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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05492266
Other study ID # STUDY21120032
Secondary ID 5R21DC017553-03
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 2024
Est. completion date September 2025

Study information

Verified date February 2024
Source University of Pittsburgh
Contact Amber D Shaffer, PhD
Phone 412-692-6874
Email shafferad@upmc.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

When the soft palate does not move enough because of a cleft palate or for unknown reasons, this can lead to a speech difference called velopharyngeal insufficiency. The purpose of this research study is to test if soft palate exercises using a hand help breathing device will help improve the ability of the soft palate to close the area between the throat and nose and help improve speech.


Description:

The objective of this study is to examine the feasibility and efficacy of expiratory muscle strength training to improve velopharyngeal closure in patients with velopharyngeal dysfunction and nasal air emissions. A randomized, controlled trial will be conducted at a cleft craniofacial center at a tertiary children's hospital. Patients will be block randomized based on Pittsburgh Weighted Speech Scale (PWSS) score (3-6 or 7+) to Expiratory Muscle Strength Training for 6 to 8 weeks or no exercises. Patients with reductions in PWSS during this time will be further randomized to EMST maintenance training for 6 months or no exercises.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date September 2025
Est. primary completion date February 2025
Accepts healthy volunteers No
Gender All
Age group 5 Years to 17 Years
Eligibility Inclusion Criteria: - Pittsburgh weighted speech scores of 3 or greater - Ages 5-17 years Exclusion Criteria: - Previous speech surgery (e.g. palatoplasty or pharyngeal flap) - Speech surgery scheduled within the next 56 days - Unable or unwilling to perform the tests and exercises outlined in the study

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Expiratory Muscle Strength Training
At visit 1, participants will be block randomized based on PWSS score (3-6 or 7+) to Expiratory Muscle Strength Training (EMST) for 6 to 8 weeks or no exercises. Participants in the EMST-150 group will perform 5 sets of 5 resistive expirations once a day with a 10-15 second rest between each repetition and a 1-2 minute rest between each set of 5 repetitions.
Maintenance Training
At visit 2, participants with improved (decreased) PWSS of 2 or more points, for whom the family and/or surgeon is not currently considering surgical intervention for VPI, will be further randomized to continue "maintenance" EMST exercises or no exercises for 6 months. Participants in the "maintenance" group will complete 3-5 sessions exercise sessions each week (rather than daily training), with 2 sets of 5 resistive expirations (rather than 5 sets)

Locations

Country Name City State
United States UPMC Children's Hospital of Pittsburgh Pittsburgh Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Noel Jabbour National Institute on Deafness and Other Communication Disorders (NIDCD)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Change in nasalance scores after 6 months of maintenance exercises compared with after the initial 6-8 weeks of exercises Percent change in nasalance measured during nasometry 6-8 weeks and 8 months
Other Change in perceptual speech symptoms of velopharyngeal dysfunction after 6 months of maintenance exercises compared with after the initial 6-8 weeks of exercises Perceptual symptoms of velopharyngeal incompetence measured using the Pittsburgh Weighted Speech Score, on a scale of 0-23, with =7 indicating likely velopharyngeal incompetence 6-8 weeks and 8 months
Other Change in oral pressure after 6 months of maintenance exercises compared with after the initial 6-8 weeks of exercises Percent change in pressure achieved when blowing through the EMST-150 6-8 weeks and 8 months
Other Change in velopharyngeal flutter after 6 months of maintenance exercises compared with after the initial 6-8 weeks of exercises Change in percentage of participants with oscillating oral pressure when blowing through the EMST-150 6-8 weeks and 8 months
Other Change in oral pressure decay after 6 months of maintenance exercises compared with after the initial 6-8 weeks of exercises Ratio of the magnitude of oral pressure decay when blowing through the EMST-150 6-8 weeks and 8 months
Other Prevalence of surgical intervention Percentage of patients undergoing surgical intervention for speech symptoms within the 1 year following enrollment 1 year
Primary Change in nasalance scores after 6-8 weeks of exercises compared with baseline Percent change in nasalance measured during nasometry Baseline and 6-8 weeks
Primary Change in perceptual speech symptoms of velopharyngeal dysfunction following 6-8 weeks of exercises compared with baseline Perceptual symptoms of velopharyngeal incompetence measured using the Pittsburgh Weighted Speech Score, on a scale of 0-23, with =7 indicating likely velopharyngeal incompetence Baseline and 6-8 weeks
Primary Change in oral pressure following 6-8 weeks of exercises compared with baseline Percent change in oral pressure achieved when blowing through the EMST-150 Baseline and 6-8 weeks
Primary Change in velopharyngeal flutter following 6-8 weeks of exercises compared with baseline Change in percentage of participants with oscillating oral pressure when blowing through the EMST-150 Baseline and 6-8 weeks
Primary Change in oral pressure decay following 6-8 weeks of exercises compared with baseline Ratio of the magnitude of oral pressure decay when blowing through the EMST-150 Baseline and 6-8 weeks
Secondary Change in VELO questionnaire scores following 6-8 weeks of exercises compared with baseline Percent change in Velopharyngeal Insufficiency (VPI) Effects on Life Outcomes (VELO) scores. Scores range from 0 - 100, with 100 representing the highest QOL Baseline and 6-8 weeks
Secondary Resolution of type B tympanogram following 6-8 weeks of exercises compared with baseline. Percentage of participants with a change in tympanogram type from type B (flat) to type A (normal middle ear function). Baseline and 6-8 weeks
Secondary Resolution of type C tympanogram following 6-8 weeks of exercises compared with baseline. Percentage of participants with a change in tympanogram type from type C (negative pressure) to type A (normal middle ear function). Baseline and 6-8 weeks
Secondary Resolution of effusion following 6-8 weeks of exercises compared with baseline. Percentage of participants with resolution of middle ear effusion based on otoscopy. Baseline and 6-8 weeks
Secondary Resolution of retraction following 6-8 weeks of exercises compared with baseline. Percentage of participants with resolution of tympanic membrane retraction based on otoscopy Baseline and 6-8 weeks
See also
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