Preliminary Studies to Test the Effects of Ambulatory Biofeedback in Small Groups of Patients With Vocal Hyperfunction: Study 3

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device, Behavioral
Study Type: Interventional
Study Phase: Early Phase 1
SUMMARY

Vocal hyperfunction (VH) is the most commonly treated class of voice disorders by speech-language pathologists and voice therapy is the primary curative treatment. Patients and clinicians report that generalizing improved voicing into daily life is the most significant barrier to successful therapy. We will test if extending biofeedback into the patient's daily life using ambulatory voice monitoring will significantly improve generalization during therapy and if individual patient factors, like how easily they can modify their voice and engagement during therapy, moderate the effects of the biofeedback.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Diagnosis of vocal fold nodules and polyps.

• Secondary diagnosis of laryngopharyngeal reflux (LPR) or gastro-esophageal reflux disease (GERD)

• Secondary diagnoses commonly associated with phonotrauma like erythema, edema, varies, ectasia, laryngitis, secondary/reactive muscle tension dysphonia (MTD), hemorrhage, etc.

• Diagnosis of primary MTD.

• Allowable secondary diagnoses are LPR and GERD.

Locations
United States
Massachusetts
Boston Medical Center
RECRUITING
Boston
Massachusetts General Hospital
RECRUITING
Boston
Contact Information
Primary
Jarrad Van Stan, PhD, CCC-SLP
jvanstan@mgh.harvard.edu
617-643-8410
Backup
Robert Hillman, PhD, CCC-SLP
617-643-2466
Time Frame
Start Date: 2024-03-01
Estimated Completion Date: 2029-04-01
Participants
Target number of participants: 100
Treatments
Experimental: Conversation Training Therapy with Ambulatory Voice Biofeedback
Conversation Training Therapy will be administered one time per week for 1 hour. Ambulatory Voice Monitoring with Biofeedback will be administered during the second therapy session and for 5 days between the second and third therapy sessions.
Active_comparator: Conversation Training Therapy alone
Conversation Training Therapy will be administered one time per week for 1 hour.
Related Therapeutic Areas
Sponsors
Collaborators: Emory University, Boston Medical Center
Leads: Massachusetts General Hospital

This content was sourced from clinicaltrials.gov