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Clinical Trials/NCT02257190
NCT02257190CompletedNot Applicable

The Features Behind the Beneficial Effects of Interval-walking

Rigshospitalet, Denmark2 sites in 1 country12 target enrollmentStarted: October 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
12
Locations
2
Primary Endpoint
Glycemic control

Study Overview

Brief Summary

A single bout of Interval-Walking (IW) exercise is superior to energy-expenditure and time-duration matched Continuous Walking (CW) exercise upon improving glycemic control. The reason IW is superior is unknown.

This study will look into whether it is the larger peak intensity during IW or if it is the alternating exercise pattern that is responsible for the larger improvements seen.

Subjects with type 2 diabetes will be included in a crossover, counter-balanced, controlled study, where each subject will undergo three trials. Trials will be identical except the following interventions:

  1. One hour of rest (Con)
  2. One hour of classical interval walking (repeated cycles of 3 min of fast and 3 min of slow walking; IW3)
  3. One hour of fast alternating interval walking (repeated cycles of 1 min of fast and 1 min of slow walking; IW1).

After the interventions subjects will undergo a standardized mixed meal tolerance test, with consecutive measurements of blood glucose, insulin and c-peptide.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
30 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Type 2 diabetes mellitus
  • Body mass index > 18 but < 40 m2/kg
  • Agreement to pause antidiabetic medication from 2 days before to after each trial

Exclusion Criteria

  • Pregnancy
  • Use of exogenous insulin
  • Contraindication to increased levels of physical activity
  • Evidence of thyroid, liver, lung, heart or kidney disease

Outcomes

Primary Outcomes

Glycemic control

Time Frame: Within the first 4 hours after the interventions

Glycemic control will be measured after each intervention. Subjects will receive a standardized mixed meal tolerance test (MMTT), and blood glucose values will be obtained during the test.

Secondary Outcomes

  • Insulin secretion(Within the first 4 hours after the interventions)
  • Insulin sensitivity(Within the first 4 hours after the interventions)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Anders Rasmussen Rinnov

MD, PhD

Rigshospitalet, Denmark

Study Sites (2)

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