The goal of this observational study is to test if regular meetings (multidisciplinary team conferences) between several different medical doctors can work well in everyday hospital life. The doctor meetings are meant to discuss patients who have both diabetes and other chronic conditions at the same time. The main questions it aims to answer are: * How can the concept of these meetings work in everyday hospital life? * What are the patients and doctors getting out of the meetings? Patients with diabetes and concurrent other diseases will be asked: * if they want their case discussed on the doctor meeting * to answer a set of questions about their well-being and symptoms before and 6 months after the meeting * if the research group can store their information for the study Doctors participating in the meetings are asked to answer questions about what they have learned in the meetings.
Age range
18 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Recruitment
Timeframe: Full project period, 17 months.
Completion of PRO-questionnaire
Timeframe: Full project period, 17 months.
Technical difficulties i relation to MDT
Timeframe: Full project period, 17 months.
Time schedule
Timeframe: Full project period, 17 months.
MDT recommendations
Timeframe: Assessed at 6 month follow up.
Clinician preparation time
Timeframe: Full project period, 17 months.