DRKS00004346
Recruiting
N/A
Randomized controlled clinical pilot study for the implementation of medical group visits in Germany following the CHCC-Model (Cooperative Health Care Clinics) for the treatment of patients with diabetes type II or hyper tonus in family practice
Not provided0 sites384 target enrollmentOctober 4, 2012
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- I10
- Sponsor
- Not provided
- Enrollment
- 384
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •I.patients chronically suffering from
- •a.diabetes, defined as an HbA1C level larger than 8,5 % or
- •b.hyper tonus, defined as a level of mmHg larger than 140/90; it is sufficient if either the systolic or diastolic blood pressure value is exceeded,
- •II.patients older than 55 years (born in or before 1957\),
- •III.patients who visit their family physician most frequently, defined as 10 or more visits in connection with their chronic disease within the last 12 month,
- •IV.willingness to participate in medical group visits.
Exclusion Criteria
- •I.patients are terminally ill,
- •II.patients, who are unable to follow a discussion respectively who are unable to actively participate in medical group visits – be it out of cognitive impairment, dementia, deafness insufficient language skills or other reasons,
- •III.patients, who’s discretion in regards to the medical information’s of other patients are in question,
- •IV.patients, who are not interested in sharing their medical histories or issues in a group with other patients,
- •V.patients, who do not have transportation means to attend group visits on a regular basis,
- •VI.patients, who for other reasons are unable to attend group visits on a regular basis,
- •VII.patients, who are unable to participate in the study over the entire course of the study,
- •VIII.patients, who at the same time participate in a second clinical trial or who just completed a different clinical trial,
- •IX.patients, who did not consented to the participate by signing the consent form
Outcomes
Primary Outcomes
Not specified
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