Selfcare MAnagement InteRvenTion in COPD (SMART COPD)

  • STATUS
    Recruiting
  • participants needed
    60
  • sponsor
    Lund University
Updated on 5 August 2020
dyspnea

Summary

To evaluate whether a digital support and communication platform for COPD patients after 6 months provides:

  1. Decreased breathlessness on the basis of modified medical research council dyspnea scale [mMRC]
  2. Improved health status and symptom relief based on COPD assessment scale [CAT]
  3. Improved quality of life based on EQ-5D
  4. Reduction in the number of incidents, hospital nights, the number of hospitalizations, outpatient contacts or the number of deaths related to COPD
  5. A change in the classification of COPD severity based on GOLD A-D

Details
Condition Self-Assessment, Chronic Obstructive Lung Disease, Chronic Obstructive Lung Disease, Hospitalization
Age 100years or below
Treatment LifePod
Clinical Study IdentifierNCT04416295
SponsorLund University
Last Modified on5 August 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

The patient is included in the study in connection with visits to COPD
Diagnosed COPD J44 (newly discovered or existing)
Have completed the consent form
Is judged to be able to handle the intervention himself or with the help of staff or relatives

Exclusion Criteria

Patient who declines to participate in the trial
Impaired cognitive ability that is judged to affect the ability to conduct the study in the intended manner
Life expectancy <8 months
In other ways, treating physicians are deemed to be inappropriate to participate in the study, e.g. due to participation in another study
Clear my responses

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.