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NCT Number: NCT06874322

Voiceitt for People With Impairments in Speech

The primary objective of this pilot study is to evaluate the feasibility and preliminary effectiveness of the Voiceitt app in improving communication for individuals with speech impairments due to conditions such as cerebral palsy (CP), stroke, Amyotrophic Lateral Sclerosis (ALS), or Parkinson's disease.

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Key information

Age range

13 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Center for Assistive Technology

Pittsburgh, Pennsylvania, 15213, United States

Location status: Recruiting

Location contact

Brad E Dicianno, MD

CONTACT

[email protected]

(412) 648-6666

Brad E Dicianno, MD

PRINCIPAL_INVESTIGATOR

Katya Hill, PhD, CCC-SLP

CONTACT

[email protected]

412-383-6659

Katya Hill, PhD,CCC-SLP

SUB_INVESTIGATOR

About this study

Conditions like CP, ALS, Stroke or Parkinson's disease, etc., cause communication impairment. There are few augmentative communication options that allow people with these impairments to communicate effectively.

Voiceitt is an app that is designed to assist people with speech impairments by using a voice recognition and dictation tool that adapts to users' unique, non-standard speech patterns. However, its effectiveness in clinical populations has not been established. This study is bridging the gap in evaluating the preliminary effectiveness and feasibility of Voiceitt app in improving communication among people with mild to moderate speech impairments.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 13 or older
  • moderately severe speech dysarthria due to conditions such as CP, stroke, ALS or Parkinson's Disease, etc.
  • Ability to understand and follow instructions for using the Voiceitt app.

Exclusion criteria

  • Severe cognitive impairments that prevent the understanding of the Voiceitt app and required training.
  • Patients who have additional speech impairments other than dysarthria, such as significant aphasia or verbal apraxia.
  • Severe physical impairments that prevent interaction with the app.
  • Non-English speakers.

Treatment and study plan

Voiceitt

Other

Participants will use Voiceitt App

Primary outcomes

  1. Change in Communication Abilities as measured by SIR

    Time frame: Baseline (Day 1), 5-6 months, and 7-8 months

    Change in Communication Abilities as measured by Speech Intelligibility Rating (SIR) that quantifies clarity of speech. The rating ranges from 1-5. low rating means speech is unintelligible, and highest rating means speech is intelligible to all listeners. Change in SIR is measured by administering SIR at 3 different time points, at baseline, and two times after intervention.

  2. Change in Communication Abilities as measured by Communication Effectiveness Index (CETI)

    Time frame: Baseline (day 1), 5-6 months, and 7-8 months

    Change in Communication Abilities as measured by Communication Effectiveness Index (CETI) that measures perceived effectiveness of communication in daily activities. CETI is a 16 item questionnaire. Each item is scored from 1-100. The final score of CETI is the averaged score across the 16 items, and ranges from 1-100. A high score indicates good performance in functional communication and a low score, poor performance. Change in CETI is measured by administering CETI at 3 different time points, at baseline, and two times after intervention.

Secondary outcomes

  1. User Satisfaction

    Time frame: 7-8 months

    User satisfaction is assessed through surveys and interviews focusing on ease of use, satisfaction with the app, and perceived changes. The survey uses Likert-type scale where users choose the answer option that represent their assessment of the app on several usability questions. An example of the question-and-answer choices is "How easy was it to set up the Voiceitt app? Very easy, Easy, Neutral, Difficult, Very difficult." Reported data will be a combination of frequency of participants choosing favorable and unfavorable answer choices, and a qualitative analysis based on participants' responses to the survey and interview.

  2. Change in Communication-Related Frustration

    Time frame: 7-8 months

    Self-reported change in frustration levels during communication.

  3. Change in Participants' Accounts on Social Interaction Quality

    Time frame: 7-8 months

    Through qualitative interviews, participants will be asked about how the app influenced their social interactions and participation in daily activities. This information will be reported qualitatively as themes using qualitative analysis.

Study contacts

Contact information is provided by the study sponsor or research team.

Brad E Dicianno, MD

CONTACT

[email protected]

(412) 648-6666

Zara Ambadar, Ph.D

CONTACT

[email protected]

4126086118

Sponsors and collaborators

Lead sponsor

University of Pittsburgh

Other

Collaborators

  • Duquesne University

Registry information

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Mar 13, 2025
Registry last updated
Jul 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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