Trial Outcomes & Findings for Novel Pharyngeal Metrics to Predict Dysphagia Outcomes (NCT NCT04569097)
NCT ID: NCT04569097
Last Updated: 2026-05-11
Results Overview
Will assess the change in pressure by pharyngeal high resolution manometry over the time frame. The primary measure of interest is Integral Pressure during the 10 mL swallow at the tongue base. This is measured in two forms: 1\. Pharyngeal Contractile Integral (PhCI): range is between 100 and 600 mmHg·s·cm ; 2. Mesopharyngeal Max Pressure (tongue base): range is between \~115-210 mmHg in healthy adults. Positive change would be a movement toward normal range of pressure. This metric is measured automatically in both Software systems used to evaluate pharyngeal pressure (WiscMano and Swallow gateway).
COMPLETED
NA
227 participants
Baseline and 8 weeks
2026-05-11
Participant Flow
Participant milestones
| Measure |
Patient Group
lingual strengthening
|
Controls
No history of dysphagia (swallowing disorder) or minimal to mild dysphagia not requiring a strengthening program
|
|---|---|---|
|
Overall Study
STARTED
|
112
|
115
|
|
Overall Study
COMPLETED
|
79
|
75
|
|
Overall Study
NOT COMPLETED
|
33
|
40
|
Reasons for withdrawal
| Measure |
Patient Group
lingual strengthening
|
Controls
No history of dysphagia (swallowing disorder) or minimal to mild dysphagia not requiring a strengthening program
|
|---|---|---|
|
Overall Study
Withdrawal by Subject
|
33
|
40
|
Baseline Characteristics
Novel Pharyngeal Metrics to Predict Dysphagia Outcomes
Baseline characteristics by cohort
| Measure |
Patient Group
n=112 Participants
lingual strengthening
|
Controls
n=115 Participants
No history of dysphagia (swallowing disorder) or minimal to mild dysphagia not requiring a strengthening program
|
Total
n=227 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=44 Participants
|
0 Participants
n=10 Participants
|
0 Participants
n=30 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
29 Participants
n=44 Participants
|
61 Participants
n=10 Participants
|
90 Participants
n=30 Participants
|
|
Age, Categorical
>=65 years
|
83 Participants
n=44 Participants
|
54 Participants
n=10 Participants
|
137 Participants
n=30 Participants
|
|
Sex: Female, Male
Female
|
2 Participants
n=44 Participants
|
22 Participants
n=10 Participants
|
24 Participants
n=30 Participants
|
|
Sex: Female, Male
Male
|
110 Participants
n=44 Participants
|
93 Participants
n=10 Participants
|
203 Participants
n=30 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
1 Participants
n=44 Participants
|
1 Participants
n=10 Participants
|
2 Participants
n=30 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
108 Participants
n=44 Participants
|
113 Participants
n=10 Participants
|
221 Participants
n=30 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
3 Participants
n=44 Participants
|
1 Participants
n=10 Participants
|
4 Participants
n=30 Participants
|
PRIMARY outcome
Timeframe: Baseline and 8 weeksWill assess the change in pressure by pharyngeal high resolution manometry over the time frame. The primary measure of interest is Integral Pressure during the 10 mL swallow at the tongue base. This is measured in two forms: 1\. Pharyngeal Contractile Integral (PhCI): range is between 100 and 600 mmHg·s·cm ; 2. Mesopharyngeal Max Pressure (tongue base): range is between \~115-210 mmHg in healthy adults. Positive change would be a movement toward normal range of pressure. This metric is measured automatically in both Software systems used to evaluate pharyngeal pressure (WiscMano and Swallow gateway).
Outcome measures
| Measure |
Patient Group
n=112 Participants
lingual strengthening
|
Controls
n=115 Participants
No history of dysphagia (swallowing disorder) or minimal to mild dysphagia not requiring a strengthening program
|
|---|---|---|
|
pHRM Pressure Change (Pharyngeal)
Baseline Pharyngeal Contractile Integral
|
381 mmHg·s·cm
Standard Deviation 128
|
395 mmHg·s·cm
Standard Deviation 127
|
|
pHRM Pressure Change (Pharyngeal)
8 weeks Pharyngeal Contractile Integral
|
389 mmHg·s·cm
Standard Deviation 140
|
402 mmHg·s·cm
Standard Deviation 111
|
PRIMARY outcome
Timeframe: Baseline and 8 weeksWill assess the change in pressure by pharyngeal high resolution manometry over the time frame. The primary measure of interest is Integral Pressure during the 10 mL swallow at the tongue base. This is measured in two forms: 1\. Pharyngeal Contractile Integral (PhCI): range is between 100 and 600 mmHg·s·cm ; 2. Mesopharyngeal Max Pressure (tongue base): range is between \~115-210 mmHg in healthy adults. Positive change would be a movement toward normal range of pressure. This metric is measured automatically in both Software systems used to evaluate pharyngeal pressure (WiscMano and Swallow gateway).
Outcome measures
| Measure |
Patient Group
n=112 Participants
lingual strengthening
|
Controls
n=115 Participants
No history of dysphagia (swallowing disorder) or minimal to mild dysphagia not requiring a strengthening program
|
|---|---|---|
|
pHRM Pressure Change (Mesopharyngeal)
Baseline Mesopharyngeal Max Pressure
|
192 mmHg
Standard Deviation 73
|
185 mmHg
Standard Deviation 56
|
|
pHRM Pressure Change (Mesopharyngeal)
8 weeks Mesopharyngeal Max Pressure
|
200 mmHg
Standard Deviation 70
|
191 mmHg
Standard Deviation 61
|
PRIMARY outcome
Timeframe: Baseline and 8 weeksWill assess the change in fluoroscopy and clinical assessments over the time frame. The primary tool of measurement is the combined score of the Modified Barium Swallow Impairment Profile (MBSImP). This is a 17 item standardized tool to measure impairment of swallow identified using contrast barium swallows. The investigators will use the composite pharyngeal score which ranges from 0 to 3, the higher the score the more abnormal the swallow function, Normal swallows will score 5 or less and severe dysphagia will score 9 or higher. Movement toward 0 is a positive or improved swallow function, movement toward 23 is negative or worsening swallow function and full range is from 0 to 29 with a higher score indicating worse impairment. Scores under 13 indicate the mild or no impairment.
Outcome measures
| Measure |
Patient Group
n=112 Participants
lingual strengthening
|
Controls
n=115 Participants
No history of dysphagia (swallowing disorder) or minimal to mild dysphagia not requiring a strengthening program
|
|---|---|---|
|
Swallowing Clinical and Fluoroscopic Change (MBSImP)
Baseline MBSImP
|
10.7 score on a scale
Standard Deviation 3.2
|
6.0 score on a scale
Standard Deviation 2.4
|
|
Swallowing Clinical and Fluoroscopic Change (MBSImP)
8 weeks MBSImP
|
9.2 score on a scale
Standard Deviation 2.4
|
6.8 score on a scale
Standard Deviation 2.2
|
PRIMARY outcome
Timeframe: Baseline and 8 weeksThe Sydney Swallowing Questionnaire (SSQ) is a patient reported symptom scale with 17 questions, each scaled from 0+ no dysfunction to 100 equal extreme dysfunction using a 100mm visual analogue scale with 0 and 100 as anchors. The total score can be recorded for 0 to 1700. Normal swallowers will average 40 with a range of 200 to 0. Dysphagia patients average 800 with a range of 150 to 1600. Movement toward 0 will be considered an improvement, movement toward 1700 worsening in swallowing ability preserved by the patient.
Outcome measures
| Measure |
Patient Group
n=112 Participants
lingual strengthening
|
Controls
n=115 Participants
No history of dysphagia (swallowing disorder) or minimal to mild dysphagia not requiring a strengthening program
|
|---|---|---|
|
Patient Reported Outcome Changes (SSQ)
Baseline SSQ
|
512 score on a scale
Standard Deviation 358
|
149 score on a scale
Standard Deviation 198
|
|
Patient Reported Outcome Changes (SSQ)
8 weeks SSQ
|
377 score on a scale
Standard Deviation 309
|
164 score on a scale
Standard Deviation 185
|
SECONDARY outcome
Timeframe: Baseline and 8 weeksThe Eating Assessment Tool-10 (EAT-10) is a short 10 question swallowing assessment tool with 10 questions each scaled 0 to 4, total can be between 0 and 40. The normal swallowers will score under 2. Changes toward 0 will be identified as improved swallow symptom function, changes toward 40 worsening symptoms.
Outcome measures
| Measure |
Patient Group
n=112 Participants
lingual strengthening
|
Controls
n=115 Participants
No history of dysphagia (swallowing disorder) or minimal to mild dysphagia not requiring a strengthening program
|
|---|---|---|
|
Patient Reported Outcome Changes (EAT-10)
Baseline EAT-10
|
13.8 score on a scale
Standard Deviation 8.9
|
3.8 score on a scale
Standard Deviation 6.6
|
|
Patient Reported Outcome Changes (EAT-10)
8 weeks EAT-10
|
9.0 score on a scale
Standard Deviation 8.5
|
4.0 score on a scale
Standard Deviation 5.9
|
SECONDARY outcome
Timeframe: Baseline, 4 weeks, and 8 weeksInternational Dysphagia Diet Standardization initiative, Functional Oral Intake scale. Standardize scale of diet (liquid and solid food, iddsi.org). Foods scaled from regular diet 7 to liquidized 3, and liquids scaled from thin liquids 0 to extremely thick 4. Improvement in diet will be report if patients move toward 0 in liquid intake and toward 7 in solid food intact, and movement in the opposite directions will be evidence of poorly food and liquid tolerance.
Outcome measures
Outcome data not reported
Adverse Events
Patient Group
Controls
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place