Study to Learn More About Outcomes Reported by Patients Suffering From Type 2 Diabetes Using a Digital Data Collection Tool

  • STATUS
    Recruiting
  • participants needed
    300
  • sponsor
    Bayer
Updated on 19 February 2024
metformin

Summary

In this study researchers want to gain more information on patients who are treated with Metformin for their Type 2 Diabetes. Adult female and male patients with a prescription of a Metformin containing drug will be invited to the study in a public pharmacy after the decision for treatment with Metformin has been made by the treating physician. The pharmacist will provide interested participants access to a special phone App and participants are asked to complete via this phone App a questionnaire on their health situation with special focus on their Type 2 Diabetes. This includes questions on complications and self-care activities in relation to their diabetes, questions on quality of life and health history. There will be no extra visit to the treating doctor or a pharmacy. The study is aiming to have the questionnaire completed by 300 participants.

Details
Condition NIDDM, diabetes mellitus, type 2, diabetes mellitus, type 2
Age 18-100 years
Treatment No intervention
Clinical Study IdentifierNCT04383041
SponsorBayer
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Adult female or male patient
Valid prescription for a Metformin containing drug approved in Germany
Decision to initiate treatment with Metformin was made by the treating physician as part of the routine treatment practice
Signed informed consent

Exclusion Criteria

Not applicable
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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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.

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

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