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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02196623
Other study ID # HA 7037/2-1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2015
Est. completion date January 2019

Study information

Verified date August 2017
Source Hannover Medical School
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Ageing is the primary risk factor for most chronic diseases including type 2 diabetes mellitus. Sarcopenia and muscular mitochondrial dysfunction with aging are crucial mechanisms leading to decreased exercise tolerance and worsened insulin sensitivity. Thus, metabolic disease and frailty, which limits physical mobility as well as quality of life, share common cellular mechanisms.

The investigators will test the hypothesis that a combination of normobaric hypoxia and exercise training elicits a synergistic effect on age-associated metabolic skeletal muscle dysfunction and the investigators will address the molecular mechanisms. In a randomized clinical study, the investigators will compare normoxic and hypoxic training conditions in elderly subjects. Outcome measures will focus on whole body insulin sensitivity and mitochondrial responses in skeletal muscle before and after the 8-week training intervention.


Recruitment information / eligibility

Status Completed
Enrollment 29
Est. completion date January 2019
Est. primary completion date September 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 55 Years to 75 Years
Eligibility Inclusion Criteria:

- 55 to 75 years of age

- body mass index: 20 - 35 kg/m2

- weight stable during last 6 months before screening (weight change < 2% body weight)

- HOMA-index of insulin resistance = 2 to 4 units

Exclusion Criteria:

- more than 1 hour of scheduled exercise training per week

- known diagnosis of type 2 diabetes or measured HbA1c > 6,5%

- known drug or alcohol abuse

- any contraindication to perform exercise training

- acute or chronic infections

- increased bleeding risk by history, INR > 1,3, use of anticoagulants

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Hypoxic exercise
Supervised, progressive aerobic exercise program for 8 weeks under hypoxic conditions
Normoxic Exercise
Supervised, progressive aerobic exercise program for 8 weeks under normoxic conditions

Locations

Country Name City State
Germany Hannover Medical School Hannover Lower Saxony

Sponsors (2)

Lead Sponsor Collaborator
Hannover Medical School German Diabetes Center

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Insulin sensitivity Insulin sensitivity is assessed via the hyperinsulinemic euglycemic glucose clamp and expressed as the glucose infusion rate (GIR) in ml At baseline and after 8 weeks
Secondary Maximum oxygen uptake Maximum oxygen uptake is measured during an incremental exhaustive exercise test and is expressed in ml/min/kg At baseline and after 8 weeks
Secondary Mitochondrial number Mitochondrial number and selected gene expression assessed from muscle biopsies from the vastus lateralis. At baseline and after 8 weeks
Secondary Fat and carbohydrate oxidation during exercise Fat and carbohydrate oxidation during exercise is assessed during an incremental exercise test by measurements of gas exchange and expressed as g/min At baseline and after 8 weeks
Secondary Body fat and body fat free mass Measured via by air-displacement plethysmography (ADP) and expressed in kg At baseline and after 8 weeks
Secondary Health related quality of life Assessed using the short form 36 (SF-36) questionnaires At baseline and after 8 weeks
See also
  Status Clinical Trial Phase
Recruiting NCT04168424 - Validation of the English Version of the FIMA Questionnaire
Completed NCT02816580 - Biological MArkers of FRAilty in Elderly Subjects N/A