectively to the following experimental interventions: blood tests to measure antipsychotics concentration and the administration of questionnaires/voice tests on the CALLYOPE application.
Masking
None (open label)
Enrolment
200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06613334
Sponsor's protocol ID
D23-P038
Acronym
OBSERVSPEECH
Status last verified
Sep 2026
First submitted
10 Sep 2024
Last updated
21 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Blood test: measurement of plasma antipsychotic concentration and Voice interviews and questionnaires carried out via the CALLYOPE application in people with Schizophrenia, run by Centre Hospitalier St Anne at 2 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 10 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 21 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Pierre De Maricourt, Dr ((0)1 45 65 86 91 ext. +(33), P.DEMARICOURT@ghu-paris.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Voice interviews recorded on Callyope application (time frame: Month 0, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Sep 2026; AzTrials last refreshed its copy on 8 Nov 2026.

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