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Responses to Physical Activity Messages Among Midlife Adults

Evaluation of a Tailored Digital Intervention to Promote PA and Reduce CVD Risk Among Women in Midlife

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04711512
Enrollment
30
Registered
2021-01-15
Start date
2021-04-08
Completion date
2022-01-31
Last updated
2022-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise, Motivation, Sedentary Behavior

Brief summary

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).

Detailed description

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.

Interventions

BEHAVIORALEncouragement/Support

Messages that focus on improving self-efficacy and motivation for physical activity

BEHAVIORALSocial Comparison

Messages that provide exposure to another person's physical activity engagement data (for comparison)

Sponsors

Rowan University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Adult age 40-60 years old * Sedentary (\<150 minutes of moderate-intensity or 75 minutes of vigorous-intensity physical activity a week) * One or more cardiovascular risk conditions (i.e., smoking, diagnoses of obesity. prediabetes/type 2 diabetes, prehypertension/hypertension, high cholesterol, metabolic syndrome) * English language fluency * Own a personal smartphone * Have no medical or psychiatric contraindications to changing their physical activity (e.g., current injury, substance use disorder)

Exclusion criteria

* Not an adult age 40-60 years * Not sedentary (≥150 minutes of moderate-intensity or 75 minutes of vigorous-intensity physical activity a week) * No health conditions listed above (smoking, diagnoses of obesity, prediabetes/type 2 diabetes, prehypertension/hypertension, high cholesterol, metabolic syndrome) * No English language fluency * Does not own a personal smartphone * Has medical or psychiatric contraindications to changing their physical activity (e.g., current injury, substance use disorder)

Design outcomes

Primary

MeasureTime frameDescription
Number of stepsup to 24 weeksAssessed via pedometer
Number of minutes in moderate-to-vigorous activityup to 24 weeksAssessed via pedometer
Number of minutes spent sedentaryup to 24 weeksAssessed via pedometer

Secondary

MeasureTime frameDescription
Motivation for physical activityup to 24 weeksAssessed via single self-report item

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026