- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04410120
Impact of Asthma Exacerbations (IMPAX)
Impact of Asthma Exacerbations: A Qualitative Study
The purpose of the study is to gain a deeper understanding of the impact of asthma attacks on the lives of patients who experience them. This will help us to describe the true extent of the impact of asthma attacks on factors of importance to patients which have not previously been well described, including the psychological, social, financial and emotional burden of asthma attacks.
Additionally, it is hoped that detailed questioning regarding features of asthma attacks from a patient perspective will improve our understanding of patient recognition of attacks, consistency of certain features of attacks and patient views regarding preventative strategies for attacks. Patient experiences of asthma attacks are poorly described in previous research. Hence this work is expected to provide useful insights into these experiences which will contribute to improvements in detecting, treating and preventing asthma attacks.
The study will consist of a one-off interview lasting about 45 minutes with patients who have recently had asthma attacks. We plan to recruit patients for the study from an outpatient clinic for those who have had a recent attack or from a register of patients who have volunteered for future asthma research studies. The interviews will take place in person at the Respiratory Research Unit at the Nottingham City Hospital or over the telephone depending on patient preference.
Study Overview
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
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Nottinghamshire
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Nottingham, Nottinghamshire, United Kingdom, NG5 1PB
- Nottingham Respiratory Research Unit
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Contact:
- Matthew J Martin, PhD, MBChB
- Email: matthew.martin@nottingham.ac.uk
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Principal Investigator:
- Matthew J Martin, PhD, MBChB
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Sub-Investigator:
- Manpreet Bains, PhD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults with previous clinician diagnosis of asthma (16 years and above)
- Recent (≤4 weeks) asthma attack for which patient received ≥3 days of systemic corticosteroid treatment
Exclusion Criteria:
- Anyone under the age of 16 years.
- Anyone unable to speak or understand English.
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Asthma with recent (<4/52) asthma attack
|
Semi-structured 45 minute interviews regarding impact of asthma attacks
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Thematic analysis of interview transcripts using framework approach
Time Frame: One off 45 minute interview
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Thematic analysis of interview transcripts using framework approach
|
One off 45 minute interview
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20038
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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