Rowan University
Glassboro, New Jersey, 08028, United States
NCT Number: NCT04711512
The purpose of this study is to test the short-term effects of physical activity promotion messages designed for midlife adults. These messages are designed to provide information and motivation for physical activity by engaging key social processes, such as social comparison (i.e., self-evaluations relative to others).
Looking for future studies?
Notify Me40 year–60 year
All sexes
Observational
Glassboro, New Jersey, 08028, United States
This study will employ an intensive assessment procedure, in which participants are asked to complete several brief surveys per day via mobile device. On some days, as described below, survey content will be assigned with an embedded experimental design, administered via "micro-randomization" (i.e., randomization to receive one of multiple types of content at each momentary report). These methods allow for insight into the immediate effects of different types of content and their accumulated effects over the study period, as participants go about their normal activities.
Participants will complete an initial survey to assess their global and recent experiences (e.g., demographic information, social media use). Participants then will be asked to engage in 7 days of ambulatory data collection (i.e., as they go about their normal daily activities). This includes wearing pedometers to capture PA behavior (steps per day and aerobic-intensity PA) and completing 4 surveys per day via their smartphone.
A. For the first 3 days, surveys will assess each participant's preferences and responses to potential message content as they naturally occur. Content has been pre-tested in preliminary work. This will establish participants' baseline behaviors.
B. For the following 2 days, participants will be randomized at each survey to either: 1) make an upward PA comparison (to someone engaging in a lot of activity), 2) make a downward PA comparison (to someone engaging in very little activity), or 3) assess a different experience (e.g., received social support).
C. For the final 2 days, participants will be randomized at each survey to either: 1) informational messages about ways to increase activity, 2) encouragement to increase their activity in healthy ways, or 3) reminders about their activity goals.
Phases B and C will be counterbalanced, such that half of participants will receive prompts described in Phase B before Phase C, and half will receive prompts described in Phase C before Phase B.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Messages that focus on improving self-efficacy and motivation for physical activity
Messages that provide exposure to another person's physical activity engagement data (for comparison)
Time frame: up to 24 weeks
Assessed via pedometer
Time frame: up to 24 weeks
Assessed via pedometer
Time frame: up to 24 weeks
Assessed via pedometer
Time frame: up to 24 weeks
Assessed via single self-report item
Rowan University
Other
Evaluation of a Tailored Digital Intervention to Promote PA and Reduce CVD Risk Among Women in Midlife
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.
Published trials that share one or more normalized conditions with this study.
NCT04518943
Behavior, Behavioral Symptoms
Seattle, Washington, United States
View Trial DetailsNCT05455008
Behavior, Behavior and Behavior Mechanisms
Iowa City, Iowa, United States
View Trial DetailsNCT05281978
Adult, Behavior
Urbana, Illinois, United States
View Trial DetailsNCT04498130
Behavior, Cancer Survivors
Urbana, Illinois, United States
View Trial Details