The Effect of Hypoxia on Type 2 Diabetes and Weight Loss
Primary Purpose
Type2 Diabetes
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Sleeping in a tent
Sponsored by
About this trial
This is an interventional other trial for Type2 Diabetes
Eligibility Criteria
Inclusion Criteria:
- Males and post-menopausal women with T2DM (as diagnosed with the WHO criteria).
Exclusion Criteria:
- Individuals with contraindications to hypoxic exposure (e.g. obstructive sleep apnoea, extant cardiac conditions or on medications such as SGLT2 inhibitors or PPAR antagonists).
Sites / Locations
- Anthony Shepherd
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Hypoxia - 15% O2
Sham - room air 21% 02
Arm Description
Participants will sleep in a tent for 10 nights.
Participants will sleep in a tent for 10 nights.
Outcomes
Primary Outcome Measures
Mean AUC (Area Under the Curve) Plasma [Glucose]
Does 10 days of overnight hypoxia change AUC during a oral glucose tolerance test. Units for AUC are AU (arbitrary units) which have been derived from the trapezoidal method and have been published as such. Trapezoidal method: AUC = Δx ((y0/2)+y1+y2+y3+...+(yn/2)).
Secondary Outcome Measures
Reduce body mass
Does 10 days of overnight hypoxia change body mass - assessed via DXA.
Redox balance (via ELISA)
Does 10 days of overnight hypoxia change redox balance (IL-6, nitrite, TNFɑ & SOD)
Total minutes of physical activity (light, moderate, moderate to vigorous physical activity).
Does 10 days of overnight hypoxia change physical activity - assessed via wrist worn accelerometery
Sleep efficiency (time in bed + time asleep)
Does 10 days of overnight hypoxia change sleep - assessed via wrist worn accelerometery
Full Information
NCT ID
NCT05147116
First Posted
November 8, 2021
Last Updated
April 20, 2023
Sponsor
University of Portsmouth
Collaborators
Bournemouth University, University College, London, University of Cambridge, Portsmouth Hospitals NHS Trust
1. Study Identification
Unique Protocol Identification Number
NCT05147116
Brief Title
The Effect of Hypoxia on Type 2 Diabetes and Weight Loss
Official Title
The Effects of Repeated Moderate Overnight Normobaric Hypoxia on Glucose Homeostasis, Appetite, Body Weight, Inflammation and Oxidative Stress in Individuals With Type 2 Diabetes Mellitus
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
February 17, 2022 (Actual)
Primary Completion Date
January 30, 2023 (Actual)
Study Completion Date
January 30, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Portsmouth
Collaborators
Bournemouth University, University College, London, University of Cambridge, Portsmouth Hospitals NHS Trust
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The number of people with type 2 diabetes mellitus (T2DM) continuing to rise, this pandemic is expected to reach 700 million people by 2045. T2DM is a metabolic condition characterized by progressive insulin resistance and chronic hyperglycemia (high blood glucose concentrations). Hyperglycaemia increases the risk of both micro- and macrovascular damage, whilst interventions that reduce blood glucose mitigate this risk. Weight loss, achieved through exercise and dietary modification, is effective at reducing hyperglycaemia. However, despite the clear benefits of exercise and weight loss, diverse psychological, sociological and logistical factors can make it difficult for some individuals with T2DM to initiate, or adhere to, these lifestyle interventions. Alternative approaches to treatment are therefore required.
The purpose of this research project is to investigate whether 10-days of overnight exposure to moderate hypoxia is effective at improving blood glucose control in individuals with T2DM and to provide insight into the physiological mechanisms responsible for any beneficial effects.
Detailed Description
Type 2 diabetes mellitus (T2DM) is a metabolic condition characterized by progressive insulin resistance and chronic hyperglycemia (high blood glucose concentrations). Hyperglycaemia increases the risk of both micro- and macrovascular damage, whilst interventions that reduce blood glucose mitigate this risk. Weight loss, achieved through exercise and dietary modification, is effective at reducing hyperglycaemia. However, despite the clear benefits of exercise and weight loss, diverse psychological, sociological and logistical factors can make it difficult for some individuals with T2DM to initiate, or adhere to, these lifestyle interventions. With the number of people with T2DM continuing to rise, this pandemic is expected to reach 700 million people by 2045. Thus, there is a clear need for cost-effective interventions that can effectively improve glycaemic control in people with T2DM and which people will adhere to.
A simple exposure to a lowered concentration of inspired oxygen (i.e. hypoxia) may represent such an intervention. In addition to the beneficial effects on glucose homeostasis that have been reported following a single acute hypoxic exposure, repeated intermittent, or continuous, hypoxic exposure may also have therapeutic potential in individuals with T2DM. In rodent models, daily hypoxic exposures returned fasting blood [glucose] to normal levels and increased glucose transporter 4 translocation in mice with T2DM. Similar effects on glucose homeostasis have been shown in overweight humans and those with insulin resistance, (during intermittent hypoxic training) which was explained, at least in part, by reduction in body mass (~ 1.2 kg).
The mechanisms underpinning the improved glycaemic control in response to hypoxia are likely multifactorial. Specifically, our objective is to assess a novel therapeutic intervention for the treatment and management of T2DM which overcomes many of the barriers to uptake and adherence that are associated with some lifestyle interventions such as exercise and weight loss.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type2 Diabetes
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Single blind, randomized, balanced, crossover design study
Masking
Participant
Masking Description
Participants will undergo both the hypoxia and sham conditions and will be blinded to the conditions in which they are in.
Allocation
Randomized
Enrollment
13 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hypoxia - 15% O2
Arm Type
Experimental
Arm Description
Participants will sleep in a tent for 10 nights.
Arm Title
Sham - room air 21% 02
Arm Type
Sham Comparator
Arm Description
Participants will sleep in a tent for 10 nights.
Intervention Type
Other
Intervention Name(s)
Sleeping in a tent
Intervention Description
Participants will spend 10 consecutive nights of sleeping in a tent
Primary Outcome Measure Information:
Title
Mean AUC (Area Under the Curve) Plasma [Glucose]
Description
Does 10 days of overnight hypoxia change AUC during a oral glucose tolerance test. Units for AUC are AU (arbitrary units) which have been derived from the trapezoidal method and have been published as such. Trapezoidal method: AUC = Δx ((y0/2)+y1+y2+y3+...+(yn/2)).
Time Frame
Assessed on all outcome visits (2,3,4&5) across an 8 week period.
Secondary Outcome Measure Information:
Title
Reduce body mass
Description
Does 10 days of overnight hypoxia change body mass - assessed via DXA.
Time Frame
Assessed on all outcome visits (2,3,4&5) across an 8 week period.
Title
Redox balance (via ELISA)
Description
Does 10 days of overnight hypoxia change redox balance (IL-6, nitrite, TNFɑ & SOD)
Time Frame
Assessed on all outcome visits (2,3,4&5) across an 8 week period.
Title
Total minutes of physical activity (light, moderate, moderate to vigorous physical activity).
Description
Does 10 days of overnight hypoxia change physical activity - assessed via wrist worn accelerometery
Time Frame
Assessed on all outcome visits (2,3,4&5) across an 8 week period.
Title
Sleep efficiency (time in bed + time asleep)
Description
Does 10 days of overnight hypoxia change sleep - assessed via wrist worn accelerometery
Time Frame
Assessed on all outcome visits (2,3,4&5) across an 8 week period.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Males and post-menopausal women with T2DM (as diagnosed with the WHO criteria).
Exclusion Criteria:
Individuals with contraindications to hypoxic exposure (e.g. obstructive sleep apnoea, extant cardiac conditions or on medications such as SGLT2 inhibitors or PPAR antagonists).
Facility Information:
Facility Name
Anthony Shepherd
City
Portsmouth
State/Province
Hampshire
ZIP/Postal Code
PO1 2ER
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
The individual data set that is used for statistical analysis will be uploaded to our university repository and a DOI added to the paper upon publication.
IPD Sharing Time Frame
Upon publication - no plan to remove.
Learn more about this trial
The Effect of Hypoxia on Type 2 Diabetes and Weight Loss
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