Health Improvement After Pregnancy (HIP) Program Randomized Control Trial
- Conditions
- Metabolic Cardiovascular Syndrome
- Interventions
- Behavioral: HIP Program
- Registration Number
- NCT02077179
- Lead Sponsor
- Queen's University
- Brief Summary
Recent Canadian studies, public opinion polls and the Canadian Heart Health Strategy and Action Plan state that women's heart health is a key national priority; it should be addressed through improving heart health awareness and prevention, and reducing care inequities for women in general and younger women in particular. The investigators have developed an innovative and interactive mobile website based postpartum lifestyle modification program (regular physical activity and nutritional guidance), based on established national guidelines, to improve heart disease risk factors in women. The investigators will conduct a trial to determine if the mobile website based lifestyle modification program can be maintained and reduces a collection of risk factors, which occurring together, greatly increases the risk of developing heart disease. The investigators hypothesize that the interactive mobile website directing regular physical activity and personalized nutritional guidance, compared to standard postpartum care, will be motivational and result in a reduced modified metabolic syndrome z score at 8 months postpartum among the intervention group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- Female
- Target Recruitment
- 43
- must own or have daily access to one or more of the following; smart phone, tablet or laptop computer
- Living greater than 100km from Kingston General Hospital
- Having an existing and long term contraindication to exercise at the time of recruitment
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description HIP Program HIP Program Participants in this arm will follow the HIP Program in addition to their usual care from Kingston General Hospital and their primary care provider.
- Primary Outcome Measures
Name Time Method Metabolic Syndrome Z Score 32 weeks postpartum The primary outcome measure is the metabolic syndrome (MetS) z score, a continuous score of the five metabolic syndrome variables that make up the Adult Treatment Panel (ATP) III diagnostic criteria (waist circumference, blood pressure, high density lipoprotein, triglycerides and glucose). Differences between study arms will be compared.
- Secondary Outcome Measures
Name Time Method Adherence to the HIP Program; Percent of Workouts Completed 32 weeks postpartum Adherence to the HIP Program will be assessed based on the number of times a participant indicates using the mobile website that a prescribed workout has been completed. This outcome will only be measured in the intervention arm.
Differences in Biochemical Cardiovascular Risk Markers 32 weeks postpartum Differences between study arms for the following biochemical cardiovascular risk markers will be assessed at 32 weeks postpartum; lipid profile, fasting glucose, glycated hemoglobin, high sensitivity C-reactive protein, and urine microalbumin creatinine ratio.
Change in Anthropomorphic Measurements and Blood Pressure from Baseline at Midpoint 20 weeks postpartum Changes in systolic blood pressure, diastolic blood pressure and weight from baseline measures at 6-8 weeks postpartum will be assessed at the midpoint of the program at 20 weeks postpartum. Differences between study arms will be compared.
Change in Anthropomorphic Measurements and Blood Pressure from Baseline at Study Completion 32 weeks postpartum Changes in systolic blood pressure, diastolic blood pressure and weight from baseline measures at 6-8 weeks postpartum will be assessed at the midpoint of the program at 32 weeks postpartum. Differences between study arms will be compared.
Change in Anthropomorphic Measurements and Blood Pressure from Midpoint to Study Completion 32 weeks postpartum Changes in systolic blood pressure, diastolic blood pressure, weight, body mass index, hip circumference, and waist circumference from midpoint measures at 20 weeks postpartum will be assessed at the end of the program at 32 weeks postpartum. Differences between study arms will be compared.
Adherence to the HIP Program; Percent of Step Counting Completed 32 weeks postpartum Adherence to the HIP Program will be assessed based on the number of times a participant uses the mobile website to log their daily step count total. The number of times that the logged step count meets or exceeds the prescribed number of daily steps will also be assessed. This outcome will only be measured in the intervention arm.
Adherence to the HIP Program; Percent of Dietary Logs Completed 32 weeks postpartum Adherence to the HIP Program will be assessed based on the number of times a participant uses the mobile website to enter the weekly dietary log. The number of times that the dietary log meets the prescribed intake for each of the Canada's Food Guide food groups will also be assessed. This outcome will only be measured in the intervention arm.
Trial Locations
- Locations (1)
Queen's Unviersity
🇨🇦Kingston, Ontario, Canada