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Chronic Obstructive Pulmonary DiseaseAMICENCT01293890

Adherence to Medication and Its Impact on Chronic Obstructive Pulmonary Disease (COPD) Exacerbations: The AMICE Prospective Study

An observational study of Chronic Obstructive Pulmonary Disease, run by KU Leuven at 1 site in Belgium.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Chronic Obstructive Pulmonary Disease (COPD) represents one of the most challenging chronic diseases of the 21st century: it is expected to be the fourth leading cause of death by 2030. Read more about this study

Who is it for?
Ages 40 years and older
Conditions the study is for
Chronic Obstructive Pulmonary Disease
How many people
100 participants
Where
1 siteBelgium
Study dates
Mar 2011to Sep 2014
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: patients that are admitted to the Pneumology of Geriatry Service of UZ Leuven after entering the emercency ward with a COPD exacerbation

Who may be able to join

  • Clinical diagnosis of COPD
  • Age > 40 years old
  • Documented spirometry within the last 12 months with a post-bronchodilator FEV1 < 80% of predicted and an FEV1 < 70% of FVC (4 puffs of salbutamol 30 minutes prior to spirometry)
  • Patients being hospitalized for an exacerbation at the University Hospitals of Leuven at time of enrollment
  • Patients currently treated with Spiriva for at least 4 weeks at the start of the data collection (i.e. 4 weeks after hospitalization for an exacerbation)
  • Oral fluency in Dutch
  • Being capable to provide informed consent

Who cannot join

  • A documented history of asthma or another respiratory disease
  • An expected life expectancy of < 6 months
  • Cognitive impairment (Mini Mental State Examination test results < 25) or presence of other co-morbidities preventing patients from completing the self-report instruments and/or using electronic monitoring
  • Institutionalized patients, patients living in a nursing home or patients not managing their medications independently

Trial locations and contacts

1 site in 1 country.

Marc Decramer, MD, PhD contact

3216346800

marc.decramer@uz.kuleuven.be

Janssens Wim, MD, PhD contact

016/340 957

wim.janssens@uz.kuleuven.be

Belgium1 site, 1 recruiting
  • University Hospital Leuven

    Leuven, Flanders, 3000

    Marc Decramer, MD, PhD

    Wim Janssens, MD, PhD

    Recruiting

Other trials in Belgium

About this study

Official title: Adherence to Medication and Its Impact on COPD Exacerbations: The AMICE Prospective Study

Chronic Obstructive Pulmonary Disease (COPD) represents one of the most challenging chronic diseases of the 21st century: it is expected to be the fourth leading cause of death by 2030. COPD is characterized by pulmonary and extra-pulmonary systemic manifestations caused by partly irreversible expiratory airflow obstruction. The cornerstone of COPD management is the prescription of single or combined inhalation therapy, such as short- and long-acting bronchodilators, inhaled corticosteroids to possibly prevent disease progression, preserve lung function, relieve respiratory symptoms and prevent or treat exacerbations. Given the complex and lifelong treatment, one can expect that adherence to the prescribed inhalation therapy is not self-evident. Adherence can be defined as the "the extent to which a person's behaviour (taking medications, following a recommended diet and/or executing life-style changes) corresponds with the agreed recommendations of a health care provider". Inhaled medications have an additional complexity in that patients who intend to be adherent may be take the inhaled medication incorrectly, prohibiting proper therapeutic action. Taking less than the prescribed amount of medication, missing doses or stopping treatment for brief or extended periods will put the patient at risk for suboptimal disease control. Hence, the effectiveness will largely depend on the patient's ability to manage their disease adequately in daily life.

Using electronic monitoring, 3 studies in COPD found a prevalence of medication non-adherence of 51% which was worse than the average prevalence of 29% (range 3-66%) found across diseases such as hypertension, cancer, epilepsia, infections and HIV.

Read more

The existing evidence on risk factors for nonadherence in COPD is mostly anecdotic and not guided by behavioral models. According to the integrated model of behavioral prediction (IMBP), barriers, skills and ability and intention are the most important drivers of adherence (i.e. medication adherence).

The aims of the study are the following:

  • To prospectively investigate the impact of medication nonadherence on time to exacerbation (primary end-point) and exacerbation rate, FEV1, hospitalization rate and duration, and quality of life (secondary end-points) at 1 year follow-up using electronic monitoring
  • To investigate risk factors for medication nonadherence, using the Integrated Model of Behavioral Prediction as a theoretical framework
  • To determine the diagnostic accuracy of different measures of medication nonadherence (i.e. pill count, self-report and physician rating) relative to electronic monitoring.
  • To investigate the prevalence of nonadherence to other aspects of the therapeutic regimen, i.e. the use of concomitant medications, smoking cessation, alcohol use, physical activity, attendance to rehabilitation sessions and dietary adherence, their interrelations, and impact (alone and in combination) on time to first exacerbation.
  • To investigate the interrelations in adherence to the various components of the therapeutic regimen.
  • To investigate the impact of nonadherence to the other components of the therapeutic regimen (alone and in combination) on clinical outcomes (i.e. time to exacerbation, exacerbation rate/PPY, FEV1, hospitalization rate and duration, and quality of life at 1 year follow-up.
Keywords
adherence, medication, exacerbations, hospital admission
Medical subject headings
Pulmonary Disease, Chronic Obstructive

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01293890
Study groupRoleWhat they receive
COPD patients with hospital admission for exacerbationNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. time to exacerbation

    Measured: 1 year

Secondary outcomes (5)
  1. exacerbation rate

    Measured: 1 year

  2. Forced expiratory volume in one second (FEV1)

    Measured: 1 year

  3. Number of hospitalization rate due to exacerbations

    Measured: 1 year

  4. Duration of hospitalizations due to exacerbations

    Measured: 1 year

  5. Functional status

    Measured: 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Feb 2011 (estimated)
  2. Study startMar 2011
  3. Primary completionSep 2014 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01293890
Sponsor's protocol ID
B322201110500
Acronym
AMICE
Status last verified
Jul 2013
First submitted
10 Feb 2011
Last updated
30 Jul 2013
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Chronic Obstructive Pulmonary Disease, run by KU Leuven at 1 site in Belgium.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 30 Jul 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Marc Decramer, MD, PhD (3216346800, marc.decramer@uz.kuleuven.be), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

time to exacerbation (time frame: 1 year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Jul 2013.

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