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Physical ActivityHeartStepsNCT03937674

An mHealth Mobile Application Supporting Maintenance of Physical Activity Among Men and Women With High Blood Pressure

A study testing HeartSteps: A just-in-time intervention for increasing physical activity among sedentary adults. in people with Physical Activity, run by Kaiser Permanente at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of this research is to evaluate the efficacy of contextually tailored activity suggestions and activity planning for increasing physical activity among sedentary adults. Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Physical Activity
What is being tested?
HeartSteps: A just-in-time intervention for increasing physical activity among sedentary adults.
Could I receive a placebo?
No, everyone receives an active treatment
How many people
118 participants
Where
1 siteUnited States
Study dates
1 May 2019to 4 Dec 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • English speaking
  • Recent blood pressure readings that falls in the stage 1 hypertension range by new AHA/ACC guidelines [>= 130 systolic]
  • Owns an iPhone
  • Able to walk for 10 minutes without pain
  • Expresses desire during study screen to increase physical activity

Who cannot join

  • Taking hypertension meds
  • Any diagnosis where physical activity would be counterindicated
  • Recent acute cardio vascular event
  • Major psychiatric illness

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Kaiser Permanente Washington Health Research Institute

    Seattle, Washington, 98101

Other trials in United States

About this study

Official title: Heart Steps: Adaptive mHealth Intervention for Physical-Activity Maintenance

The aim of this research is to evaluate the efficacy of contextually tailored activity suggestions and activity planning for increasing physical activity among sedentary adults.

Read the detailed description

This project file refers to Aim 2 and Aim 3 of the National Heart, Lung, and Blood Institute (NHLBI) grant. Aim 1 is registered in clinical trials.gov under a separate project file number, NCT03225521.

Many of the risk factors for heart disease are behavioral, such as physical inactivity, smoking, and diets high in saturated and trans-fats. Prevention programs are effective at helping patients make the initial lifestyle changes needed to reduce their risks, but patients often struggle to maintain those changes.

In this study the investigators propose to develop a novel mHealth application for supporting maintenance of physical activity. Kaiser Permanente Washington Health Research Institute (KPWHRI) will conduct a prospective study to test the application among Kaiser Permanente Washington (KPW) men and women with blood pressure that falls in the stage 1 hypertension range. By taking advantage of the frequent interactions that individuals have with their mobile phones throughout the day, the investigators will design and evaluate an adaptive, personalized application that (1) keeps patients reminded of their health goals and motivations; (2) provides actionable ideas for how patients can be active right now, given their current context; and (3) helps patients plan and reflect on their physical activity to enable creation of robust and sustainable physical-activity habits. In addition, the application will adapt its functioning for each patient over time in order to minimize user burden while optimizing its ability to encourage physical activity and maintain engagement with the intervention.

Through three Specific Aims-intervention development, intervention optimization, and pilot evaluation-this project will contribute: (1) understanding of how burden and intervention engagement change over time and how they are influenced by intervention delivery and patients' behavior and context; (2) generalization of learning algorithms that are used to personalize web content based on users' characteristics and past behavior for use in mHealth interventions for behavioral maintenance; and (3) new insights about how reflective and automated self-regulatory processes interact over time to support behavioral maintenance and how to optimally recruit these processes through an mHealth intervention.

Aim 2: Optimize intervention and investigate influences on participant response.

The investigators will conduct a three-month micro-randomized pilot study within-subject field study with 40-50 participants with blood pressure readings that fall in the stage 1 hypertension range. Goals for this aim include (1) perform in-situ usability and user-experience testing of the intervention; (2) finalize and tune the intervention's learning algorithms; (3) develop initial decision rules for when and for whom individual intervention components will be provided; and (4) begin to investigate how participants' physical activity, burden, and patterns of engagement with the intervention are affected by different intervention features and the context of use.

Aim 3: Pilot the personalized just-in-time adaptive mHealth intervention over 9 months The investigators will conduct a 9 month-long single-arm pilot study of adaptive mHealth intervention for physical-activity maintenance with 50-60 participants with blood pressure readings that falls in the stage 1 hypertension range. The investigators will (1) evaluate the feasibility and acceptability of the intervention for use over the course of nine months; (2) assess the ability of the learning algorithms to personalize intervention delivery over time; and (3) investigate how cardiac patients' responses to the intervention-physical activity, burden, and engagement-change over time as functions of time-varying application use and time-varying contextual factors. The study will also enable the investigators to gather empirical evidence to plan a follow-up RCT to test the efficacy of the intervention. Development of effective mHealth interventions requires advancements in and collaboration between computer science, human-computer interaction, and behavioral and health sciences. This project makes contributions to all three disciplines and deepens understanding of how to design personalized, adaptive interventions that help individuals not only to adopt but also sustain health-promoting behavior changes over the long-term.

Aim 2 and Aim 3 activities will take place sequentially. The recruitment and participant experience will be almost identical. Differences beyond scientific objectives between the Aim 2 and Aim 3 groups is the time each group is enrolled in the testing trial. Slight modifications are made to materials due to the difference in enrollment time.

No hypotheses will be tested. The purpose of both studies is to develop and test for usability and acceptability of an mHealth application that supports maintenance of physical activity of patients with high blood pressure.

Being tested
HeartSteps: A just-in-time intervention for increasing physical activity among sedentary adults.
Keywords
Physical Activity, Mobile Health, Self Monitoring, Wearable Sensors, Tailored Health Communication, Implementation Intentions, Mobile Apps, Anti-Sedentary Behavior, Opportunistic Physical Activity, Health Belief Model
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • HeartSteps: A just-in-time intervention for increasing physical activity among sedentary adults.Behavioural

    HeartSteps is a smartphone based mHealth intervention that contains the following intervention components: (1) contextually-tailored suggestions for activity; (2) motivational messages aimed at keeping individuals motivated to be active; (3) planning of the next week's activity; and (4) adaptive weekly activity goals. Activity suggestions provide individuals with suggestions for how they can be active, and are tailored based on time of day, user's location, day of the week (weekend/weekday), and weather. Motivational messages are delivered to individuals via a push notification. Activity planning asks users to create a plan of how they will be active in the coming week. Participants are prompted to plan once a week. Each week, as part of the weekly planning, HeartSteps suggests an activity goal for the coming week based on their activity levels the previous week. Participants can edit the suggested goal, and the system-suggested goals top out at 150 minutes of activity per week.

Study groups in NCT03937674
Study groupRoleWhat they receive
HeartSteps InterventionExperimentalFor activity suggestions, at each available decision time, each participant is randomly assigned to either receive an activity suggestion or not.
Receives: Behavioral: HeartSteps: A just-in-time intervention for increasing physical activity among sedentary adults.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 30 minute step count

    step count within the 30-minute window after each available decision point when activity suggestions are randomized. Assessed using the Fitbit Versa Activity tracker.

    Measured: 30 minutes

  2. Daily step count

    Daily step count on the day of treatment. Assessed using the Fitbit Versa activity tracker.

    Measured: 24 hours

Secondary outcomes (1)
  1. MVPA

    Number of minutes of moderate or vigorous physical activity

    Measured: 24 hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 May 2019
  2. Study start1 May 2019
  3. Primary completion30 Nov 2020
  4. Study completion4 Dec 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
At each "decision time"-a time point when an intervention component can be delivered-each day of the study each participant is randomized between intervention or no intervention (delivery of a contextually tailored activity suggestion or no suggestion; morning motivational message or no motivational message)
Masking
None (open label)
Enrolment
118 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03937674
Sponsor's protocol ID
1257484
Acronym
HeartSteps
Status last verified
Oct 2021
First submitted
24 Apr 2019
Last updated
8 Oct 2021
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: A de-identified dataset (i.e., containing no raw location/GPS information) will be generated and made available to the research community. The dataset will be stripped of all codes or any other information that could be linked back to the original data or to an individual participant. Prospective users of this dataset must agree to a confidentiality agreement, meaning that they must get permission from the HeartSteps Primary Investigator to share the data with anyone else. All external requests for data will be directed to Dr. Predrag Klasnja. Prospective investigators will submit a written proposal to the HeartSteps Investigator Team outlining the question they will investigate, the specific variables that they need to answer that question, their analytic plan for answering that question, and documentation of sufficient Institutional Review Board oversight (e.g., approval or exemption). Investigators will also need to sign a confidentiality agreement.

Questions about this trial

What is this clinical trial studying?

A study testing HeartSteps: A just-in-time intervention for increasing physical activity among sedentary adults. in people with Physical Activity, run by Kaiser Permanente at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Oct 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

30 minute step count (time frame: 30 minutes). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Oct 2021.

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