Biweekly Interval Intermittent Fasting for Type 2 Diabetes, a Safety Study

Status Terminated

Clinical Trial Summary

The purpose of this study is to establish safety of biweekly intermittent fasting in the setting of type 2 diabetes mellitus or prediabetes under treatment with non-hypoglycemic agents (e.g. metformin).

Clinical Trial Description

This study is proposed as a prospective interventional cohort safety study for biweekly intermittent fasting. In the effort to improve compliance of lifetime dietary change, the version of 5:2 intermittent fasting to be applied in this study will be somewhat less intensive than implemented then what has been proposed in some recent, similar studies. On fasting days, instead of limiting the subject to a specific calorie count, the subject will be instead instructed to skip either the first or last meal of the day in order to complete a 12 to 16 hour fast, during which time they are allowed drink water or any non-caloric beverage of their choice, but not consume any calories. Furthermore, the patient will be instructed for their remaining 2 meals to consume no more than they would on a normal, non-fasting day. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03938441
Study type	Interventional
Source	Mike O'Callaghan Military Hospital
Contact
Status	Terminated
Phase	N/A
Start date	July 31, 2019
Completion date	May 28, 2021

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