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Trial · NCT07904858

Registered outcomes16

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryForced Vital Capacity (FVC)Baseline (immediately before) and immediately after the single intervention session (same day)FVC in liters (L), measured with a CHEST HI-801 spirometer.
PrimaryResting Minute VentilationBaseline (immediately before) and immediately after the single intervention session (same day)Minute ventilation during quiet breathing in liters per minute (L/min), measured with a CHEST HI-801 spirometer.
PrimaryForced Expiratory Volume in 1 Second (FEV1)Baseline (immediately before) and immediately after the single intervention session (same day)FEV1 in liters (L), measured with a CHEST HI-801 spirometer.
PrimaryPeak Expiratory Flow (PEF)Baseline (immediately before) and immediately after the single intervention session (same day)PEF in liters per second (L/s), measured with a CHEST HI-801 spirometer.
PrimaryMaximal Voluntary Ventilation (MVV)Baseline (immediately before) and immediately after the single intervention session (same day)MVV in liters per minute (L/min), measured with a CHEST HI-801 spirometer.
PrimaryResting Tidal VolumeBaseline (immediately before) and immediately after the single intervention session (same day)Tidal volume during quiet breathing in liters (L), measured with a CHEST HI-801 spirometer.
PrimaryResting Respiratory RateBaseline (immediately before) and immediately after the single intervention session (same day)Respiratory rate during quiet breathing in breaths per minute, measured with a CHEST HI-801 spirometer.
PrimaryVentilatory ReserveBaseline (immediately before) and immediately after the single intervention session (same day)Ventilatory reserve in percent (%), calculated by the CHEST HI-801 spirometer from resting minute ventilation relative to MVV.
SecondaryStandard Deviation of Fundamental Frequency During Sustained NoteBaseline (immediately before) and immediately after the single intervention session (same day)Standard deviation of the fundamental frequency in hertz (Hz) during a sustained G4 note, extracted with automated pYIN-based acoustic analysis.
SecondaryMean Fundamental Frequency During Sustained NoteBaseline (immediately before) and immediately after the single intervention session (same day)Mean fundamental frequency in hertz (Hz) during a sustained G4 note, extracted with automated pYIN-based acoustic analysis.
SecondaryLowest Attainable PitchBaseline (immediately before) and immediately after the single intervention session (same day)Lowest fundamental frequency in hertz (Hz) reached during a descending pitch-range task.
SecondaryMaximal loudnessBaseline (immediately before) and immediately after the single intervention session (same day)Peak sound level in decibels relative to full scale (dBFS) during a G major arpeggio played at maximal controllable loudness.
SecondaryHighest Attainable Pitch (Hz)Baseline (immediately before) and immediately after the single intervention session (same day)Highest fundamental frequency in hertz (Hz) reached during an ascending pitch-range task.
SecondaryHighest Attainable Pitch (MIDI Semitones)Baseline (immediately before) and immediately after the single intervention session (same day)Highest pitch reached during the ascending pitch-range task, converted to MIDI semitone units.
SecondaryRating of perceived exertionBaseline (immediately before) and immediately after the single intervention session (same day)
Rating of perceived exertion on the Borg 6-20 scale (minimum 6, maximum 20; higher scores indicate greater perceived exertion, i.e., a worse outcome), rated immediately after a high-register melody task.
SecondarySustained-note durationBaseline (immediately before) and immediately after the single intervention session (same day)Duration in seconds (s) of a sustained G4 note played as long as possible.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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