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The Effect of Blood Volume Changes on the Glucose Tolerance (BV-GT)

Primary Purpose

Healthy, Overweight

Status
Unknown status
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Bedrest
Exercise Training
Sponsored by
Carsten Lundby
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Healthy focused on measuring before and after bedrest, healthy untrained, before and after exercise training

Eligibility Criteria

18 Years - 50 Years (Adult)MaleAccepts Healthy Volunteers

Bedrest:

Inclusion Criteria:

  • Informed consent as documented by signature
  • Age: 18-35
  • healthy (no chronic diseases)
  • BMI: 19-25
  • maximal oxygen uptake: 35-50 ml O2/min/kg

Exclusion Criteria:

  • chronic diseases
  • any health problems that do not allow the subjects to participate in the measurements (i.e. heart defect)
  • History of familiar history (1st grade relatives) of venous thrombic-embolism or renal insufficiency
  • Blood donation in the last month
  • Any medication with known influence on blood volume, glucose metabolism and body weight
  • Stay above 2500 m for more than 1 day
  • Known allergies against Fragmin or Heparin

Training:

Inclusion criteria:

  • Informed consent as documented by signature
  • Age: 35-50
  • BMI: 30-40
  • Fat%: 30-40 %
  • maximal oxygen uptake: 20-35 ml O2/min/kg
  • HbA1c: 5.5 - 7.0 %

Exclusion criteria:

  • Chronic diseases
  • Any health problems that do not allow the subjects to participate in the measurements (i.e. heart defect)
  • Blood donation in the last month
  • Any medication with known influence on blood volume, glucose metabolism and body weight
  • Stay above 2500 m for more than 1 day

Sites / Locations

  • Institute of Physiology, University of ZurichRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Bedrest

Exercise Training

Arm Description

4 days of bedrest

6 weeks of aerobic endurance exercise training with 4 supervised sessions per week at an average intensity of 65 % of maximal heart rate

Outcomes

Primary Outcome Measures

Change in blood volume
Change in glucose tolerance
Change in blood volume
Change in glucose tolerance

Secondary Outcome Measures

Full Information

First Posted
November 13, 2015
Last Updated
November 19, 2015
Sponsor
Carsten Lundby
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1. Study Identification

Unique Protocol Identification Number
NCT02612597
Brief Title
The Effect of Blood Volume Changes on the Glucose Tolerance
Acronym
BV-GT
Official Title
The Effect of Blood Volume Changes After Bed Rest and Aerobic Exercise Training on the Glucose Tolerance
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Unknown status
Study Start Date
January 2015 (undefined)
Primary Completion Date
April 2016 (Anticipated)
Study Completion Date
April 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Carsten Lundby

4. Oversight

5. Study Description

Brief Summary
In this study the investigators would like to elaborate on the mechanisms that lead to a higher insulin sensitivity after exercise training and a lower insulin sensitivity after bedrest. The investigators speculate that the concomitant chances in blood volume during training and bedrest might explain the changed insulin sensitivity because with a changing blood volume also the dilution space of the glucose will change. Furthermore, the investigators would like to work on the influence of a changed capacity of skeletal muscle for glucose uptake and glycogen storage on the glucose sensitivity. Therefore, A) a bed rest study with healthy untrained subjects and B) a training study with obese pre-diabetic patients will be conducted.
Detailed Description
While there is little doubt that physical inactivity leads to reduced insulin sensitivity and in contrast hereto that physical activity improves insulin sensitivity the underlying mechanisms are still to a large extend unknown. With this study the investigators wish to test two independent hypotheses that may explain the observed changes: The first hypothesis is that part of the explanation for the known increase in circulating levels of glucose in response to an oral glucose tolerance test (indicating reduced insulin sensitivity) following bed rest is due to a concomitantly reduced blood volume and thereby dilution space. In addition the investigators also speculate that the reduced glucose response to an oral glucose tolerance test (indicating improved insulin sensitivity) after a training period is related to the exercise induced increase in blood volume, and hence an increased dilution space. Based on this, the hypothesis to be tested with these two experimental approaches (bed rest and aerobic exercise training), is that at least part of the changes observed in the glucose tolerance following bed rest and aerobic exercise training are related to concomitantly occurring changes in blood volume. The second hypothesis to be tested is that another important contributor to the changes in circulating glucose levels following an oral glucose tolerance test after bed rest and physical training are related to diminished or improved capacity for skeletal muscle glucose uptake and glycogen storage, respectively. The rationale here fore are that exercise training increases skeletal muscle glycogen content and storage capacity in healthy and type 2 diabetic patients, respectively, and that bed rest does the opposite. To test this hypothesis two different intervention studies will be conducted. Study 1 is a bed rest study with healthy untrained subjects and study 2 is a training study with obese "pre-diabetic patients".

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy, Overweight
Keywords
before and after bedrest, healthy untrained, before and after exercise training

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Bedrest
Arm Type
Experimental
Arm Description
4 days of bedrest
Arm Title
Exercise Training
Arm Type
Experimental
Arm Description
6 weeks of aerobic endurance exercise training with 4 supervised sessions per week at an average intensity of 65 % of maximal heart rate
Intervention Type
Other
Intervention Name(s)
Bedrest
Intervention Type
Other
Intervention Name(s)
Exercise Training
Primary Outcome Measure Information:
Title
Change in blood volume
Time Frame
Baseline and 4 days
Title
Change in glucose tolerance
Time Frame
Baseline and 4 days
Title
Change in blood volume
Time Frame
Baseline and 6 weeks
Title
Change in glucose tolerance
Time Frame
Baseline and 6 weeks

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Bedrest: Inclusion Criteria: Informed consent as documented by signature Age: 18-35 healthy (no chronic diseases) BMI: 19-25 maximal oxygen uptake: 35-50 ml O2/min/kg Exclusion Criteria: chronic diseases any health problems that do not allow the subjects to participate in the measurements (i.e. heart defect) History of familiar history (1st grade relatives) of venous thrombic-embolism or renal insufficiency Blood donation in the last month Any medication with known influence on blood volume, glucose metabolism and body weight Stay above 2500 m for more than 1 day Known allergies against Fragmin or Heparin Training: Inclusion criteria: Informed consent as documented by signature Age: 35-50 BMI: 30-40 Fat%: 30-40 % maximal oxygen uptake: 20-35 ml O2/min/kg HbA1c: 5.5 - 7.0 % Exclusion criteria: Chronic diseases Any health problems that do not allow the subjects to participate in the measurements (i.e. heart defect) Blood donation in the last month Any medication with known influence on blood volume, glucose metabolism and body weight Stay above 2500 m for more than 1 day
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carsten Lundby, Prof. Dr.
Phone
+41 44 635 50 52
Ext
+41
Email
carsten.lundby@access.uzh.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carsten Lundby, Prof. Dr.
Organizational Affiliation
Institute of Physiology, University of Zurich
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Physiology, University of Zurich
City
Zurich
ZIP/Postal Code
8057
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carsten Lundby, Prof. Dr.
Phone
+41 44 635 50 52
Ext
+41
Email
carsten.lundby@access.uzh.ch

12. IPD Sharing Statement

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The Effect of Blood Volume Changes on the Glucose Tolerance

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