NCT00721513 · OUTCOME
MD Anderson Dysphagia Inventory
Docetaxel, Cisplatin, and Fluorouracil Followed By Cetuximab and Radiation Therapy in Treating Patients With Locally Advanced Head and Neck Cancer · Source last updated 2020-04-07
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEAN
- Unit
- Score on a scale
- Interval / dispersion
- Standard Deviation
- Time frame
- Baseline, pre-radiation therapy and post-radiation therapy, up to 2 years
What was measured
The MD Anderson Dysphasia Inventory (MDADI) is a survey specifically designed to assess dysphasia. It contains 20 questions directly addressing the swallowing function and several other general questions. The questionnaire asks for participants views about their swallowing ability at baseline, pre-radiation therapy and post-radiation therapy. All questions except for E7 and F2: Strongly Agree = 1 point, Agree = 2 points, No Opinion = 3 points, Disagree = 4 points, Strongly Disagree. E7 and F2: Strongly agree = 5 points, Agree = 4 points, no opinion = 3 points, disagree = 2 points, strongly disagree = 1 point. Scores range from 20 (extremely low-functioning) to 100 (high-functioning).
Analysis population: Data was not collected on all participants
Groups in this outcome
TPFChemotherapy + Concomitant Cetuximab & RT
Taxotere/Cisplatinum/5-Fluorouracil (TPF) Chemotherapy Followed by Concomitant Cetuximab \& Radiation Therapy
cetuximab
cisplatin
docetaxel
fluorouracil
computed tomography
positron emission tomography
quality-of-life assessment
3-dimensional conformal radiation therapy
intensity-modulated radiation therapy
Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 10 |
|---|
Reported measurements
Baseline Global Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 10 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 56.00 | 32.39 | Not reported | Not reported | Not reported |
|---|
Baseline Emotion Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 9 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 71.48 | 16.68 | Not reported | Not reported | Not reported |
|---|
Baseline Function Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 9 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 75.56 | 20.34 | Not reported | Not reported | Not reported |
|---|
Baseline Physical Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 10 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 68.00 | 22.94 | Not reported | Not reported | Not reported |
|---|
Pre-RT Global Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 5 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 88.00 | 26.83 | Not reported | Not reported | Not reported |
|---|
Pre-RT Emotion Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 5 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 83.07 | 6.35 | Not reported | Not reported | Not reported |
|---|
Pre-RT Function Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 5 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 76.80 | 9.96 | Not reported | Not reported | Not reported |
|---|
Pre-RT Physical Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 5 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 86.00 | 19.89 | Not reported | Not reported | Not reported |
|---|
Post-RT Global Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 8 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 62.50 | 36.15 | Not reported | Not reported | Not reported |
|---|
Post-RT Emotion Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 8 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 67.08 | 17.59 | Not reported | Not reported | Not reported |
|---|
Post-RT Function Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 7 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 58.29 | 26.62 | Not reported | Not reported | Not reported |
|---|
Post-RT Physical Score
Analysis denominator · Participants
| Group | Source count |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 8 |
|---|
Values in Score on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| TPFChemotherapy + Concomitant Cetuximab & RT | 67.81 | 26.47 | Not reported | Not reported | Not reported |
|---|
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- spread
- 32.39
- value
- 56.00
- title
- Baseline Global Score
- categories
- measurements
- group Id
- OG000
- spread
- 16.68
- value
- 71.48
- title
- Baseline Emotion Score
- categories
- measurements
- group Id
- OG000
- spread
- 20.34
- value
- 75.56
- title
- Baseline Function Score
- categories
- measurements
- group Id
- OG000
- spread
- 22.94
- value
- 68.00
- title
- Baseline Physical Score
- categories
- measurements
- group Id
- OG000
- spread
- 26.83
- value
- 88.00
- title
- Pre-RT Global Score
- categories
- measurements
- group Id
- OG000
- spread
- 6.35
- value
- 83.07
- title
- Pre-RT Emotion Score
- categories
- measurements
- group Id
- OG000
- spread
- 9.96
- value
- 76.80
- title
- Pre-RT Function Score
- categories
- measurements
- group Id
- OG000
- spread
- 19.89
- value
- 86.00
- title
- Pre-RT Physical Score
- categories
- measurements
- group Id
- OG000
- spread
- 36.15
- value
- 62.50
- title
- Post-RT Global Score
- categories
- measurements
- group Id
- OG000
- spread
- 17.59
- value
- 67.08
- title
- Post-RT Emotion Score
- categories
- measurements
- group Id
- OG000
- spread
- 26.62
- value
- 58.29
- title
- Post-RT Function Score
- categories
- measurements
- group Id
- OG000
- spread
- 26.47
- value
- 67.81
- title
- Post-RT Physical Score
- description
- The MD Anderson Dysphasia Inventory (MDADI) is a survey specifically designed to assess dysphasia. It contains 20 questions directly addressing the swallowing function and several other general questions. The questionnaire asks for participants views about their swallowing ability at baseline, pre-radiation therapy and post-radiation therapy. All questions except for E7 and F2: Strongly Agree = 1 point, Agree = 2 points, No Opinion = 3 points, Disagree = 4 points, Strongly Disagree. E7 and F2: Strongly agree = 5 points, Agree = 4 points, no opinion = 3 points, disagree = 2 points, strongly disagree = 1 point. Scores range from 20 (extremely low-functioning) to 100 (high-functioning).
- dispersion Type
- Standard Deviation
- groups
- description
- Taxotere/Cisplatinum/5-Fluorouracil (TPF) Chemotherapy Followed by Concomitant Cetuximab \& Radiation Therapy
cetuximab
cisplatin
docetaxel
fluorouracil
computed tomography
positron emission tomography
quality-of-life assessment
3-dimensional conformal radiation therapy
intensity-modulated radiation therapy
- id
- OG000
- title
- TPFChemotherapy + Concomitant Cetuximab & RT
- param Type
- MEAN
- population Description
- Data was not collected on all participants
- reporting Status
- POSTED
- time Frame
- Baseline, pre-radiation therapy and post-radiation therapy, up to 2 years
- title
- MD Anderson Dysphagia Inventory
- type
- SECONDARY
- unit Of Measure
- Score on a scale
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice