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Testing a Smart Phone App to Enhance Voice Therapy Adherence

Testing a Smart Phone App to Enhance Voice Therapy Adherence

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04002336
Enrollment
33
Registered
2019-06-28
Start date
2018-10-01
Completion date
2018-11-30
Last updated
2019-06-28

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

Conditions

Voice Disorders

Keywords

adherence

Brief summary

The current project is designed as phase 1 study conducted to improve/enhance normal voice. Fifteen Thirty non-treatment seeking individuals, with no identifiable vocal pathology on laryngeal examination, will be randomized to one of two groups; 1) Voice therapy delivery without App (control/standard of care), 2) Voice therapy delivery with app (experimental). Participants in both groups will attend weekly voice therapy sessions (for 6 weeks) with the PI and Co- I (Joseph Stemple). Control group participants will be provided with an audio file of the exercises, and an exercise log sheet to track progress. Experimental group participants will use the smartphone app, which allows participants to record home practice sessions in real time and upload sessions to the app server for the clinician to access and track. Three-wave surveys will be conducted at the baseline, four weeks and 6 weeks after the intervention. Other data sources include study administration, exercise logs, app data, and clinical assessment.

Interventions

BEHAVIORALTraditional Voice therapy

Traditional method of voice therapy

BEHAVIORALVoice Therapy App

Smartphone app, which allows participants to record home practice sessions in real time and upload sessions to the app server for the clinician to access and track.

Sponsors

Vrushali Angadi
Lead SponsorOTHER

Study design

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

Masking description

Single-blinded to primary outcome measure

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Adults \> 18 years 2. Non-smokers 3. Hearing level within normal limits 4. Absence of vocal fold pathology as confirmed by MD on laryngeal examination 5. Agree to avoid vocally abusive behaviors for the entirety of the study

Exclusion criteria

1. Apple phone (iOS) 2. Impaired hearing 3. Uncontrolled asthma 4. Smoking 5. H/o vocal fold surgery 6. Presence of vocal fold pathology 7. Previous history of experience with VFE performance 8. Non-English speaking participants

Design outcomes

Primary

MeasureTime frameDescription
Adherence6 weeksNumber of completed home practice sessions

Secondary

MeasureTime frameDescription
MPT (maximum phonation time)6 weeksMaximum phonation time

Countries

United States

Outcome results

None listed

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