Clinical Trial Details
— Status: Active, not recruiting
Administrative data
NCT number |
NCT04458038 |
Other study ID # |
19/44919 |
Secondary ID |
|
Status |
Active, not recruiting |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
December 7, 2020 |
Est. completion date |
December 31, 2023 |
Study information
Verified date |
December 2023 |
Source |
Sygehus Lillebaelt |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Studies have documented impaired cognitive function in patients with COPD. The possible
reasons for this and correlation to the severity of the disease are not well described. This
explorative study examines the cognitive skills of COPD patients, quantified by their ability
to drive a vehicle and other cognitive test. Furthermore, we want to study the cognitive
skills in COPD patients before and after they are diagnosed with and treated for obstructive
sleep apnoea (OSA). The overall hypothesis is that chronic lung patients´ cognitive skills
correlate with the severity of their disease. We expect that their ability to drive a vehicle
drops in relation to the severity of the disease and to comorbidities.
Description:
200 COPD patients recruited from the outpatient clinic at the Department of Respiratory
Diseases at Vejle Hospital. Approximately 2600 COPD patients are treated in Vejle.
For this study a driving simulator is being used. The subjects are placed in front of a
computer monitor which simulates a horizon on the middle of the screen, and a road that
appears in the bottom half of the screen. The subjects are encouraged to keep the virtual
vehicle on the road, using a steering wheel in front of them. Simultaneous, they are required
to keep focus on both sides of the screen where a line of numbers is frequently changing.
Every time the number 2 occurs, the subjects must press a button on the steering wheel.
The subjects´ overall ability to control the driving simulator is being expressed by the
standard deviation (sd) of distance of the car´s centre to the centre of the road and the
number of off-road events. Relevant cognitive measurements, such as reaction speed and
ability to split attention, are quantified by the reaction speed to the occurrence of the
number 2. The reason for this is that the software of the simulator measures the mean
reaction time from the number have occurred until the correct button is pressed, and the
number of nil-responses, where the number 2 is not detected.
Every participating subject will receive a 5 minutes testing period of the simulator followed
by 30 minutes of applicable driving time.The other tests will be performed/collected just
after the driving test.
Besides the driving simulator and tests (see sections below) following are obtained: 1) Lung
function (FEV1, FVC and FEV1/FVC), 2) Arterial blood sample including PaO2, PaCO2 and
carbonmonooxidhemoglobin (HbCO) (1.5 ml), 3) Smoking status and number of pack years, 4)
Status of oxygen therapy, 5) Number of COPD exacerbations in the last year, 6) Comorbidities
such as diabetes, metabolic diseases, cardiovascular diseases, kidney insufficiency, 7)
Medicine, 8) Height and weight, 9) Level of education, 10) Degree of dyspnoea Medical
research Council breathlessness scale (MRC-scale) and 11) Global initiative for chronic
Obstructive Lung Disease (GOLD) classification of airflow limitation.
The blood samples will be analysed immediately after they are taken, and as a consequence no
biobank will be established. The information will be gathered from the journals and from
patient interview in connection with the trial. The information will be used in the
assessment of possible reasons to COPD patients´ expected reduced cognitive skills.
The NOX T3TM (see section below) will be delivered in connection with the trial. If the
patients are diagnosed with OSA they will shortly after receive standard treatment in the
public Sleep Clinic at Vejle Hospital, if the patients accept. After 2-3 month of treatment,
the patients will repeat all the tests and blood samples, except the cardiorespiratory
monitoring.
To exclude that an improvement of skills is not due to the patients having learned how to
improve the test, we will establish a control group. The control group must consist of COPD
patients without OSA who must perform a retest like the patients with OSA.