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Inspiratory Muscle Strength Training in Adults With Type 2 Diabetes (DIT)

Primary Purpose

Diabetes Mellitus, Type 2, Hypertension

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Inspiratory muscle strength training (IMST)
Sponsored by
University of Arizona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Diabetes Mellitus, Type 2 focused on measuring insulin sensitivity, blood pressure, blood glucose, non-pharmacological, inspiratory resistance training

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: diagnosed with type 2 diabetes by physician fasting plasma glucose levels ≥126 mg/dl and ≤240 mg/dl systolic blood pressure between 120-169 mmHg stable dose of medication (three months on the same dose) weight stable in the prior 3 months (<3.0 kg weight change) and willing to remain weight stable throughout the study absence of unstable clinical disease as determined by medical history Exclusion Criteria: current smoker (including tobacco products, vaping devices, THC, etc…) have an uncontrolled medical condition (e.g., cancer) myocardial infarction or stroke within the previous 12 months performs regular aerobic exercise (>4 bouts/week) BMI ≥ 40 kg/m2 systolic blood pressure <120 or ≥170 mmHg diastolic blood pressure >100 or <60 mmHg Cheyne-Stokes respiration history of perforated eardrum history of glaucoma or retinopathy history of collapsed lung diagnosed with asthma pregnant, breastfeeding, or trying to become pregnant (self-reported) medications that, in the opinion of the study physician or nurse practitioner, may impact the outcomes of the study (e.g., steroids)

Sites / Locations

  • Arizona Respiratory and Neurophysiology Laboratory

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

High-resistance IMST

Low-resistance IMST

Arm Description

30 breaths/day (5 sets of 6 breaths, one minute of rest between sets), 5 days/week, 6 weeks

30 breaths/day (5 sets of 6 breaths, one minute of rest between sets), 5 days/week, 6 weeks

Outcomes

Primary Outcome Measures

Change from baseline fasting blood plasma glucose after 6 weeks of IMST
A blood sample will be collected after 12 hours of fasting. Blood and plasma will be separated and plasma glucose levels will be quantified.
Change from baseline fasting blood plasma Insulin after 6 weeks of IMST
A blood sample will be collected after 12 hours of fasting. Blood and plasma will be separated and plasma insulin levels will be quantified.
Change from baseline insulin sensitivity after 6 weeks of IMST
A blood sample will be collected after 12 hours of fasting. Insulin sensitivity will be calculated using the homeostatic model assessment of insulin resistance (HOMA-IR): (fasting serum insulin (mU/L) × fasting plasma glucose (mmol/L) × 22.5).

Secondary Outcome Measures

Change from baseline systolic blood pressure after 6 weeks of IMST
Change in systolic blood pressure (SBP) will be measured by both relative and absolute changes from baseline. SBP will be assessed in accordance with American College of Cardiology/American Heart Association guidelines. Measurements will be taken using an automated oscillometric sphygmomanometer and will be performed in triplicate over the brachial artery of the left arm after 5 minutes of quiet rest, with 1 minute of recovery between measures. SBP will be defined as the average of the 3 pressures.
Change from baseline Nitric Oxide-mediated Endothelial Dependent Dilation (EDD)
Brachial artery Flow Mediated Dilation (BA-FMD), a well-established measure of NO-mediated endothelial function, will be measured by both relative and absolute changes from baseline. BA-FMD will be determined using high-resolution ultrasonography and analyzed with a commercially available software package. An ultrasound probe will be placed 3-6 cm proximal to the antecubital crease on the right arm and a baseline image of the right brachial artery will be obtained. Following baseline, reactive hyperemia will be produced by inflating a rapid-inflating blood pressure cuff. Brachial artery diameter change will be measured for 2 minutes following 5-min of forearm blood flow occlusion.

Full Information

First Posted
November 30, 2022
Last Updated
May 8, 2023
Sponsor
University of Arizona
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1. Study Identification

Unique Protocol Identification Number
NCT05643768
Brief Title
Inspiratory Muscle Strength Training in Adults With Type 2 Diabetes
Acronym
DIT
Official Title
Effects of Inspiratory Muscle Strength Training on Metabolic and Cardiovascular Health in Adults With Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 2023 (Anticipated)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Arizona

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
This clinical research study will investigate the effects of 6 weeks of inspiratory muscle strength training on metabolic and cardiovascular outcomes in adults with recent-onset type 2 diabetes.
Detailed Description
Type 2 diabetes mellitus (T2DM) is at epidemic proportions in the United States and worldwide. It is a chronic obesity-associated metabolic disorder characterized by glucose dysregulation combined with insulin resistance and beta-cell defects. First-line T2DM treatments include lifestyle remedies, such as dietary modifications and exercise. Exercise, whether aerobic and/or resistance training, increases whole-body insulin sensitivity and stimulates muscle glucose uptake independent of insulin. The acute effects of exercise on muscle in patients with abnormal glucose regulation produce immediate improvements in blood glucose levels. In addition, when exercise is repeated over time, adaptations occur that include more long-lasting increases in insulin sensitivity. The effects of traditional exercise on glycemic control and insulin sensitivity in patients with T2DM are well established. However, adherence to traditional exercise programs is low, in part, due to lack of time and physical discomfort, and new regimens for T2DM treatment are needed. Recently, a novel time-efficient respiratory exercise called Inspiratory Muscle Strength Training (IMST) was developed. IMST is distinct from other traditional forms of exercise as it is only 5 minutes per session and performed on a hand-held device during stationary sitting or standing. Typically, IMST comprises 5 sets of 6 inspiratory maneuvers with 1-minute rests between sets. Previous studies demonstrate that 6 weeks of IMST improve systolic blood pressure (SBP), sympathetic nervous system activity, and endothelial function in healthy individuals, middle-aged and older people, and adults with obstructive sleep apnea. These BP-lowering effects of IMST are significant for reducing the risks of cardiovascular disease (CVD), the number one cause of death in people living with diabetes. IMST is safe and tolerable, with adherence rates >90% in diverse populations, and presents a manageable program for improving metabolic health in T2DM patients who have difficulty maintaining a traditional exercise program requiring a large amount of time and physical exertion. It is unknown if IMST, a highly-abbreviated respiratory exercise that is not physically demanding, has beneficial effects on glycemic control and insulin sensitivity, in combination with its improvements on BP measures, in patients with T2DM. The potential for IMST to exert metabolic benefits in diabetic patients warrants assessment

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Hypertension
Keywords
insulin sensitivity, blood pressure, blood glucose, non-pharmacological, inspiratory resistance training

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomly allocated using a 1:1 ratio to A) High-Intensity Training Group (75 % maximal inspiratory pressure) or B)Low-Intensity Training Group (15% maximal inspiratory pressure)
Masking
Participant
Masking Description
This is a randomized trial and participants will be blinded to their allocation group.
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
High-resistance IMST
Arm Type
Experimental
Arm Description
30 breaths/day (5 sets of 6 breaths, one minute of rest between sets), 5 days/week, 6 weeks
Arm Title
Low-resistance IMST
Arm Type
Active Comparator
Arm Description
30 breaths/day (5 sets of 6 breaths, one minute of rest between sets), 5 days/week, 6 weeks
Intervention Type
Behavioral
Intervention Name(s)
Inspiratory muscle strength training (IMST)
Other Intervention Name(s)
inspiratory resistance training, vascular conditioning exercise, inspiratory muscle training
Intervention Description
30 breaths/day, 5 days/week, 6 weeks
Primary Outcome Measure Information:
Title
Change from baseline fasting blood plasma glucose after 6 weeks of IMST
Description
A blood sample will be collected after 12 hours of fasting. Blood and plasma will be separated and plasma glucose levels will be quantified.
Time Frame
Blood plasma collected and analyzed at baseline and after 6 weeks of training
Title
Change from baseline fasting blood plasma Insulin after 6 weeks of IMST
Description
A blood sample will be collected after 12 hours of fasting. Blood and plasma will be separated and plasma insulin levels will be quantified.
Time Frame
Blood plasma collected and analyzed at baseline and after 6 weeks of training
Title
Change from baseline insulin sensitivity after 6 weeks of IMST
Description
A blood sample will be collected after 12 hours of fasting. Insulin sensitivity will be calculated using the homeostatic model assessment of insulin resistance (HOMA-IR): (fasting serum insulin (mU/L) × fasting plasma glucose (mmol/L) × 22.5).
Time Frame
Blood plasma collected and analyzed at baseline and after 6 weeks of training
Secondary Outcome Measure Information:
Title
Change from baseline systolic blood pressure after 6 weeks of IMST
Description
Change in systolic blood pressure (SBP) will be measured by both relative and absolute changes from baseline. SBP will be assessed in accordance with American College of Cardiology/American Heart Association guidelines. Measurements will be taken using an automated oscillometric sphygmomanometer and will be performed in triplicate over the brachial artery of the left arm after 5 minutes of quiet rest, with 1 minute of recovery between measures. SBP will be defined as the average of the 3 pressures.
Time Frame
Blood pressure will be assessed at baseline and after 6 weeks of training
Title
Change from baseline Nitric Oxide-mediated Endothelial Dependent Dilation (EDD)
Description
Brachial artery Flow Mediated Dilation (BA-FMD), a well-established measure of NO-mediated endothelial function, will be measured by both relative and absolute changes from baseline. BA-FMD will be determined using high-resolution ultrasonography and analyzed with a commercially available software package. An ultrasound probe will be placed 3-6 cm proximal to the antecubital crease on the right arm and a baseline image of the right brachial artery will be obtained. Following baseline, reactive hyperemia will be produced by inflating a rapid-inflating blood pressure cuff. Brachial artery diameter change will be measured for 2 minutes following 5-min of forearm blood flow occlusion.
Time Frame
EDD will be assessed at baseline and after 6 weeks of training
Other Pre-specified Outcome Measures:
Title
Change from baseline proteomic analysis
Description
Isolated plasma proteins will be subjected to sequential in-solution digestion (Lys-C and trypsin) followed by analysis with tandem mass spectrometry for pre/post changes. Quantitative proteomics using extracted ion abundance, including statistical analysis, will be performed in Progenesis. The resulting quantitative proteomic data sets will be analyzed using DAVID (david.ncifcrf.gov), a well-established tool for gene ontology enrichment analysis.
Time Frame
Proteomics will be performed at baseline and after 6 weeks of training

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosed with type 2 diabetes by physician fasting plasma glucose levels ≥126 mg/dl and ≤240 mg/dl systolic blood pressure between 120-169 mmHg stable dose of medication (three months on the same dose) weight stable in the prior 3 months (<3.0 kg weight change) and willing to remain weight stable throughout the study absence of unstable clinical disease as determined by medical history Exclusion Criteria: current smoker (including tobacco products, vaping devices, THC, etc…) have an uncontrolled medical condition (e.g., cancer) myocardial infarction or stroke within the previous 12 months performs regular aerobic exercise (>4 bouts/week) BMI ≥ 40 kg/m2 systolic blood pressure <120 or ≥170 mmHg diastolic blood pressure >100 or <60 mmHg Cheyne-Stokes respiration history of perforated eardrum history of glaucoma or retinopathy history of collapsed lung diagnosed with asthma pregnant, breastfeeding, or trying to become pregnant (self-reported) medications that, in the opinion of the study physician or nurse practitioner, may impact the outcomes of the study (e.g., steroids)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dallin Tavoian, PhD
Phone
520-621-0388
Email
tavoian@arizona.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dallin Tavoian, PhD
Organizational Affiliation
University of Arizona
Official's Role
Principal Investigator
Facility Information:
Facility Name
Arizona Respiratory and Neurophysiology Laboratory
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85724
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to make IPD available
Citations:
PubMed Identifier
36107991
Citation
Craighead DH, Tavoian D, Freeberg KA, Mazzone JL, Vranish JR, DeLucia CM, Seals DR, Bailey EF. A multi-trial, retrospective analysis of the antihypertensive effects of high-resistance, low-volume inspiratory muscle strength training. J Appl Physiol (1985). 2022 Oct 1;133(4):1001-1010. doi: 10.1152/japplphysiol.00425.2022. Epub 2022 Sep 15.
Results Reference
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Inspiratory Muscle Strength Training in Adults With Type 2 Diabetes

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