Impact of Chronic Pulmonary Aspergillosis (CPA) on Health Status and Well-being
CAPSULE
1 other identifier
observational
100
1 country
3
Brief Summary
To develop and validate a novel disease-specific questionnaire for measuring HRQoL in patients with Chronic Pulmonary Aspergillosis (CPA-HAQ) for use in clinical research, including clinical trials.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Nov 2024
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 27, 2024
CompletedFirst Submitted
Initial submission to the registry
March 13, 2025
CompletedFirst Posted
Study publicly available on registry
March 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 23, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 23, 2026
CompletedMarch 20, 2025
March 1, 2025
9 months
March 13, 2025
March 13, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Impact of Chronic Pulmonary Aspergillosis (CPA) on health status and Well-being.
To develop and validate a novel disease-specific health-related quality of life (HRQoL) measure in chronic pulmonary aspergillosis (CPA): The Chronic Pulmonary Aspergillosis Health Assessment Questionnaire (CPA-HAQ)
30 months
Secondary Outcomes (2)
Impact of Chronic Pulmonary Aspergillosis (CPA) on health status and Well-being.
30 months
Impact of Chronic Pulmonary Aspergillosis (CPA) on health status and Well-being.
30 months
Eligibility Criteria
Individuals with confirmed Chronic Pulmonary Aspergillosis
You may qualify if:
- All patients \>/= 18 years old and able to provide informed consent
- Patients with a diagnosis of chronic pulmonary aspergillosis
- To speak and understand English
- Able to provide informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Imperial College Londonlead
- Manchester University NHS Foundation Trustcollaborator
- Tayside Medical Science Centrecollaborator
Study Sites (3)
Ninewells Hospital & Medical School
Dundee, DD1 9SY, United Kingdom
Imperial College London
London, United Kingdom
Manchester NHS Foundation Trust
Manchester, United Kingdom
Related Links
Biospecimen
Blood and sputum
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 13, 2025
First Posted
March 20, 2025
Study Start
November 27, 2024
Primary Completion
August 23, 2025
Study Completion
April 23, 2026
Last Updated
March 20, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share