University of Toronto
Toronto, Ontario, M5S 2C9, Canada
Location status: Recruiting
Location contact
Amy A. Kirkham, PhD
CONTACT
Jenna B. Gillen, PhD
CONTACT
NCT Number: NCT06345937
This study aims to produce new evidence, specific to women, on the efficacy and mechanisms of exercise and diet for cardiometabolic risk reduction in pre and postmenopausal women. Using a 3-arm randomized controlled trial (RCT) with equal recruitment and stratification by menopausal status to 6 months of: 1) exercise following Health Canada guidelines; 2) the same exercise plus counselling to follow Canada's Dietary Guidelines to improve diet quality; or 3) stretching group, this study will answer the following questions:
* How does the impact of exercise compare among each of the causal links between physical inactivity and cardiometabolic disease in women? * What is the effect modification of adding a diet quality intervention to exercise? * What is the effect modification by menopausal status?
The investigators hypothesize that exercise adaptations will be: 1) largest peripherally, including Matsuda index (primary outcome), Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), arteriovenous oxygen difference (avO2diff), and visceral fat, compared to centrally (stroke volume (SV), endothelial function, aortic stiffness), 2) blunted or absent in post vs premenopause; 3) enhanced by the addition of diet quality which will be essential or additive for Matsuda index, metabolic syndrome, Framingham cardiovascular disease (CVD) risk, cytokines and adipokines, thigh myosteatosis, muscle mass, peak oxygen uptake (VO2peak), 4) enhanced by adding diet quality in more outcomes postmenopause.
Interested in participating?
Request Info30 year and older
Female
Interventional
Not applicable
Toronto, Ontario, M5S 2C9, Canada
Location status: Recruiting
Amy A. Kirkham, PhD
CONTACT
Jenna B. Gillen, PhD
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Through a combination of exercise trainer-led in-person and virtual sessions, as well as counselling for independent aerobic exercise, participants will be guided to achieve 150 weekly minutes of moderate-intensity aerobic activity and twice weekly whole-body muscle strengthening.
Behavioural Experimental: guidelines-based physical activity:
Through a combination of exercise trainer-led in-person and virtual sessions, as well as counselling for independent aerobic exercise, participants will be guided to achieve 150 weekly minutes of moderate-intensity aerobic activity and twice weekly whole-body muscle strengthening.
Behavioural Experimental: guidelines-based healthy eating:
One-on-one phone/virtual counselling from a registered dietitian to change dietary habits to be in line with Canada's Food Guide.
Twice weekly virtual instructor-led whole-body stretching.
Time frame: 6 months
As assessed by the Matsuda Index calculated from an oral glucose tolerance test (OGTT).
Time frame: 6 months
Indirectly measured via HOMA-IR using fasting glucose and insulin levels
Time frame: 6 months
Calculated as a z-score to allow for tracking change in the interventions
Time frame: 6 months
Calculated using a widely-used standardized scoring system
Time frame: 6 months
Measured as peak volume of oxygen consumption via indirect calorimetry during a cardiopulmonary exercise test on a treadmill.
Time frame: 6 months
Measured as the difference between peak heart rate during the cardiorespiratory fitness test and heart rate 2-minutes after stopping the exercise test.
Time frame: 6 months
Measured during submaximal and maximal periods of a cycling exercise test, using echocardiography.
Time frame: 6 months
Measured during rest, submaximal and maximal periods of cycling exercise test, using echocardiography
Time frame: 6 months
Measured via echocardiography at rest
Time frame: 6 months
Measured using two methods: (1) calculated as the volume of oxygen (VO2) from the corresponding workload from the day 1 treadmill test divided by cardiac output at rest, submaximal, and maximal periods of the cycling exercise test; and (2) direct assessment using near-infrared spectroscopy as a measure of tissue oxygenation in the legs at rest, submaximal, and maximal periods of the cycling exercise test.
Time frame: 6 months
Measured using a brachial artery flow-mediated dilation test using ultrasound.
Time frame: 6 months
Measured using a common carotid artery image using ultrasound.
Time frame: 6 months
Measured as the pulse wave velocity of the central (carotid-femoral) and peripheral leg (femoral-dorsalis pedis) and arm (carotid-radial) regions. Blood pressure may be added as covariate in analysis of arterial stiffness.
Time frame: 6 months
Measured as the average of the last 5 of 6 blood pressure measurements using an automatic blood pressure device.
Time frame: 6 months
Assessed using a 3-lead electrocardiogram in the supine position for 10 minutes after a 5-minute supine rest.
Time frame: 6 months
Measured as thigh muscle fat fraction (percent of muscle compartment composed of fat pixels) determined from contiguous axial fat-water separation 3 Tesla (3T) magnetic resonance images of both thighs.
Time frame: 6 months
Measured using an isokinetic dynamometer (Biodex) to assess peak torque and total work in 30 repetitions of knee flexion.
Time frame: 6 months
Measured determined from contiguous axial fat-water separation 3T magnetic resonance images of both thighs
Time frame: 6 months
Measured via western blotting from a skeletal muscle biopsy of the vastus lateralis muscle. Proteins of interest include those found in mitochondria, contractile signaling pathways, insulin signaling pathways, and in glucose and fat metabolism.
Time frame: 6 months
Measured via immunofluorescence from a skeletal muscle biopsy of the vastus lateralis muscle. Outcomes of interest include skeletal muscle capillarization, lipid content, and fiber type and cross sectional area.
Time frame: 6 months
Measured via spectrophotometer to assess the maximal enzyme activity of enzymes involved in skeletal muscle oxidative capacity, from a biopsy of the vastus lateralis muscle.
Time frame: 6 months
Measured using a body composition device (BodPod) to estimate whole body fat (in kg and %) and fat free mass (in kg and %).
Time frame: 6 months
Volumes of adipose tissue in the visceral region measured using 3T fat-water separation magnetic resonance imaging
Time frame: 6 months
Measured as percent of liver volume composed of fat pixels determined from 3 slices through the middle of the liver using the PROFIT1 3T magnetic resonance images sequence.
Time frame: 6 months
Circumferences of the waist, hip and neck, measured using an inelastic tape
Time frame: 6 months
Assessments from blood including leptin, adiponectin, Tumour Necrosis Factor alpha (TNF-a), Interleukin-6 (IL-6), C-reactive protein (CRP). These measures have been grouped together as the markers will be considered together when interpreted.
Time frame: 6 months
Analyzed from blood serum using a clinical assay at a core lab.
Time frame: 6 months
Analyzed from blood plasma using a clinical assay at a core lab.
Time frame: 3 months, 6 months, 12 months
Various components of dietary intake including macronutrients and micronutrients will be assessed through 3-day food records over 2 weekdays and 1 weekend collected using Automated Self-Administered 24hour (ASA-24) online system.
Time frame: 6 months
Assessment of ALT, AST, and albumin via a fasting blood serum draw, analyzed on a clinical assay at a core lab.
Time frame: 6 months
Liver T1 time evaluated using the PROFIT1 magnetic resonance sequence, validated marker of liver fibrosis.
Time frame: 6 months, 12 months
Average adherence to prescribed aerobic physical activity weekly minutes measured via Garmin smart watch
Time frame: 6 months, 12 months
Average adherence to prescribed resistance exercise activity weekly sessions via an attendance log
Time frame: 3 months, 6 months, 12 months
An overall measure of alignment with the dietary guidelines measured via the Canadian healthy eating index calculated from 3-day diet records
Time frame: 3 months, 6 months, 12 months
Assessed by RAND-36, where an independent score is provided for 8 scales ranging from 0 to 100 and 2 component summary scales ranging from 0-50 with a higher score indicating better quality of life.
Time frame: 3 months, 6 months, 12 months
Assessed by the Menopause-specific Quality of Life (MENQOL) questionnaire. Each of four domains is constrained between 1 to 8 where a higher score indicates more symptoms.
Time frame: 3 months, 6 months, 12 months
Assessed by the perceived stress scale (PSS-14) where individual scores can range from 0 to 56 with higher scores indicating higher perceived stress
Time frame: 3 months, 6 months, 12 months
Measured by the Hospital Anxiety and Depression Scale (HADS); score ranges from 0-21 for each of depression and anxiety with a higher score indicating more severe depression or anxiety
Time frame: 3 months, 6 months, 12 months
Assessed by the barriers to self-efficacy scale (BARSE). For each item, participants indicate their confidence to execute the behavior on a 100-point percentage scale comprised of 10-point increments, ranging from 0% (not at all confident) to 100% (highly confident). Total strength for each measure of self-efficacy is then calculated by summing the confidence ratings and dividing by the total number of items in the scale, resulting in a maximum possible efficacy score of 100.
Time frame: 3 months, 6 months, 12 months
Assessed via the multi-process action control approach, which is a series of questionnaires developed to understand affective attitudes, instrumental attitudes, perceived capability over physical activity, perceived opportunity for physical activity, decisional intentions, behavioural regulation, physical activity habits, and identity around physical activity. Higher scores represent better physical activity motivations. (Reference: Rhodes, R.E. (2017). The evolving understanding of physical activity behavior: A multi-process action control approach. In A. J. Elliot (Ed), Advances in Motivation Science. (pp. 171-205).)
Time frame: 3 months, 6 months, 12 months
Subjectively assessed by the Pittsburgh Sleep Quality Index (PQSI), which measures components of sleep: sleep duration, disturbance, sleep latency, daytime dysfunction due to sleepiness, sleep efficiency, overall sleep quality, and sleep medication use, with higher scores reflecting poorer sleep quality.
Time frame: 3 months, 6 months, 12 months
Measured via Garmin smart watch for the total sleep duration and efficiency.
Time frame: 3 months, 6 months, 12 months
Assessed by the Recent Physical Activity Questionnaire (RPAQ) that collects information about types and amounts of activity (sedentary and physical activities) over the last 3 months in the following domains: leisure time, occupation, commuting, domestic life, with greater scores indicating longer time engaging in forms of activity.
Time frame: 6 months
Assessed using fasting blood serum in a clinical assay.
Time frame: 6 months
Assessed using a salivary sample in-house using a clinical assay.
Time frame: 6 months
Assessed using a fasting blood plasma sample in a clinical assay at a core lab.
Time frame: 6 months
Assessed using fasting blood serum in a clinical assay.
Time frame: 6 months
Assessed using a calibrated scale attached to the BodPod body composition device.
Time frame: 6 months
Calculated from a measurement of height using a stadiometer and body weight (detailed above).
Time frame: 3 months, 6 months, 12 months
Energy balance will be quantified as: 3-day avg calorie intake - [estimated resting metabolic rate + 3-day avg Garmin estimate of physical activity energy expenditure + 10% of calorie intake (thermic effect of food)].
Contact information is provided by the study sponsor or research team.
Amy A. Kirkham, PhD
CONTACT
Jenna B. Gillen, PhD
CONTACT
University of Toronto
Other
Acronym: MsFIT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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