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The Effect of Blood Volume Changes on the Glucose Tolerance

The Effect of Blood Volume Changes After Bed Rest and Aerobic Exercise Training on the Glucose Tolerance

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02612597
Acronym
BV-GT
Enrollment
20
Registered
2015-11-24
Start date
2015-01-31
Completion date
2016-04-30
Last updated
2015-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy, Overweight

Keywords

before and after bedrest, healthy untrained, before and after exercise training

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.

Interventions

OTHERBedrest
OTHERExercise Training

Sponsors

Carsten Lundby
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion 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 %

Design outcomes

Primary

MeasureTime frame
Change in blood volumeBaseline and 4 days
Change in glucose toleranceBaseline and 4 days

Countries

Switzerland

Contacts

Primary ContactCarsten Lundby, Prof. Dr.
carsten.lundby@access.uzh.ch+41 44 635 50 52

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026