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Voice Technology to Identify Opioid Use

16. mai 2026 oppdatert av: Tenvos Inc.

Using Voice Technology to Identify Opioid Use in Patients in Treatment for Opioid Use Disorder

This study explored whether changes in a person's voice could help identify opioid use in patients with opioid use disorder (OUD). Current methods for determining whether a patient is intoxicated or in withdrawal often rely on self-reporting and clinical judgment, which can be subjective and inconsistent. Drug tests are logistically challenging to administer and can be costly with repeated use.

The project investigated whether physiological changes associated with opioid use could be detected through speech analysis technology. Researchers evaluated whether machine learning methods could identify voice patterns associated with opioid intoxication or withdrawal.

The primary goal of the study was to assess the accuracy of voice-based biomarkers in identifying opioid use. The study also explored relationships between opioid use and specific speech characteristics.

Studieoversikt

Status

Fullført

Forhold

Detaljert beskrivelse

This study investigated whether changes in a person's voice could be used to identify opioid use in individuals with opioid use disorder (OUD). The opioid epidemic continues to present significant public health, medical, and social challenges in the United States and globally. Clinicians treating patients with OUD often need to determine whether a patient may be actively using opioids, intoxicated, withdrawing, or responding appropriately to treatment. Current approaches commonly rely on self-reporting, interviews, behavioral observations, urine toxicology testing, and clinical judgment. While these methods can be useful, they may also be subjective, resource-intensive, intermittent, invasive, or difficult to implement frequently in routine care settings.

The purpose of this project was to evaluate whether speech analysis technology could provide a more objective, scalable, and non-invasive approach for monitoring opioid-related physiological changes. Human speech is a complex neuromuscular activity that depends on the coordinated function of the brain, respiratory system, vocal tract, and facial musculature. Opioids can affect cognitive processing, respiratory patterns, motor coordination, reaction time, sedation levels, and muscle control, all of which may influence characteristics of speech production. Prior scientific literature has suggested that physiological and neurological conditions can sometimes produce measurable changes in speech patterns. This project sought to determine whether similar measurable changes could be associated with opioid use.

The study focused specifically on analyzing speech recordings from participants with opioid use disorder. Researchers collected voice samples and applied computational analysis methods to evaluate whether acoustic and temporal speech features could distinguish opioid-related states. The project used signal-processing techniques and machine learning methods to analyze a range of speech characteristics that may reflect physiological effects associated with opioid exposure.

Evaluated speech features included acoustic biomarkers commonly studied in speech analytics research. The project investigated whether combinations of these features could be used to identify patterns associated with opioid intoxication or withdrawal.

A major goal of the study was to assess the feasibility of using speech as a physiological biomarker for opioid use monitoring. Researchers evaluated whether machine learning models could reliably differentiate between opioid-related conditions using speech data alone.

The primary objective of the study was to assess the accuracy and feasibility of voice-based biomarkers for identifying opioid use in individuals with OUD. The study also aimed to better understand the limitations and challenges associated with speech-based impairment detection.

As part of the research effort, the project contributed to the development of internal workflows and analytic infrastructure for handling sensitive speech data. Researchers established preprocessing pipelines for audio ingestion, normalization, feature extraction, labeling, quality control, and model evaluation.

The work generated technical findings regarding the feasibility of speech-based opioid detection and highlighted several scientific and engineering challenges associated with this problem space. These included variability in recording environments, differences between speakers, background noise, individual physiological differences, and the difficulty of isolating opioid-related speech effects from unrelated sources of variation. The study also reinforced the challenges associated with developing generalized machine learning classifiers for complex real-world physiological states using speech data alone.

Although the project explored the potential for objective opioid monitoring through speech analysis, the research did not produce a clinically deployable classifier during the study period. However, the project generated valuable information regarding the limitations, feasibility considerations, and technical barriers associated with speech-based opioid detection approaches. These findings informed future research planning, technology-development decisions, and evaluation strategies for impairment-detection technologies.

Overall, the project contributed to ongoing research efforts exploring non-invasive digital biomarkers for substance-use monitoring. The findings from this work may help guide future investigations into speech analytics, physiological monitoring, and machine learning approaches for identifying substance-related impairment and supporting clinical decision-making in addiction medicine settings.

Studietype

Observasjonsmessig

Registrering (Faktiske)

41

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • California
      • Loma Linda, California, Forente stater, 92350
        • Loma Linda University Health, 24951 Circle Drive, Nichol Hall, Room #2042

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Prøvetakingsmetode

Sannsynlighetsprøve

Studiepopulasjon

The study population is adult (18+) English-speaking men and women currently receiving OUD treatment at the Volpicelli Center, capable of consenting and completing the protocol, and free of severe psychiatric comorbidity or chronic speech-affecting conditions. Because participants are drawn from an active treatment population, they are by definition individuals already engaged in care for OUD rather than treatment-naïve or general-population samples - a relevant consideration when interpreting how the voice biomarker findings might generalize.

Beskrivelse

Inclusion Criteria:

  • Male or female
  • At least 18 years old
  • Be an active patient in treatment at the Volpicelli Center
  • Have a diagnosis of Opioid Use Disorder (OUD)
  • Ability to read English
  • Able to comprehend and are willing to sign the informed consent form and are able to adhere to the protocol

Exclusion Criteria:

  • Severe psychiatric comorbidity
  • A chronic medical condition that interferes with speaking (note: Acute conditions that impair speech or hearing will not be considered exclusionary, but testing will be deferred until the temporary condition has been resolved)
  • Non-fluency in the study language (English)

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
Patients in treatment for opioid use disorder at the Volpicelli Center.
Prospective longitudinal observational cohort study with repeated measures where each participant completed two visits approximately 30 days apart with repeated speech and clinical measurements. This is a prospective observational study therefore no intervention will be applied.
Not Applicable - Observational Study

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Sensitivity and Specificity
Tidsramme: 12 months after the enrollment
Sensitivity and Specificity of the machine learning model when classifying voice samples into patient's state based on their speech.
12 months after the enrollment

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
List of specific voice features/categories affected by substances
Tidsramme: 12 months after enrollment
Identify voice features/categories most affected by the following substances: Buprenorphine, Other Opioid, Opioid Antagonist, Stimulant, Sedative, Cannabinoid.
12 months after enrollment

Samarbeidspartnere og etterforskere

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Publikasjoner og nyttige lenker

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Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

10. desember 2024

Primær fullføring (Faktiske)

30. juni 2025

Studiet fullført (Faktiske)

30. januar 2026

Datoer for studieregistrering

Først innsendt

10. mai 2026

Først innsendt som oppfylte QC-kriteriene

16. mai 2026

Først lagt ut (Faktiske)

22. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

22. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

16. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 0612
  • 1R43DA060696-01 (U.S. NIH-stipend/kontrakt)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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