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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01823627
Other study ID # SJ-322
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2013
Est. completion date July 2013

Study information

Verified date May 2018
Source Psykiatrien Syd
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose: Patients with mental health disorders have a reduced life expectancy, compared to the general population. The shorter life expectancy is caused by natural and unnatural death. In general, patients with a mental disorder tend to have a more unhealthy lifestyle, than the general population, characterized by e.g. lack of exercise and smoking.

Hypothesis

Chronic obstructive pulmonary disease (COPD) is underdiagnosed in psychiatric inpatients There is a higher prevalence of COPD in psychiatric inpatients compared to the general population Screening of patients with one respiratory symptom and a smoking history, has the same sensitivity regarding to diagnosis of COPD, as screening all patients with a smoking history

Method:

80 psychiatric inpatients will undergo spirometry with reversibility test and COPD Assessment Test (CATest). Furthermore, patient history regarding respiratory symptoms and smoking will be taken into account.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date July 2013
Est. primary completion date June 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Inpatients in Psykiatrien Syd, Region Zealand, ward S1,S2,S3,S4,S5,S6

- Admission time over 48 hours

Exclusion Criteria:

- Patients who is not able to perform spirometry due to their psychiatric condition

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Spirometry with reversibility test
Spirometry with reversibility test and CATest questionaire. following will be measured FEV1 L/s FVC L/s FEV1/FVC ration

Locations

Country Name City State
Denmark Psyciatrien Syd, Region Zealand Vordingborg

Sponsors (2)

Lead Sponsor Collaborator
Psykiatrien Syd Naestved Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tiffeneau index - FEV1/FVC ratio at enrollment
Secondary forced vital capacity FVC L/s at enrollment
Secondary Forced expiratory volume in 1 second FEV1 L at enrollment
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