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Clinical Trials/NCT02521025
NCT02521025CompletedNot Applicable

The Impact of Continuous Versus Intermittent Feeding on Changes in Insulin Sensitivity During Bed-rest

Maastricht University Medical Center1 site in 1 country20 target enrollmentStarted: October 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
20
Locations
1
Primary Endpoint
Change in insulin sensitivity (measured as glucose infusion rate during hyperinsulinaemic-euglycaemic clamp)

Study Overview

Brief Summary

In the present study, the investigators will assess the impact of two different feeding patterns (continuous vs intermittent) on insulin sensitivity and muscle mass following bedrest.

Detailed Description

In the present study, the investigators will assess the impact of two different feeding patterns on insulin sensitivity and muscle mass following bedrest. Healthy, young males will be fed in a continuous (no breaks in food supply) or intermittent (in boluses throughout the day) manner.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •BMI between 18.5 and 35
  • •Recreationally active

Exclusion Criteria

  • •Type 2 diabetes
  • •Performing progressive resistance training in 6 months prior to study
  • •Back/knee/leg problems
  • •Hypertension
  • •Use of certain anticoagulants
  • •All co morbidities interacting with mobility and muscle metabolism of the lower limbs
  • •Blood donation in past 3 months

Arms & Interventions

Intermittent feeding

Experimental

Intermittent feeding pattern throughout the bedrest period, with 4 boluses per day

Intervention: Intermittent feeding pattern (Other)

Continuous feeding

Experimental

Continuous feeding pattern throughout the bedrest period, with 4 boluses per day, without breaks in food supply.

Intervention: Continuous feeding pattern (Other)

Outcomes

Primary Outcomes

Change in insulin sensitivity (measured as glucose infusion rate during hyperinsulinaemic-euglycaemic clamp)

Time Frame: 7 days bedrest

Secondary Outcomes

  • Change in muscle mass (measured as upper leg muscle cross-sectional area with CT scan)(7 days bedrest)
  • Change in lean tissue (measured via DEXA scan)(7 days bedrest)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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