Last updated: 02/08/2019 18:50:19
Discrete Choice Experiment in Severe Asthma
GSK study ID
205816
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Other
Other
Trial overview
Official title: Discrete Choice Experiment in Severe Asthma
Trial description: With increasing treatment options such as Mepolizumab and Omalizumab for severe asthma, there is an increasing need for identification and assessment of subject preferences to improve medication adherence. Therefore the aim of this study is to determine severe asthma subject preference for various treatment attributes like mode of administration, frequency of dosing, willingness to pay, effectiveness, safety using Discrete Choice Experiment (DCE) methodology. DCE is a type of preference study which asks subjects to make a choice between different attributes of importance in the form of a questionnaire. There are 3 stages in design of DCE and after completing all 3 stages, subject preference attributes to be studied will be selected and the DCE subject questionnaire will be developed. In the survey, subjects will be presented with discrete choice between scenarios and will be asked which one they would choose. It is expected that between 30 and 40 subjects with severe persistent asthma will participate in the final online survey from each country (N= ~150-200).
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Identification of severe asthma subject preference
Timeframe: Single time point
Estimation of the relative importance of each attribute
Timeframe: Single time point
Evaluation of a preference weight for each level of the attribute
Timeframe: Single time point
Evaluation of willingness to pay by subjects
Timeframe: single time point
Secondary outcomes:
Not applicable
Interventions:
Enrollment:
0
Primary completion date:
2018-04-05
Observational study model:
Cohort
Time perspective:
Cross-Sectional
Clinical publications:
Not applicable
- Inclusion Criteria:
- Subject with severe persistent asthma will be included in this analysis.
Inclusion and exclusion criteria
Inclusion criteria:
- Inclusion Criteria:
- Subject with severe persistent asthma will be included in this analysis.
- Subjects from multinational clinical sites which participated in the IDEAL study will be included.
- Subjects with informed consent will be included.
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
No study documents available.
Results overview
No study documents available
Recruitment status
Other
Actual primary completion date
Not applicable
Actual study completion date
Not applicable
Plain language summaries
Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.
Additional information about the trial
Not applicable
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