Exercise Snacks in Obesity
ObesityTo conduct a randomized control trial to determine the feasibility and preliminary efficacy of a 12-week technology-enabled exercise snacks intervention with behaviour change counselling for improving cardiorespiratory fitness and various markers of cardiometabolic health in previously inactive adults living with obesity.
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Conditions de participation
-
Sexe:
ALL -
Âges admissibles:
35 to 64
Critères de participation
Inclusion Criteria:
* Aged 35-64 years.
* Habitually engaging in \< 150 min moderate-to-vigorous physical activity per week.
* Body mass index 30-45 kg/m2 or 27.5-45 for participants who self-identify as being of Asian or Southeast Asian origin.
* Waist circumference: \>88cm for females and \>102cm for males, or \>80 cm for females and \>90 cm for male participants who self-identify as being of Asian or Southeast Asian.
* Not currently diagnosed with a cardiometabolic disease (e.g., coronary artery disease, stroke, diabetes, non-alcoholic fatty liver disease).
* Taking ≤2 commonly prescribed medications for the prevention of cardiometabolic diseases (e.g., statins, antihypertensives).
* Not a current smoker
* Cleared to engage in physical activity using the Get Active Questionnaire and, if applicable, consultation with a health care provider or Qualified Exercise Professional.
* Access to a computer, tablet or smartphone for intervention delivery and tracking.
* Ability to read and write in English.
Exclusion Criteria:
* Chronic musculoskeletal condition or recent (within 2 years) cardiovascular event preventing participation in exercise.
* Lack of internet access.
* Angina upon exertion assessed by the Rose Angina Questionnaire.
* Prescribed beta-blockers that can compromise the validity of heart rate measurements. during the exercise test.
* Have a scheduled surgical procedure within the next 3-4 months that would prevent exercise participation.
* Currently participating in another clinical trial that interferes with the study procedures.
* Currently pregnant or planning on becoming pregnant during the intervention (i.e., within the next 4 months).
* Uncontrolled high blood pressure (\>160/90 mmHg)
Lieu de l'étude
McMaster University
McMaster UniversityHamilton, Ontario
Canada
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University of British Columbia Okanagan
University of British Columbia OkanaganKelowna, British Columbia
Canada
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- Étude parrainée par
- University of British Columbia
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT06924346