A Parallel Group Randomized Trial Investigating the Effect of Hepatic Fat Depletion Via a Very-low Calorie Diet on Hepatokine Secretion and Function in People With Type 2 Diabetes

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The aim of this randomized trial is to determine whether liver fat depletion via a short-term (i.e., two weeks) very-low calorie diet will restore the normal exercise-induced secretion of a signaling protein (fibroblast growth factor 21) from the liver in people living with type 2 diabetes. Participants will have their liver fat, body composition, and various markers of metabolic health assessed and then will be randomized to either the very-low calorie diet intervention or a free-living control group for two weeks. Upon completion of the two-week intervention period, participants will redo all of the pre-intervention assessments. The changes in the assessments from before vs. after the intervention period will be compared between the two intervention groups (i.e., the very-low calorie diet group vs. the free living control group).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 30
Maximum Age: 70
Healthy Volunteers: f
View:

• Men and women 30-70 years of age

• The target population is persons with type 2 diabetes. I.e., persons are eligible if they are diagnosed with type 2 diabetes either only with metformin for managing glucose or without use of glucose lowering medications. Persons with a HbA1c ≥ 48 mmol/mol with or without the use of glucose lowering medications are also eligible. Any glucose lowering medications other than metformin are disallowed (described under Exclusion criteria, below)

• Diabetes duration \< 7 years

• Body Mass Index (BMI) ≥ 30 kg/m2 and ≤ 40 kg/m2

• Accepts medical regulation by the study endocrinologist

• Inactivity, defined as \< 1,5 hours of structured physical activity pr. week at moderate intensity and cycling \< 30 minutes/5 km pr. day at moderate intensity (moderate intensity = out of breath but able to speak)

Locations
Other Locations
Denmark
Rigshospitalet - CFAS
RECRUITING
Copenhagen
Contact Information
Primary
Cody G Durrer, Ph.D.
cody.garett.durrer@regionh.dk
+4550104538
Time Frame
Start Date: 2024-02-01
Estimated Completion Date: 2026-03
Participants
Target number of participants: 42
Treatments
Experimental: Very-low calorie diet
Two weeks of \~800kcal/day
No_intervention: Free-living control
No intervention control group
Related Therapeutic Areas
Sponsors
Collaborators: Canadian Institutes of Health Research (CIHR), Diabetesforeningen, Region Hovedstadens Forskningsfond
Leads: Rigshospitalet, Denmark

This content was sourced from clinicaltrials.gov