- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04520763
Effects of Respiratory Muscle Exercises on Glucose Tolerance in Healthy Adults
March 16, 2023 updated by: Swiss Federal Institute of Technology
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
42
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Christina M. Spengler, Prof.
- Phone Number: +41 44 635 5007
- Email: christina.spengler@hest.ethz.ch
Study Locations
-
-
ZH
-
Zürich, ZH, Switzerland, 8057
- Exercise Physiology Lab, Institute of Human Movement Sciences and Sport, ETH Zurich
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Respiratory Muscle Exercises
Two respiratory muscle exercises
|
5 min of hyperpnea at a target intensity of 60-80% MVV 15-30min after ingestion of 75g of glucose
5 min of hyperpnea at a target intensity of 60-70% MVV 15-30min after ingestion of 75g of glucose
|
No Intervention: Control
The control intervention consists of quiet sitting for 15 min
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Peak blood glucose concentration
Time Frame: throughout the study, an expected average of 2 weeks per participant
|
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
|
area under the glucose-time curve
Time Frame: throughout the study, an expected average of 2 weeks per participant
|
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
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Christin M. Spengler, Prof., Exercise Physiology Lab, Institute of Human Movement Sciences and Sport, ETH Zurich
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 20, 2020
Primary Completion (Actual)
April 21, 2022
Study Completion (Actual)
April 21, 2022
Study Registration Dates
First Submitted
August 17, 2020
First Submitted That Met QC Criteria
August 19, 2020
First Posted (Actual)
August 20, 2020
Study Record Updates
Last Update Posted (Actual)
March 17, 2023
Last Update Submitted That Met QC Criteria
March 16, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- HOGTT_2020
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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