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OpenTrials
Completed

NCT Number: NCT04711512

Responses to Physical Activity Messages Among Midlife Adults

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).

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Key information

Age range

40 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Rowan University

Glassboro, New Jersey, 08028, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Encouragement/Support

Behavioral

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

Social Comparison

Behavioral

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

Primary outcomes

  1. Number of steps

    Time frame: up to 24 weeks

    Assessed via pedometer

  2. Number of minutes in moderate-to-vigorous activity

    Time frame: up to 24 weeks

    Assessed via pedometer

  3. Number of minutes spent sedentary

    Time frame: up to 24 weeks

    Assessed via pedometer

Secondary outcomes

  1. Motivation for physical activity

    Time frame: up to 24 weeks

    Assessed via single self-report item

Sponsors and collaborators

Lead sponsor

Rowan University

Other

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Jan 15, 2021
Registry last updated
Apr 28, 2022

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.

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