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临床试验/NCT07129668
NCT07129668已完成不适用

Effects of Finger Kazoo Exercise With and Without Oropharyngeal Enlargement in the Operatic Singing Voice: A Randomized, Single-Blind, Crossover Controlled Clinical Trial

Aveiro University2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2025年5月30日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
15
试验地点
2
主要终点
Maximum Phonation Time (MPT) variation between conditions without and with oropharyngeal enlargement.

研究概览

简要总结

This clinical trial aimed to evaluate the effects of the semi-occluded vocal tract exercise Finger Kazoo (FK), with and without oropharyngeal expansion, on the singing voice. Fifteen classically trained singers, screened using the Singing Voice Handicap Index-10 (SVHI-10), participated in a randomized, single-blind, crossover trial with two experimental sessions separated by 48 hours. Participants were randomized via Sealed Envelope to start in Condition A (without oropharyngeal expansion) or Condition B (with oropharyngeal expansion). In each session, standardized recordings were obtained before and after the intervention, including maximum phonation time for the vowels /a/ and /i/, and an operatic aria excerpt. Acoustic analysis (PRAAT) extracted fundamental frequency (F0), jitter, and shimmer. Comparisons between baseline and experimental conditions were performed using paired-samples t-tests, Wilcoxon tests, robust paired t-tests, and Friedman ANOVA with Durbin-Conover, Tukey, Bonferroni, and Holm post hoc corrections, with a 95% confidence interval. Auditory-perceptual evaluation was conducted by 15 blinded experts using the EAI Scale Form, with balanced sample distribution among raters. Self-perceptual evaluation was also performed by participants using the same scale.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Classically trained singers aged 18 to 45 years.
  • Scoring below the cutoff for vocal handicap on the Singing Voice Handicap Index-10 (SVHI-10 ≤ 6 )*.
  • No history of recently vocal fold pathology or laryngeal surgery.
  • Non-smokers and no current upper respiratory infection.
  • Willingness and ability to attend two experimental sessions spaced 48 hours apart.

排除标准

  • Presence of any current voice disorder or history of chronic laryngeal disease.
  • Recent respiratory infection within 2 weeks prior to enrollment.
  • Use of medications affecting voice or respiratory function.
  • Inability or unwillingness to comply with study protocol.

结局指标

主要结局

Maximum Phonation Time (MPT) variation between conditions without and with oropharyngeal enlargement.

时间窗: Baseline and 48 hours after first session (allowing return to baseline before second session).

Assessment of the difference in maximum phonation time (in seconds) between two experimental conditions: without oropharyngeal enlargement (Condition A) and with oropharyngeal enlargement (Condition B), during sustained vowel phonation. Data Collection Method: Acoustic recordings obtained using Praat software. The MPT was measured from the onset of phonation to cessation, with participants instructed to sustain the vowel at comfortable pitch and loudness. Analysis Method: Robust Paired Samples T-Test comparing MPT between Condition A and Condition B. Effect sizes calculated using Cohen's d. Results Summary: Mean MPT was significantly higher in Condition B (+7.9 s; p \< .001; d = 0.46), indicating improved phonatory efficiency.

次要结局

  • Change in Fundamental Frequency Stability (ΔF0) between conditions without and with oropharyngeal enlargement.(Baseline and 48 hours after first session (allowing return to baseline before second session).)

研究者

发起方
Aveiro University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jean Carlos Gorges

Principal Investigator

Aveiro University

研究点 (2)

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