Effects of Finger Kazoo Exercise With and Without Oropharyngeal Enlargement in the Operatic Singing Voice (FIKVOX)

Aveiro University

Status: Completed

Conditions: Voice Alteration

Treatments: Behavioral: Condition A; Behavioral: Condition B

Study type: Interventional

Funder types: Other

Identifiers

NCT07129668

doi.org/10.54499/2023.0361.BD (Other Grant/Funding Number)

10-CE/2025

Details and patient eligibility

About

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.

Enrollment: 15 patients

Sex: All

Ages: 18 to 55 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 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.

Exclusion criteria

• 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.

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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15 participants in 3 patient groups

Condition A

Active Comparator group

Description:

Without Oropharyngeal Enlargement

Treatment:

Behavioral: Condition B

Behavioral: Condition A

Condition B

Active Comparator group

Description:

With Oropharyngeal Enlargement

Treatment:

Behavioral: Condition B

Behavioral: Condition A

Condition 0 or Baseline

Active Comparator group

Description:

Condition 0 (Baseline) consists of producing the target vocal tasks without any semi-occlusion or intentional oropharyngeal modification just a pre vocal warmup.

Treatment:

Behavioral: Condition B

Behavioral: Condition A