Physical Activity
Conditions
Keywords
Walking programs, Physical Activity, Behavior Modification, Social Support
Brief summary
The investigators propose a randomized controlled trial based on the Social Networks for Activity (SNAP) Model to evaluate: (1) the effectiveness of an internet-based fitness walking program delivered to patients with risk factors for cardiovascular disease and stroke; and (2) the contribution of social support networks to enhancing the effectiveness of the internet-based fitness walking program. The investigators will recruit 308 patients who are sedentary and have risk factors for cardiovascular disease and randomly assign them to one of the following groups: 1. Internet-based fitness walking program (WalkLink); 2. Internet-based fitness walking program plus additional social network intervention (WalkLink+); and 3. Minimal treatment control. The primary specific aims of this study are to: 1. Evaluate the effects of WalkLink and WalkLink+ relative to a minimal treatment control group on change in: physical activity, aerobic fitness, blood pressure, body composition, and body mass index (BMI), from baseline to posttest, and at 6-month follow-up. 2. Compare the differential effectiveness of WalkLink+ to WalkLink on change in: physical activity, aerobic fitness, blood pressure, body composition and BMI from baseline to posttest, and at 6-month follow-up. 3. Evaluate the mediator and moderator effects of selected individual-level self-management skills (goal setting, planning, self-monitoring), social support variables (number of activity partners, social cues for walking, social praise/reinforcement), and physical-ecological variables (neighborhood walkability, physical cues for walking) on WalkLink and WalkLink+ treatment outcomes.
Interventions
Walking programs with various levels of support will be administered to determine which one is most effective.
Sponsors
Study design
Eligibility
Inclusion criteria
* Sedentary, defined as less than 150 minutes per week of moderate intensity activity * Between the ages of 35 and 64 * Able to speak English * Able to provide informed consent * Able to participate in moderate-intensity physical activity (e.g., moderate pace walking)
Exclusion criteria
* No access to home or private work computer with Internet access * Body mass index (BMI) greater than 39.9 * Systolic blood pressure \> 160 mm Hg or diastolic blood pressure \> 100 mm Hg * Bone, joint, or foot problems that interfere with walking * Diabetes, pulmonary, or cardiovascular disease * Consume 5 or more drinks of alcohol a day * Currently pregnant * Not living within the preselected study neighborhoods or plan to move from the local area during the study period
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Moderate Vigorous Activity | 9 months | Change in Moderate Vigorous Activity will be assessed using Actigraph accelerometers |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Health Risk Factors | 9 months | Aerobic fitness, blood pressure, body mass index, body composition |
Other
| Measure | Time frame | Description |
|---|---|---|
| Environmental Factors | 9 months | Built and social environment factors |
Countries
United States