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Interstitial Lung Disease Questionnaire

U

University of East Anglia

Status

Unknown

Conditions

Interstitial Lung Disease

Study type

Observational

Funder types

Other

Identifiers

NCT01711151
2012RESP05
UEAILDQUEST (Other Identifier)

Details and patient eligibility

About

  1. To evaluate the health status of patients with Interstitial Lung Disease (ILD), and how this varies between subgroups of ILD.
  2. To investigate the prevalence of symptoms, anxiety, depression, and sleep-disordered breathing within ILD patient population.
  3. To assess the economic impact of ILD.
  4. To understand how self-aware ILD patients are regarding their treatment/management.
  5. To compare the demographic details, including smoking status and occupational history, of patients with interstitial lung disease

Full description

Primary endpoint

• Health status in the target populations, as determined by the K-BILD questionnaire.

Secondary endpoints -

  • Severity of dyspnoea suffered by patients
  • Prevalence of anxiety and depression
  • Prevalence of sleep-disordered breathing symptoms
  • Degree of self-awareness displayed by patients
  • The costs associated with ILD from a patient and healthcare perspective.
  • Demographic details

Enrollment

304 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male or female
  • Age greater than 18 years of age
  • Any smoking status
  • Diagnosis of Interstitial Lung Disease as defined below
  • Full pulmonary lung function tests and routine immunological tests undertaken within 6 months of entry into study

Exclusion criteria

• Unable to give consent to take part

Trial design

304 participants in 4 patient groups

Idiopathic Pulmonary Fibrosis
Description:
Questionnaire evaluation
Non Idiopathic Pulmonary Fibrosis
Description:
Questionnaire evaluation
Sarciodosis
Description:
Questionnaire evaluation
Healthy Controls
Description:
Questionnaire evaluation

Trial contacts and locations

1

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Central trial contact

Christopher Atkins, MBBS, MRCP; Andrew M Wilson, MRCP, MD

Data sourced from clinicaltrials.gov

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