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Comparing Telepractice and Conventional Face-to-face Voice Therapy

Voice Therapy for Benign Voice Disorders in the Elderly: A Randomized Controlled Trial Comparing Telepractice and Conventional Face-to-face Therapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02922309
Enrollment
69
Registered
2016-10-04
Start date
2016-10-17
Completion date
2018-12-19
Last updated
2020-02-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aged, Dysphonia, Speech Therapy

Brief summary

People over 55 years are high-risk with voice disorders. Voice disordered elderly need vocal training in order to improve communication efficiency and quality of life. However, participation in vocal training of elderly is often restricted by motivation, time of practice, and availability to hospital, which thus reduces treatment effects. The purpose of the study is to design a telecommunication vocal training system and a vocal training program for voice disordered elderly in Taiwan. The investigator proposed a 3-year consecutive study, including a single-blind, randomized controlled trial, to test the hypothesis that vocal training via telepractice for voice disordered elderly are not inferior to the standard face to face training.

Detailed description

Randomization: per mutated block, 40 patients on each arms (experimental and control) Allocation: sealed envelope indicating either of the 2 groups Intervention: weekly vocal training, each course last for 30-40 minutes,lasting for 2 months Outcome measurement: before treatment, 1 month, 3 months, and 6 months after treatment Primary outcome: 10-item voice handicap index Secondary outcome: acoustics and aerodynamic parameter

Interventions

BEHAVIORALVocal Training Via Telepractice

Vocal Training Via Telepractice, delivered by integrated communication service

BEHAVIORALVocal Training Via face-to face practice

Vocal Training Via face-to face practice at medical facilities

Sponsors

Far Eastern Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patient equal or older than 55 years old * Voice Handicap Index-10 (VHI-10) score \>10 point * accessibility to a network connection

Exclusion criteria

* neurologic disorders * active pulomanory disease * mental disorder

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline of 10-item voice handicap index at 2 monthsbefore treatment (after signing informed consent, prior to randomization) and within 2 weeks after the completion of voice therapymin: 0(best); Max: 40(worst);

Other

MeasureTime frameDescription
Jitterbefore treatment (after signing informed consent, prior to randomization) and within 2 weeks after the completion of voice therapypercentage of jitter based on continuous vowel
Shimmerbefore treatment (after signing informed consent, prior to randomization) and within 2 weeks after the completion of voice therapydecibel (dB) of shimmer based on continuous vowel
Noise to harmonic ratiobefore treatment (after signing informed consent, prior to randomization) and within 2 weeks after the completion of voice therapyNoise to harmonic ratio based on continuous vowel
Perceptual Analysis using grade, roughness, breathiness, asthenia, and strainbefore treatment (after signing informed consent, prior to randomization) and within 2 weeks after the completion of voice therapyfrom 0(best) to 3(worst)
Maximal phonation timebefore treatment (after signing informed consent, prior to randomization) and within 2 weeks after the completion of voice therapyseconds
VLSbefore treatment (after signing informed consent, prior to randomization) and within 2 weeks after the completion of voice therapyVideolaryngostroboscopy (mucosal wave: normal, mildly decreased, severely decreased, absent)
smoothed Cepstrum peak prominencebefore treatment (after signing informed consent, prior to randomization) and within 2 weeks after the completion of voice therapybased on reading a Mandarin passage

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026