New SwallowFit exercise aims to ease Parkinson's swallowing problems
NCT ID NCT07356414
First seen Jun 25, 2026 · Last updated Jul 14, 2026 · Updated 3 times
Summary
This study tests a 6-week exercise program called SwallowFit designed to improve swallowing fitness in people with Parkinson's disease. Researchers will compare the exercise group to those receiving standard care. The goal is to see if the exercises lead to safer swallowing and better quality of life for 80 U.S. service members, veterans, and their families.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- SwallowFit exercise program (swallowing exercises)
- What this could lead to
- If it works, this could provide a simple exercise program to help people with Parkinson's swallow more safely and improve their quality of life.
- What could go wrong
- This is a small, early-stage trial with only 80 participants. The exercises may not work for everyone, and results may not apply to all Parkinson's patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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35 to 90 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Adult S-VWP between \>35-90 years of age 2. Diagnosis of Idiopathic Parkinson's Disease \[IDP\] (either or suspected, tremor-predominant or rigid predominant) 3. Disability level of Hoehn \& Yahr stages II-III as indicated in their most recent neurological evaluation 4. Swallowing concern, confirmed by Modified Unified Parkinson Disease Rating Scale \[MDS-UPDRS\]- 5. ADL swallowing item \>0, or Mann Assessment of Swallowing scale \[MASA\] score ≤185. 6. Able to consume oral nutrition \[Functional Oral Intake Score ≤ 6\] 7. Ambulatory 8. No change of medication for at least 4 weeks before study inclusion Exclusion Criteria: 1. Classified as Hoehn and Yahr stages IV 2. Unable to follow 2 step commands 3. History of other neurological disease potentially causing dysphagia 4. Dementia (MMSE\<20; Montreal cognitive assessment (MoCA) ≤ 20) 5. Severe depression (BDI\>19) 6. Severe dyskinesia of head and neck (resulting in problems with MBSS recording) 7. Severe documented Gastrointestinal disease 8. History of Gastro-esophageal surgery 9. History of Head or neck cancer with swallowing impairment or surgical intervention 10. History of breathing disorders or diseases (e.g., Asthma, chronic obstructive pulmonary disease (COPD) requiring assistive breathing support. 11. Untreated hypertension 12. Heart disease requiring restricted activity and medical intervention 13. Speech therapy intervention for swallowing within the past three months 14. Women who are pregnant, nursing, or who plan to become pregnant during the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Brooke Army Medical Center (BAMC)
San Antonio, Texas, 78234-6200, United States
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