Status:

COMPLETED

Digital Tool Enhancing GPs' Information Management for Patients with Multimorbidity - a Pilot Study

Lead Sponsor:

Universitätsklinikum Hamburg-Eppendorf

Conditions:

Asthma

Breast Neoplasms

Eligibility:

All Genders

65+ years

Phase:

NA

Brief Summary

The gp-multitool.de study is a cluster-randomized controlled trial that aims to enhance evidence-based and patient-centered care for patients with multimorbidity by assessing and providing information...

Detailed Description

The gp-multitool.de study is a cluster-randomized controlled trial that enhances evidence-based and patient-centered care for patients with multimorbidity by assessing and providing information releva...

Eligibility Criteria

Inclusion

  • participation in a DMP; in Germany, DMPs have been implemented in outpatient care for asthma, breast neoplasms, coronary heart disease, diabetes mellitus type 1, diabetes mellitus type 2, and chronic obstructive pulmonary disease
  • at least two of the following coexisting conditions: Hypertension, Lipid metabolism disorders, Chronic low back pain, Severe vision reduction, Joint arthrosis, Diabetes mellitus, Chronic ischemic heart disease, Thyroid dysfunction, Cardiac arrhythmias, Obesity, Hyperuricemia/Gout, Prostatic hyperplasia, Lower limb varicosis, Liver diseases, Depression, Asthma/COPD, Gynaecological problems, Atherosclerosis/PAOD, Osteoporosis, Renal insufficiency, Cerebral ischemia/Chronic stroke, Cardiac insufficiency, Severe hearing loss, Chronic cholecystitis/Gallstones, Somatoform disorders, Hemorrhoids, Intestinal diverticulosis, Rheumatoid arthritis/Chronic polyarthritis, Cardiac valve disorders, Neuropathies, Dizziness, Dementias, Urinary incontinence, Urinary tract calculi, Anemias, Anxiety, Psoriasis, Migraine/chronic headache, Parkinson's disease, Cancers, Allergies, Chronic gastritis/GERD, Sexual dysfunction, Insomnia, Tobacco abuse, Hypotension

Exclusion

  • no capacity to consent
  • functional limitations precluding participation in the intervention (eg, loss of vision)
  • functional limitations precluding participation in telephone interviews (eg, loss of hearing)
  • limited German language skills precluding participation in telephone interviews
  • no access to a personal device with access to the internet (i.e., smartphone, tablet or personal computer)
  • participation in other trials during the observation time of the pilot study

Key Trial Info

Start Date :

October 2 2023

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 29 2024

Estimated Enrollment :

123 Patients enrolled

Trial Details

Trial ID

NCT06061172

Start Date

October 2 2023

End Date

August 29 2024

Last Update

December 12 2024

Active Locations (1)

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Universitätsklinikum Hamburg-Eppendorf

Hamburg, Germany, 20246