Chronic Obstructive Pulmonary Disease (COPD) Clinical Trials

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Observational Cohort Study of Hospitalised Patients With Acute Respiratory Conditions

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The goal of this observational study is to learn about the short- and long-term outcomes of people admitted to hospital with an acute respiratory condition, including exacerbations of chronic lung disease, and to understand factors that may predict recovery, hospital readmission, length of hospital stay, and mortality. A group of people with chronic respiratory disease who are being followed in respiratory outpatient clinics and a healthy control group without lung disease will also take part. The main questions it aims to answer are: * Which clinical, physical, functional, and biological characteristics are associated with short-term outcomes after hospitalisation, including 30-day hospital readmission, length of hospital stay, and 30-day mortality? * Which characteristics are associated with longer-term recovery, future exacerbations, hospital readmissions, healthcare use, and mortality? * Can measurements taken during or around the time of hospitalisation be used to identify people at greater risk of poor outcomes who may benefit from targeted interventions? Participants will undergo clinical assessments that may include questionnaires, measurements of physical function and muscle strength, lung function tests, physical activity monitoring, and collection of biological samples. Some participants may also undergo additional assessments of body composition, muscle size and function, imaging, or muscle metabolism, including through nested sub-studies. Participants will be followed for up to 36 months to assess recovery and longer-term clinical outcomes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 90
Healthy Volunteers: t
View:

• Hospital admission with an acute respiratory diagnosis, or currently under the care of hospital respiratory outpatient services for a chronic respiratory disease

• Participant is willing \& able to give informed consent for participation in the study

• Aged 18 years or above

• Able (in the Investigators opinion) \& willing to comply with all study requirements

• Aged 18 years or above

• No underlying respiratory disease as self-reported

• Able (in the Investigators opinion) \& willing to comply with all study requirements

Locations
Other Locations
United Kingdom
Glenfield Hospital
RECRUITING
Leicester
Contact Information
Primary
Jill Clanchy
chesty-catalina@leicester.ac.uk
+44 (0)116 258 3370
Backup
Hamish McAuley, MBBS, MRCP
hjcm1@leicester.ac.uk
Time Frame
Start Date: 2022-02-02
Estimated Completion Date: 2033-10-30
Participants
Target number of participants: 500
Treatments
Hospitalised Patients
Participants admitted to hospital with an acute respiratory condition including exacerbation of an underlying physician diagnosed chronic lung disease.
Matched Controls (stable COPD and healthy volunteers)
The study will include matched controls (non-hospitalised patients with stable chronic respiratory conditions or healthy volunteers) to compare the exploratory endpoints. The number of the matched controls will not exceed 25% of the main study recruitment.
Sponsors
Leads: University of Leicester
Collaborators: University Hospitals, Leicester

This content was sourced from clinicaltrials.gov