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CompletedNCT01325948COPD LIFEUpdated Jul 21, 2011

Cross-sectional Study to Investigate the Effects of Chronic Obstructive Pulmonary Disease on Daily Life Activities

An observational study in Chronic Obstructive Pulmonary Disease, sponsored by AstraZeneca. Completed at 20 sites in Turkey. Open to participants aged 45 Years and older. Per ClinicalTrials.gov, last updated 2011-07-21.

Sponsored by AstraZeneca · Observational

Study type
Observational
Time perspective
Cross-sectional
Enrollment
497
Ages
45 Years and older
Sex
All
01

Study summary

The purpose of this study is to investigate the effects of Chronic Obstructive Pulmonary Disease (COPD) on daily life activities in patients with COPD and also to determine the socio-demographic profile, daily life style and needs of the patients with COPD.

02

Conditions studied

  • Chronic Obstructive Pulmonary Disease

Keywords

  • COPD
03

In context

Lung Diseases

3,303 studies on the registry are indexed under Lung Diseases; 355 are open to participants now.

This study's enrollment of 497 is above the median of 157 across 929 observational studies indexed under Lung Diseases.

Browse Lung Diseases studies →

Lead sponsor

AstraZeneca is the lead sponsor of 3,429 studies on the registry; 270 are open to participants now.

Of its 357 completed or terminated interventional studies of FDA-regulated products, 173 (48%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Outpatients from health institutions where the patients with COPD are treated

Inclusion criteria

  • Diagnosis of COPD
  • Outpatient treatment for any reason
  • Current or ex-smoker

Exclusion criteria

Exclusion Criteria:

  • An exacerbation of COPD that still lasts or that was experienced within last 3 months
  • History of asthma and/or allergic rhinitis
  • The presence of another important respiratory disease
05

Study design

Time perspective
Cross-sectional
Enrollment
497 participants (actual)

Groups and cohorts

  • Patients with COPD
06

What researchers measure

Primary outcomes

  1. Effect of COPD on daily activities

    The distribution of the patients according to their answers, as Yes / No / Unknown, given to the questions of patient questionnaire about the effect of COPD on daily life and which daily activities are limited will be calculated as percentage.

    Time frame: 1 year

Secondary outcomes

  1. Patients' socio-demographic profiles, daily life conditions and needs and expectations from therapy

    The answers the patients give to the questions about socio-demographic profiles, daily life conditions and needs and their expectations from the therapy will be summarized as percentages: Age and gender, educational background, place of residence, marital status and life conditions, concomitant diseases, smoking status, the diagnosis of COPD and its clinical characteristics basic knowledge of the patient about COPD daily life of the patient, expectations from the therapy.

    Time frame: Baseline

07

Study locations

20 sites
  • Research Site
    Adana, Turkey
  • Research Site
    Ankara, Turkey
  • Research Site
    Antalya, Turkey
  • Research Site
    Aydin, Turkey
  • Research Site
    Bartin, Turkey
  • Research Site
    Bolu, Turkey
  • Research Site
    Burdur, Turkey
  • Research Site
    Bursa, Turkey
  • Research Site
    Gaziantep, Turkey
  • Research Site
    Gebze, Turkey
  • Research Site
    Giresun, Turkey
  • Research Site
    Isparta, Turkey
  • Research Site
    Istanbul, Turkey
  • Research Site
    Izmir, Turkey
  • Research Site
    Karabuk, Turkey
  • Research Site
    Kayseri, Turkey
  • Research Site
    Konya, Turkey
  • Research Site
    Manisa, Turkey
  • Research Site
    Mersin, Turkey
  • Research Site
    Yozgat, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 21, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01325948
Lead sponsor
AstraZeneca
First posted
Mar 30, 2011
Start date
Mar 2011
Primary completion
Jun 2011
Completion
Jun 2011
Last update
Jul 21, 2011

Study contacts

Zeynep Goztas
study director · AstraZeneca Turkey
Mehmet Polatli
principal investigator · Adnan Menderes University Faculty of Medicine

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2011. You cannot join it, but the record below documents what was studied.

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