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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03349086
Other study ID # 2013-1746
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 28, 2014
Est. completion date July 25, 2018

Study information

Verified date May 2019
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the effect of voice exercise and voice rest on subject's perception of vocal handicap and communicative participation following Botox injections for adductor spasmodic dysphonia.


Description:

Spasmodic dysphonia (SD) is a neurological disorder characterized by involuntary spasms of the vocal folds resulting in a strained and strangled voice quality. This disorder is quite disabling to patients who suffer from it, particularly affecting patients' quality of life. Botulinum toxin (Botox) has been found to be the most effective treatment for SD. The Botox is injected into the affected muscle resulting in temporary weakening of the muscle. The patients return for injections on average every 3 - 6 months.

There is a suggestion in the literature that increased diffusion of the Botox injectate could improve the effects of the injection. Furthermore, there is literature supporting the use of exercise to increase the diffusion of the Botox. Previous research examined the use of voluntary muscle activity vs. rest immediately following Botox injection for writer's cramp. It was found that the active condition resulted in greater reduction of muscle strength in the injected muscle. Another small study of 9 patients implemented intense exercise comprised of loud reading for one hour and a rest condition of total voice rest for 24 hours. They found that the exercise condition resulted in improved scores on the voice related-quality of life (V-RQOL) measure and concluded that improvement in results of Botox injections may be achieved more consistently with the implementation of exercise following the injection. The exercise used in this study was intense and may be contrary to the overall benefit as the subjects may experience phonotrauma. Timing of the exercise post-injection may also be a factor. Previous literature review revealed combined modality treatment of Botox injection only, Botox with therapy and Botox with sham treatment. They found no significant differences in acoustic stability, V-RQOL, or duration of injection benefit. However, the exercise was initiated 3 weeks post-injection and completed once per week for 5 weeks. Investigators aim to identify what might improve or extend the duration of botox injections for adductor Spasmodic dysphonia.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date July 25, 2018
Est. primary completion date July 25, 2018
Accepts healthy volunteers No
Gender Female
Age group 21 Years to 70 Years
Eligibility Inclusion Criteria:

1. Female

2. 21-70 age

3. Diagnosed with pure adductor spasmodic dysphonia

4. Completed 2 consecutive standard of care Botox injection into the thyroarytenoid (TA) and/or thyroarytenoid/lateral cricoarytenoid (TA/LCA) junction with the same dosage

Exclusion Criteria:

1. Receiving Botox to other laryngeal or supraglottic musculature

2. Other neuro-laryngological conditions

3. Those with an average of less than two injections per year

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Voice Exercise
Voice exercise will consist of sustained pitches and pitch glides on a variety of different vocal facilitators.

Locations

Country Name City State
United States University of Wisconsin - Madison Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary A quantifiable difference between the effects of voice exercise vs. voice rest post Adductor Spasmodic Dysphonia botox treatment through analysis of the Voice Handicap Index Questionnaire. Pre randomized condition and post 6 week and 12 week, participants will be asked to complete the Voice Handicap Index (VHI).
The VHI Questionnaire (Voice Handicap Index) is a 30-item questionnaire divided into 3 subsections (Functional, Physical, Emotional) and a Total which measures the effect of voice problems on quality of life. Individuals mark each item on this 30-item questionnaire on a scale from 0-4 (0 being never and 4 being always). Points for each subscale are tallied and a total composite score is also given. A total score of 0-11 is considered Normal, 12-28 is considered Mild Minimal handicap, 29-56 is considered Moderate Handicap, and 57-120 is considered severe handicap.
Assessing the change of the post VHI questionnaire between groups. Data will be reported at study completion, an average of 1 year.
See also
  Status Clinical Trial Phase
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Enrolling by invitation NCT03129087 - The Effect of Vocal Rest Versus Vocalization Following Xeomin® Injections in Spasmodic Dysphonia N/A
Not yet recruiting NCT06402214 - The 'Lombard Effect' in Patients Affected by Adductor Laryngeal Dystonia N/A
Completed NCT02528006 - Treatment for Adductor Spasmodic Dysphonia by Type 2 Thyroplasty Using Titanium Bridges Phase 2/Phase 3
Not yet recruiting NCT05467228 - Laryngeal Vibro-tactile Stimulation as a Non-invasive Symptomatic Treatment for Spasmodic Dysphonia Phase 2
Completed NCT05158179 - Assessment of Laryngopharyngeal Sensation in Adductor Spasmodic Dysphonia N/A