FF/UMEC/VI Inhaler: Qualitative Analysis and Subject Preference Survey

GlaxoSmithKline634 enrolled

Overview

Three main classes of inhaled treatment exist for chronic obstructive pulmonary disease (COPD): Beta2-adrenergic agonists (which may be short (SABA) or long (LABA) acting), long-acting muscarinic acetylcholine receptor antagonists (LAMA), and inhaled corticosteroids (ICS). For subjects at higher risk of exacerbation, treatment with all these three classes of medication is recommended. This study aims to explore the potential utility of a device called single inhaler triple combination or fluticasone furoate/ umeclidinium/ vilanterol (FF/UMEC/VI) inhaler containing all three groups of compound. This is a mixed methods study with a qualitative phase and a quantitative Discrete Choice Experiment (DCE) phase and will be conducted in four stages: qualitative concept elicitation, DCE development, DCE piloting and testing, and conduct of the DCE. The study will conducted in the United Kingdom (UK), United States (US) and Germany and approximately 573 subjects with COPD will be included.

Study Type

OBSERVATIONAL

Enrollment

634

Conditions

Pulmonary Disease, Chronic Obstructive

Interventions

Telephone interviewsOTHER

Qualitative concept elicitation telephone interviews will be conducted in subjects with COPD to explore treatment effectiveness, symptoms, quality of life, and features of treatment that are considered to be most important to them when making treatment choices.

In-person focus groupsOTHER

Qualitative concept elicitation in-person focus groups will be conducted in subjects with COPD to explore treatment effectiveness, symptoms, quality of life, and features of treatment that are considered to be most important to them when making treatment choices.

DCE surveys- cognitive interviewsOTHER

Draft version of the DCE surveys will be tested with subjects in cognitive interviews to explore the saliency of the attribute choices and assess whether the attributes are understandable, meaningful and comprehensive.

Modified DCEOTHER

The modified DCEs will be piloted with subjects with COPD in each country to refine the underlying design and ensure that information is collected in an efficient way to enable the statistical analysis to be as precise as possible.

Online DCE surveyOTHER

An online DCE survey questionnaire will be given to the subjects to identify subject preferences, priorities and treatment goals.

Eligibility

Sex: ALLMin age: 40 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Diagnosis of COPD, self-reported. * Age: More than or equal to 40 years. * Moderate to severe COPD, indicated by a COPD Assessment Test (CAT) score of greater than or equal to 10 or Modified Medical Research Council (MMRC) score of greater than or equal to 2. * Currently prescribed and receiving one of the following treatment types: ICS/LABA; LABA/LAMA; ICS/LABA/LAMA (triple therapy); LAMA. * Currently resident in the UK, US or Germany. * Adequate written and oral fluency in language of country of residence. * Willing and able to understand the study and provide informed consent. * Has access to the internet (Cognitive interviews and DCE survey only). Exclusion Criteria: * Has taken part in any other stage of this study. * Subjects with a current diagnosis of asthma. (Subjects with a prior history of asthma are eligible if they have a current diagnosis of COPD). * Any co-morbidity that would inhibit the ability to provide informed consent or allow participation in a telephone of face-to-face interview.

Locations (1)

GSK Investigational Site

London, United Kingdom

Outcomes

Primary Outcomes

Evaluation of the key relevant attributes of COPD treatment

The key attributes considered to be most important to subjects with COPD when making treatment choices will be assessed using the data from the subject interviews and focus groups.

Time frame: Up to 368 hours

Evaluation of the preferences, priorities and treatment goals of subjects with COPD for inhaled treatments

The probability of choosing one treatment over another will be evaluated using DCE survey questionnaire.

Time frame: Up to 368 hours

Secondary Outcomes

Assessment of the relative appeal of different treatment approaches

The burden of COPD, priorities in terms of symptoms and treatment effect, goals and preferences of subjects will be analyzed.

Time frame: Up to 371 hours

Estimation of the relative importance of each attribute

The DCE online survey will be used to assess the relative importance of treatment attributes and priorities.

Time frame: Up to 371 hours

Data from ClinicalTrials.gov

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