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).

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

227 participants

Primary outcome timeframe

Baseline and 8 weeks

Results posted on

2026-05-11

Participant Flow

Participant milestones

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

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

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 weeks

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).

Outcome measures

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 weeks

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).

Outcome measures

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 weeks

Will 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

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 weeks

The 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

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 weeks

The 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

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 weeks

International 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

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Controls

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Suzan Abdelhalim

VDORD or local VA medical center

Phone: 608-268-1901

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place