NCT05882890 · OUTCOME
Xerostomia Questionnaire
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
- Full Range
- Time frame
- Baseline (before start of this study intervention, but at least two years after finishing treatment of cancer)
What was measured
A Danish questionnaire for following up on patients who have finished their cancer treatment in head and neck on a Danish hospital. It is used at least 3 months after treatment. The participants in this study has finished their treatment for cancer at least two years from enroling this study. VAS xerostomia scale0-10 (10 is worst) The remaining 14 questions were phrased "how much does \[question subject\] bother you:" (translated from Danish) not at all (1) - a little (2) - some (3) a lot (4) very much( 5) The final question(number 15) were: "How would you feel, if you had to live the rest of your life, with the symptoms you have now?:" enjoyable(1), very satisfied (2) neither satisfied ore unsatisfied(3), very unsatisfied(4), terrible(5) the sum of points from the 15 questions gives an overall score.
Analysis population: 11 participants entered the project. 1 participant was not analysed, because of to low score at the xerostomia vas-scale i baseline. The inclusioncriteria for entering the analysis phase of the project was a score at at least 4 n the xerostomia vas-scale
Groups in this outcome
Craniosacral Therapy Receivers
Please refer to baseline characteristics
| Group | Source count |
|---|---|
| Craniosacral Therapy Receivers | 10 |
Reported measurements
VAS scale(0best -10 worst)
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Craniosacral Therapy Receivers | 8 | Not reported | 6 | 10 | Not reported |
Remaining 15 questions overall sum (15 worst-75 best)
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Craniosacral Therapy Receivers | 46.4 | Not reported | 30 | 65 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 6
- upper Limit
- 10
- value
- 8
- title
- VAS scale(0best -10 worst)
- categories
- measurements
- group Id
- OG000
- lower Limit
- 30
- upper Limit
- 65
- value
- 46.4
- title
- Remaining 15 questions overall sum (15 worst-75 best)
- denoms
- counts
- group Id
- OG000
- value
- 10
- units
- Participants
- description
- A Danish questionnaire for following up on patients who have finished their cancer treatment in head and neck on a Danish hospital. It is used at least 3 months after treatment. The participants in this study has finished their treatment for cancer at least two years from enroling this study. VAS xerostomia scale0-10 (10 is worst) The remaining 14 questions were phrased "how much does \[question subject\] bother you:" (translated from Danish) not at all (1) - a little (2) - some (3) a lot (4) very much( 5) The final question(number 15) were: "How would you feel, if you had to live the rest of your life, with the symptoms you have now?:" enjoyable(1), very satisfied (2) neither satisfied ore unsatisfied(3), very unsatisfied(4), terrible(5) the sum of points from the 15 questions gives an overall score.
- dispersion Type
- Full Range
- groups
- description
- Please refer to baseline characteristics
- id
- OG000
- title
- Craniosacral Therapy Receivers
- param Type
- MEAN
- population Description
- 11 participants entered the project. 1 participant was not analysed, because of to low score at the xerostomia vas-scale i baseline. The inclusioncriteria for entering the analysis phase of the project was a score at at least 4 n the xerostomia vas-scale
- reporting Status
- POSTED
- time Frame
- Baseline (before start of this study intervention, but at least two years after finishing treatment of cancer)
- title
- Xerostomia Questionnaire
- type
- PRIMARY
- unit Of Measure
- score on a scale
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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