Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Type 2 Diabetes
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Single (Outcomes Assessor)Masking Description: Participants and treatment providers will not be blinded to the allocated trial intervention. The treatment providers are not involved in the analyses. All other medical personnel will be blinded by blinding of notes in the participant's electronic records. Outcome assessors and external statisticians at the Copenhagen Trial Unit will be blinded to the randomisation status of the participants. The statistical analyses will be conducted with the intervention groups coded as X and Y. The steering committee will write two abstracts while the blinding is intact, one assuming the experimental intervention group is X and the control intervention group is Y, and one assuming the opposite. After this, the code will be broken.Primary Purpose: Supportive Care

Participation Requirements

Age
Between 18 years and 110 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04601311
Collaborators
  • Odense University Hospital
  • Copenhagen Trial Unit, Center for Clinical Intervention Research
  • Copenhagen University Hospital, Denmark
Investigators
Not Provided