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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04520763
Other study ID # HOGTT_2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 20, 2020
Est. completion date April 21, 2022

Study information

Verified date March 2023
Source Swiss Federal Institute of Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the acute effects of respiratory muscle exercises vs. a control intervention on blood glucose kinetics in healthy adults after an oral glucose tolerance test.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date April 21, 2022
Est. primary completion date April 21, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age =18 years - Healthy - Non-smoking - Body mass index (BMI): 18.5 - 29.9 kg·m-2 - Normal lung function - Willing to adhere to study rules Exclusion Criteria: - Known or suspected non-compliance, drug or alcohol abuse - Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant - Previous enrolment into the current study - Intake of medications affecting metabolism, the cardiovascular or the respiratory system, or sleep - Acute illness or chronic conditions of the gastrointestinal tract, and health conditions affecting metabolism, the cardiovascular or the respiratory system, or sleep - Pregnancy, breastfeeding, or intention to become pregnant during the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
5min respiratory muscle exercises
5 min of hyperpnea at a target intensity of 60-80% MVV 15-30min after ingestion of 75g of glucose
15min respiratory muscle exercises
5 min of hyperpnea at a target intensity of 60-70% MVV 15-30min after ingestion of 75g of glucose

Locations

Country Name City State
Switzerland Exercise Physiology Lab, Institute of Human Movement Sciences and Sport, ETH Zurich Zürich ZH

Sponsors (1)

Lead Sponsor Collaborator
Swiss Federal Institute of Technology

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Peak blood glucose concentration Peak blood glucose concentration will be determined in the three conditions (5min or 15min respiratory muscle exercises or control). throughout the study, an expected average of 2 weeks per participant
Primary area under the glucose-time curve Area under the glucose-time curve will be determined in the three conditions (5min or 15min respiratory muscle exercises or control). throughout the study, an expected average of 2 weeks per participant
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