Skip to main content
OpenTrials
Enrolling by Invitation

NCT Number: NCT07176013

Immersive Virtual Reality Meditation in Voice Therapy

This study aims to explore the feasibility of incorporating regular guided meditations via immersive virtual reality (IVR) at the start of voice therapy sessions to facilitate better learning and retention of treatment. The study will involve 30 participants, and use the TRIPP application with the Meta Quest 2 virtual reality headset, known for its immersive meditation experiences designed to calm or focus the user. The objective is to investigate the immediate effects of meditation/mindfulness in IVR on vocal production, with the goal of improving self-regulation, attentional focus, and reducing vocal hyperfunction. IVR has been utilized in mental health settings and exposure therapy for various conditions, but its application in voice therapy, particularly for anxiety reduction through fully immersive meditation, remains unexplored. The study seeks to determine whether IVR can enhance therapy outcomes by improving engagement, attention, and vocal control in individuals undergoing voice therapy, potentially maximizing treatment gains. Through this research, the aim is to assess the efficacy of IVR in enhancing voice therapy interventions and addressing the unique challenges posed by stress and anxiety in voice users.

Enrolling by Invitation

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mount Sinai Downtown Union Square

New York, 10003, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with voice disorders, difficulties or laryngeal hypersensitivity, and who also have anxiety
  • Must have availability to participate for entire course of 5 consistent weeks

Exclusion criteria

  • Anyone not meeting inclusion criteria
  • Presence of any additional medical condition significantly affecting:
  • Respiratory function (e.g., advanced lung disease)
  • Laryngeal function (e.g., status-post deep brain stimulation)
  • Lingual function
  • Velopharyngeal function (e.g., laryngectomy)

Treatment and study plan

Voice therapy

Behavioral

All patients will receive a course of voice therapy as normal.

Meditation

Behavioral

Meditation at the start of each session. (each session is 30 minutes)

Virtual reality

Device

TRIPP application in the Meta Quest 2 Virtual Reality Headset.

Primary outcomes

  1. Maximum Phonation Time (MPT)

    Time frame: at each therapy session (approximately 1 week apart over 4 weeks)

    MPT will be used to assess participants' maximum phonation time. The speech evaluator instructs the patient to take a comfortable breath and then produce the sound /a/ for as long as possible. The task is performed twice, and the maximum duration of the two measurements is used.

  2. Noise-to-Harmonic Ratio (NHR)

    Time frame: Pre-intervention (within 1 week before first session) and post-intervention (within 1 week after final session

    NHR is a parameter in MDVP that represents ratio of non-harmonic and harmonic waves in a certain sound wave period. NHR describes the quality of the amount of noise in the sound. Inadequate closure of the vocal cords and periodic vibrations of the vocal cords cause excessive air flow as it passes through the vocal cords, causing turbulence and noise. Normal and periodic sound signals will have a small NHR, while dysphonia sound signals will have a large NHR value.

  3. Cepstral Peak Prominence (CPPS)

    Time frame: Pre-intervention (within 1 week before first session) and post-intervention (within 1 week after final session

    Cepstral Peak Prominence (CPPS) is an indicator of voice quality. It is measured in decibels. An increase in CPPS value indicates an improvement in voice symptoms.

  4. Acoustic Vocal Quality Index (AVQI)

    Time frame: Pre-intervention (within 1 week before first session) and post-intervention (within 1 week after final session

    The acoustic voice quality index (AVQI) is a multiparametric score to quantify vocal quality. It is based on a weighted combination of 6 voice parameters: smoothed cepstral peak prominence (CPPS), harmonics-to-noise ratio (HNR), shimmer local (SL), shimmer local dB (SLdB), general slope of the spectrum (slope) and tilt of the regression line through the spectrum (tilt). The formula is constructed as 9.072 - 0.245 × CPPs - 0.161 × HNR - 0.470 × SL + 6.158 × SLdB - 0.071 × Slope - 0.170 × Tilt and ranges from 0 to 10. A lower score correlates with a better vocal quality.

Secondary outcomes

  1. Voice Handicap Index

    Time frame: Pre-intervention (within 1 week before first session) and post-intervention (within 1 week after final session

    The Voice Handicap Index (VHI) is a validated 10-item questionnaire measuring the impact of voice challenges on quality of life (QOL). Scores range from 0 to 40, with higher scores indicating greater perceived voice handicap and negative impact on daily functioning.

  2. State Trait Anxiety Inventory Y-1 (STAI-1), long form

    Time frame: Pre-intervention (within 1 week before first session) and post-intervention (within 1 week after final session

    The State Anxiety Inventory (STAI Y-1) long form assess the severity of current state of anxiety in the moment, with a minimum score of 40 and max of 80, where scores >37 indicates moderate-severe state anxiety. Higher score indicates more severity of anxiety

  3. State Trait Anxiety Inventory Y-1 (STAY Y-1), short form

    Time frame: Immediately pre- and immediately post-meditation in each therapy session, over approximately 4 weeks

    The State Anxiety Inventory-Short Form (STAI Y-1) assesses severity of current state of anxiety in the moment to determine immediate effects of meditation. Scores range from 20-40. Higher score indicates more severity of anxiety.

  4. State Trait Anxiety Inventory Y-2 (STAI Y-2), long form

    Time frame: Pre-intervention (within 1 week before first session) and post-intervention (within 1 week after final session

    The State Trait Anxiety Inventory (STAI Y-2) assesses severity of anxiety relative to how the patient "generally" feels. Scores range 40-80, with scores >37 indicating moderate-severe trait anxiety. Higher score indicates more severity of anxiety.

  5. Vocal Fatigue Index

    Time frame: Pre-intervention (within 1 week before first session) and post-intervention (within 1 week after final session

    The Vocal Fatigue Index (VFI) is a validated questionnaire designed to measure three distinct dimensions of vocal fatigue and voice disorders. It evaluates scores across three subscales:

    Fatigue and Avoidance (Part 1): Scores range from 0 to 44, with scores ≥24 indicating severity.

    Physical Discomfort (Part 2): Scores range from 0 to 20, with scores ≥7 indicating severity.

    Improvement with Rest (Part 3): Scores range from 0 to 12, with scores ≤7 indicating severity.

    Higher scores on Parts 1 and 2, and lower scores on Part 3, indicate greater voice disorder severity. The VFI is intended to be used for the score of each subscale individually and is not validated to measure severity based on the composite score. However, the maximum total score across all three subscales is 79.

  6. CAPE-V, Consensus on Auditory-Perceptual Evaluation of Voice

    Time frame: Pre-intervention (within 1 week before first session) and post-intervention (within 1 week after final session

    A subjective auditory-perceptual evaluation to judge the severity of dysphonia from the standpoint of expert clinician raters (at least 2 for each sample, not including the treating clinician). Scale of severity overall from 0-100. Higher score indicates more severity of symptoms.

  7. Heart rate measured in beats per minute

    Time frame: Immediately pre- and immediately post-meditation in each therapy session, over approximately 4 weeks

    Heart rate (HR) is measured in beats per minute (bpm) using a standard hospital-provided pulse oximeter to assess cardiovascular function.

Sponsors and collaborators

Lead sponsor

Icahn School of Medicine at Mount Sinai

Other

Registry information

Official study title

Immediate and Cumulative Effects of Meditation on Voice Therapy Using Immersive Virtual Reality (IVR)

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Sep 16, 2025
Registry last updated
Feb 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.