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Feasibility of Aerobic Exercise With Blood Flow Restriction Training in People Living With Type 2 Diabetes
NCT07196371 · University of New Brunswick
In plain English
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Official title
Testing the Feasibility of Blood Flow Restriction Training to Enhance the Health Benefits of Exercise in Individuals With Type 2 Diabetes: a Pilot Randomized Controlled Trial
About this study
Individuals with type 2 diabetes (T2D) display reduced cardiorespiratory fitness, which is a strong predictor of premature mortality and T2D-related complications. Aerobic training (AT) enhances cardiorespiratory fitness and is considered a cornerstone in the management and treatment of T2D. Emerging data suggest that AT combined with blood flow restriction (AT+BFR) training, could potentially enhance cardiorespiratory fitness faster than typical AT in healthy individuals. However, the feasibility of AT+BFR in individuals with T2D and its impact on cardiorespiratory fitness have yet to be determined.
Therefore, the primary objective of this study is to test the feasibility of a 6-week AT+BFR training intervention in individuals with T2D. The secondary objective is to establish preliminary effect sizes for the efficacy of AT+BFR training in individuals with T2D compared to the standard care AT (AT- stdCare).
Methods: This study is a single-blind (investigator \& statistical analyst), multi-site, randomized controlled pilot trial of a novel AT+BFR training intervention for individuals living with T2D, which has been informed by patients with lived experience. Participants will be randomized 1:1 using variable permuted block sizes (stratified by sex and site) into 1) AT+BFR or 2) AT-stdCare groups with outcome measures assessed at baseline and 6 weeks.
Population: In 3 sites across Canada, 60 (n=20 per site) individuals living with T2D (5.7% \< HbA1c \< 9.0%) aged 19-64 years, not meeting the physical activity guidelines (150 mins moderate-vigorous physical activity per week) will be recruited to participate in this 6-week pilot trial.
Intervention: Participants will perform supervised AT+BFR 3 times weekly for 32 minutes per session. A blood pressure cuff will be set between 60-80% of limb arterial occlusion with AT for 96 minutes per week of treadmill walking performed at 40-50% of heart rate reserve (HRR).
Participants in the AT-stdCare will perform 96 minutes per week of treadmill walking at 40-50% of HRR following the same schedule as AT+BFR, training 3 times per week for 32 minutes per session.
Outcomes: The main outcome measures will pertain to the feasibility of a larger trial and include recruitment rates, enrollment and adherence to the intervention, and retention for follow-up testing. The secondary outcomes will be focused on establishing effect sizes to power a larger trial. Effect sizes for the change in cardiorespiratory fitness and continuous glucose monitoring (CGM) outcomes will be determined to help select and power a primary outcome for a more definitive trial of AT+BFR.
Eligibility criteria
Inclusion Criteria:
* Diagnosed with type 2 diabetes (5.7% \< HbA1c \< 9.0%)
* Not regularly physically active (150 mins moderate-vigorous physical activity per week)
Exclusion Criteria:
* Musculoskeletal issues preventing exercise training
* Unstable medications over the last 3 months
* Absolute contraindications to BFR (i.e. peripheral vascular disease)
* A self-reported diagnosis of low iron concentrations, anemia, or being treated for these conditions
* A diagnosis of any red blood cell-altering condition (i.e., sickle cell anemia, poikilocytosis)
* Currently living with any cardiovascular disease, which would impact the ability to participate in exercise safely
* Currently prescribed any medication which would impact the ability to use a heart rate monitor to accurately track intensity
Study design
Enrollment target: 60 participants
Allocation: randomized
Masking: double
Age groups: adult
Timeline
Starts: 2026-01-01
Estimated completion: 2028-12
Last updated: 2026-01-26
Interventions
Behavioral: Aerobic Training with Blood Flow RestrictionBehavioral: Standard Aerobic Training
Primary outcomes
- • Rate of Recruitment (Every 4 weeks up to 2 years)
- • Rate of Enrollment (Every 4 weeks up to 2 years)
- • Adherence to the Intervention (From enrollment to the end of intervention at week 6)
Sponsor
University of New Brunswick · other
With: Diabetes Canada, University of Guelph, University of British Columbia
Contacts & investigators
ContactMartin Senechal, PhD · contact · martin.senechal@unb.ca · 506-451-6889
ContactJamie Burr, PhD · contact · burrj@uoguelph.ca · 519-824-4120
InvestigatorMartin Senechal, PhD · principal_investigator, Cardiometabolic Exercise & Lifestyle Laboratory, Fredericton, New Brunswick
All locations (3)
Exercise Metabolism and Inflammation LaboratoryNot Yet Recruiting
Okanagan, British Columbia, Canada
Cardiometabolic Exercise & Lifestyle LaboratoryRecruiting
Fredericton, New Brunswick, Canada
Human Performance & Health Research LaboratoryRecruiting
Guelph, Ontario, Canada