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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02251301
Other study ID # H14-01636
Secondary ID
Status Completed
Phase N/A
First received September 25, 2014
Last updated May 1, 2017
Start date January 2015
Est. completion date January 2017

Study information

Verified date August 2016
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate whether combining interval training with skim milk supplementation will result in improved glucose control and markers of cardiovascular health in people with type 2 diabetes. Participants will complete supervised interval training three times a week over a 12 week training period while consuming skim-milk, whey/casein protein drink, or a placebo beverage that does not contain any calories or vitamins/minerals immediately and 1 hour after each training session. After twelve weeks participants will repeat baseline tests to examine any effects of the intervention on their glucose control, fitness, blood vessel function, body composition, and blood markers of inflammation.


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date January 2017
Est. primary completion date January 2017
Accepts healthy volunteers No
Gender All
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria:

- Aged between 40 and 75.

- Diagnosed with type 2 diabetes for more than 6 months.

- On stable medication for the last 6 months

Exclusion Criteria:

- Type 2 diabetes controlled with exogenous insulin

- Uncontrolled hypertension (blood pressure >160/90 mmHg)

- History of heart disease, myocardial infarction or stroke

- Any other contraindications to exercise

Study Design


Intervention

Dietary Supplement:
Skim Milk
250 ml skim milk will be consumed by participants immediately and 1 hour after each of the 36 sessions of high-intensity interval training over a 12 week period.
Behavioral:
High intensity interval training
All participants will undergo a 12 week high intensity interval training program consisting of 3 supervised sessions a week of 4-10 x 1 min high intensity interval alternating with 1 min of recovery.
Other:
Placebo
250 mL water will be consumed by participants immediately and 1 hour after each of the 36 sessions of high-intensity interval training over a 12 week period.
Dietary Supplement:
Macronutrient isoenergetic control
250 mL of protein+cho matched drink will be consumed by participants immediately and 1 hour after each of the 36 sessions of high-intensity interval training over a 12 week period.

Locations

Country Name City State
Canada University of British Columbia, Okanagan. Kelowna British Columbia

Sponsors (2)

Lead Sponsor Collaborator
University of British Columbia Dairy Farmers of Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Change from baseline in fasting plasma non esterified free fatty acid concentration at end of week 12 of intervention. Baseline, Week 12
Other Change from baseline in systolic blood pressure at end of week 12 of intervention. Baseline, Week 12
Other Change from baseline in diastolic blood pressure at end of week 12 of intervention. Baseline, Week 12.
Other Change from baseline in circulating inflammatory cytokines at end of week 12 of intervention. Baseline, Week 12.
Other Change from baseline in body composition as measured by dual absorbancy x ray at end of week 12 of intervention. Baseline, Week 12.
Other Change from baseline in task switching capabilities at end of week 12 of intervention. Baseline, Week 12.
Primary Change from baseline in glycemic control assessed by continuous glucose monitoring at end of week 12 of intervention Baseline, Week 12.
Secondary Change from baseline in hemoglobin A1C percentage at end of week 12 of intervention. Baseline, Week 12.
Secondary Change from baseline in fasting plasma glucose concentration at end of week 12 of intervention. Baseline, Week 12.
Secondary Change from baseline in fasting plasma insulin concentration at end of week 12 of intervention. Baseline, Week 12.
Secondary Change from baseline in flow mediated dilation of brachial artery at end of week 12 of intervention. Baseline, Week 12.
Secondary Change from baseline in peak oxygen uptake as a measure of aerobic fitness at end of week 12 of intervention. Baseline, Week 12
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