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i-BiSSkApp for Swallowing Rehabilitation in Parkinson's Disease

Primary Purpose

Parkinson Disease

Status
Not yet recruiting
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
i-BiSSkApp (tablet application) with swallowing therapy
Traditional behavioral swallowing therapy
Sponsored by
University of South Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson Disease

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of PD by a fellowship trained movement disorders neurologist Able to provide informed consent. Older than 18 years of age. Evidence of oropharyngeal swallowing deficits as determined during a standard of care MBSS. Exclusion Criteria: Show evidence of cognitive impairment prohibiting completion of self-informed consent. Have a history of stroke or other traumatic brain injury. Have a history of previous dysphagia treatment.

Sites / Locations

  • Univerity of South Florida

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

i-BiSSkApp Group

Traditional Treatment

Arm Description

This group will complete daily swallowing behavioral exercises with simultaneous at-home sEMG biofeedback using a tablet application. Participants will participate in weekly clinic visits and at-home therapy for 12 weeks.

This group will receive traditional swallowing therapy once a week for 12 weeks using standard therapy practices. They will also complete at-home daily practice of these exercises.

Outcomes

Primary Outcome Measures

Penetration Aspiration Scale Score (PAS)
8 point ordinal scale to assess swallowing safety.
Penetration Aspiration Scale Score (PAS)
8 point ordinal scale to assess swallowing safety.
Total Pharyngeal Residue
This is the amount of residue within the valleculae and piriform sinuses after the completion of a swallow.
Total Pharyngeal Residue
This is the amount of residue within the valleculae and piriform sinuses after the completion of a swallow.

Secondary Outcome Measures

Eating Assessment Tool-10 (EAT-10)
Validated quality of life measure of swallowing function.
Eating Assessment Tool-10 (EAT-10)
Validated quality of life measure of swallowing function.

Full Information

First Posted
April 6, 2023
Last Updated
April 19, 2023
Sponsor
University of South Florida
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1. Study Identification

Unique Protocol Identification Number
NCT05837520
Brief Title
i-BiSSkApp for Swallowing Rehabilitation in Parkinson's Disease
Official Title
At-Home Skill Training Using Biofeedback for Swallowing Rehabilitation in Parkinson's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 15, 2023 (Anticipated)
Primary Completion Date
May 31, 2024 (Anticipated)
Study Completion Date
May 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of South Florida

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Aspiration pneumonia due to dysphagia is a leading cause of death in Parkinson's disease (PD). Dysphagia intervention in the United States involves evaluation at onset of dysphagia symptoms followed by short-term therapy. Traditional therapy relies on verbal instruction and low-tech at-home exercise regimens without visual biofeedback; lacking a monitoring of accuracy or strength of exercise. Available biofeedback is office-based, bulky and expensive, thus, not readily used. The Biofeedback in Strength and Skill Training (BiSSKit) is a well-researched office based biofeedback system that has recently been converted into an affordable and accessible home-based application. This study aims to investigate the impact of swallowing therapy using the BiSSKit app on airway protective outcomes in patients with PD. Thirty participants with PD and dysphagia will be recruited for this study. Participants will undergo a baseline-modified barium swallowing (MBS) evaluation followed by 12 weekly sessions of swallowing therapy. Participants will be randomized to two swallowing therapy groups (1) traditional (2) BiSSKit app. Participants will undergo MBS following therapy completion. Outcome measures include swallowing safety, pharyngeal kinematics, and swallowing-related quality of life. We hypothesize that use of the BiSSKit will result in improved swallowing function compared to the traditional swallowing therapy group.
Detailed Description
Dysphagia, or disordered swallowing, is prevalent in almost all neurodegenerative conditions and results in the inability to effectively protect the lower airways from foreign (i.e., food/liquid) and endogenous (i.e., saliva) material [1-3]. An unfortunate consequence of dysphagia is aspiration pneumonia, which is a leading cause of death in Parkinson's disease (PD) [4-6]. Swallowing therapy has proven to be effective for the management of dysphagic symptoms in PD. Treatment is most often delivered in clinics once/week over short time periods with the expectation that exercises be completed at-home. However, these paradigms lack biofeedback to assess the accuracy and strength of the prescribed exercise and accountability to ensure completion of the exercise program. Without biofeedback or options for long-term therapeutic intervention at-home, patients often regress to baseline levels [7-9]. The proposed research project seeks to test the effectiveness of a novel at-home surface electromyography (sEMG) biofeedback therapy tool called Biofeedback in Strength and Skill Training (BiSSKit) on swallowing safety and efficiency in patients with PD. The significance of this project lies in the fact that dysphagia is expensive in terms of patient quality of life, health outcomes, and healthcare costs [10, 11] often increasing hospital costs by approximately 40% [12]. Thus, a targeted swallowing therapy system with biofeedback that can be utilized at-home may reduce hospitalizations secondary to dysphagia, help maintain therapeutic gains, and reduce the burden that dysphagia places on our healthcare system. sEMG is a therapy tool that has been used in rehabilitation practice for decades. Use of sEMG during swallowing therapy involves placement of electrodes under the chin (overlying the anterior belly of the digastric, mylohyoid and geniohyoid muscles) [13]. While the patient completes a swallowing task, electrodes detect collective muscle contractions associated with hyolaryngeal excursion - a biomechanical event critically important to airway safety and swallowing efficiency [14]. The patient can then see the waveform of the swallow displayed on a computer monitor. Measures of swallowing "strength" are derived from the amplitude of the waveform. sEMG hardware and associated software available in the marketplace today is cost prohibitive and thus, in the United States, only available for office-based swallowing intervention. sEMG provides external biofeedback regarding swallowing parameters by activating neural networks controlling both motor execution and imagery of the act of swallowing including the pre- and postcentral gyrus, inferior frontal gyrus, basal ganglia, insula, and cerebellum [15]. Research has shown that exercise programs incorporating biofeedback promote significant physiologic change that is maintained over time in patients with dysphagia [14, 16-18]. Patients with PD benefit greatly from biofeedback exercises for respiratory muscle strength and lingual strengthening programs and have even been found to maintain the gains made in therapy with at-home programs [7, 16, 19]. A limitation of the currently available sEMG programs is that research studies have solely focus on the strength aspects of the swallowing (amplitude of the waveform) while failing to address the dynamic, skill-based parameters such as timing and volitional initiation that is captured in waveform morphology. Skill based swallowing training focuses on the precision of movements; and this is especially important for patients with PD [14]. Additionally, traditional sEMG systems in the US lack the ability for clinicians to modulate swallowing targets during tasks, which, according to principles of neuroplasticity, is essential for maximizing therapeutic results. The BiSSKit program is a well-researched office-based biofeedback system that adheres to principles of neuroplasticity and incorporates skill training in addition to strength training [14]. Developed in New Zealand and recently approved by the US FDA, this program has been converted into an affordable and accessible home-based application for tablet computers. This hybrid BiSSKiT system incorporates clinical visits and home-based skill/strength training and shows promise to change current therapy delivery models. Although exciting, there is a paucity of data regarding the use of the BiSSKiT with daily home therapy focused on strength and skill based swallowing training on changes to swallowing safety and efficiency in people with PD. This study seeks to evaluate the impact of this device on swallowing outcomes compared to traditional swallowing therapy models in PD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
i-BiSSkApp Group
Arm Type
Experimental
Arm Description
This group will complete daily swallowing behavioral exercises with simultaneous at-home sEMG biofeedback using a tablet application. Participants will participate in weekly clinic visits and at-home therapy for 12 weeks.
Arm Title
Traditional Treatment
Arm Type
Active Comparator
Arm Description
This group will receive traditional swallowing therapy once a week for 12 weeks using standard therapy practices. They will also complete at-home daily practice of these exercises.
Intervention Type
Device
Intervention Name(s)
i-BiSSkApp (tablet application) with swallowing therapy
Intervention Description
The device, "International Biofeedback Strength and Skill App (i-BiSSkApp)" is an at-home swallowing biofeedback tool (hardware and software) to target rehabilitation of both skill and strength of swallowing function. The program utilizes submental surface electromyography coupled with a user-friendly interface to display visual feedback of swallowing strength and timing.
Intervention Type
Behavioral
Intervention Name(s)
Traditional behavioral swallowing therapy
Intervention Description
Participants will receive standard behavioral swallowing exercises based on the results of a swallowing evaluation. Participants will complete daily at-home exercises with written and verbal instructions and return weekly to clinic for 12 weeks of therapy.
Primary Outcome Measure Information:
Title
Penetration Aspiration Scale Score (PAS)
Description
8 point ordinal scale to assess swallowing safety.
Time Frame
Baseline
Title
Penetration Aspiration Scale Score (PAS)
Description
8 point ordinal scale to assess swallowing safety.
Time Frame
Post-12 weeks of intervention
Title
Total Pharyngeal Residue
Description
This is the amount of residue within the valleculae and piriform sinuses after the completion of a swallow.
Time Frame
Baseline
Title
Total Pharyngeal Residue
Description
This is the amount of residue within the valleculae and piriform sinuses after the completion of a swallow.
Time Frame
Post-12 weeks of intervention
Secondary Outcome Measure Information:
Title
Eating Assessment Tool-10 (EAT-10)
Description
Validated quality of life measure of swallowing function.
Time Frame
Baseline
Title
Eating Assessment Tool-10 (EAT-10)
Description
Validated quality of life measure of swallowing function.
Time Frame
Post-12 weeks of intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of PD by a fellowship trained movement disorders neurologist Able to provide informed consent. Older than 18 years of age. Evidence of oropharyngeal swallowing deficits as determined during a standard of care MBSS. Exclusion Criteria: Show evidence of cognitive impairment prohibiting completion of self-informed consent. Have a history of stroke or other traumatic brain injury. Have a history of previous dysphagia treatment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stephanie A Watts, PhD
Phone
813-821-8012
Email
srandall1@usf.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Alex Brandimore, PhD
Phone
813-974-9844
Email
abrandimore@usf.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephanie Watts, PhD
Organizational Affiliation
University of South Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
Univerity of South Florida
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stephanie Watts, PhD
Phone
813-821-8012
Email
srandall1@usf.edu

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Individual participant data that underlie results reported in an article, after deidentification (text, tables, figures, and appendices). No specific data will be shared outside of study investigators.
Citations:
PubMed Identifier
30652513
Citation
Tabor-Gray LC, Gallestagui A, Vasilopoulos T, Plowman EK. Characteristics of impaired voluntary cough function in individuals with amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener. 2019 Feb;20(1-2):37-42. doi: 10.1080/21678421.2018.1510011. Epub 2019 Jan 17.
Results Reference
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PubMed Identifier
12970031
Citation
Ebihara S, Saito H, Kanda A, Nakajoh M, Takahashi H, Arai H, Sasaki H. Impaired efficacy of cough in patients with Parkinson disease. Chest. 2003 Sep;124(3):1009-15. doi: 10.1378/chest.124.3.1009.
Results Reference
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PubMed Identifier
11222795
Citation
Smith Hammond CA, Goldstein LB, Zajac DJ, Gray L, Davenport PW, Bolser DC. Assessment of aspiration risk in stroke patients with quantification of voluntary cough. Neurology. 2001 Feb 27;56(4):502-6. doi: 10.1212/wnl.56.4.502.
Results Reference
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PubMed Identifier
14639673
Citation
Fall PA, Saleh A, Fredrickson M, Olsson JE, Granerus AK. Survival time, mortality, and cause of death in elderly patients with Parkinson's disease: a 9-year follow-up. Mov Disord. 2003 Nov;18(11):1312-6. doi: 10.1002/mds.10537.
Results Reference
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PubMed Identifier
24933728
Citation
Troche MS, Rosenbek JC, Okun MS, Sapienza CM. Detraining outcomes with expiratory muscle strength training in Parkinson disease. J Rehabil Res Dev. 2014;51(2):305-10. doi: 10.1682/JRRD.2013.05.0101.
Results Reference
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PubMed Identifier
22365489
Citation
Crary MA, Carnaby GD, LaGorio LA, Carvajal PJ. Functional and physiological outcomes from an exercise-based dysphagia therapy: a pilot investigation of the McNeill Dysphagia Therapy Program. Arch Phys Med Rehabil. 2012 Jul;93(7):1173-8. doi: 10.1016/j.apmr.2011.11.008. Epub 2012 Feb 25.
Results Reference
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PubMed Identifier
15383945
Citation
Crary MA, Carnaby Mann GD, Groher ME, Helseth E. Functional benefits of dysphagia therapy using adjunctive sEMG biofeedback. Dysphagia. 2004 Summer;19(3):160-4. doi: 10.1007/s00455-004-0003-8.
Results Reference
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PubMed Identifier
24816250
Citation
Athukorala RP, Jones RD, Sella O, Huckabee ML. Skill training for swallowing rehabilitation in patients with Parkinson's disease. Arch Phys Med Rehabil. 2014 Jul;95(7):1374-82. doi: 10.1016/j.apmr.2014.03.001. Epub 2014 May 9.
Results Reference
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PubMed Identifier
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Citation
Jenks J, Pitts LL. Effects of an Intensive Exercise-Based Swallowing Program for Persons With Parkinson's Disease and Complex Medical History: A Single-Case Experiment. Am J Speech Lang Pathol. 2019 Aug 9;28(3):1268-1274. doi: 10.1044/2019_AJSLP-18-0168. Epub 2019 Jul 23.
Results Reference
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i-BiSSkApp for Swallowing Rehabilitation in Parkinson's Disease

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