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App ProficiencyNCT06191822

Aspire2B Personalization Pilot Study Program

A study testing Nutrition, Fitness and Sleep in people with App Proficiency and Behavior, run by PepsiCo Global R&D 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

This non-randomized pilot study program is focused on assessing the technical characteristics of the Aspire2B mobile device application. Read more about this study

Who is it for?
Ages 18 to 75 yearsHealthy volunteers can take part
Conditions the study is for
App Proficiency, Behavior, Lifestyle
What is being tested?
Nutrition, Fitness and Sleep
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,714 participants
Where
1 siteUnited States
Study dates
1 Mar 2022to 1 Sep 2023
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
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Fluent in reading and understanding English or Spanish
  • Smartphone users

Who cannot join

  • Cannot proceed to onboarding without downloading the app, consenting to participate, and agreeing to app Terms of Use

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Remote, no facility visits. Managed by PepsiCo R&D Life Sciences

    Chicago, Illinois, 60661

Other trials in United States

About this study

This non-randomized pilot study program is focused on assessing the technical characteristics of the Aspire2B mobile device application.

Read the detailed description

Aspire2B is a mobile wellness app that uses non-invasive measurements to predict various physiological states and estimate biological age. Users are then enrolled in nutrition, fitness, or sleep challenges within the app that are aimed at improving overall wellness and thus helping to reduce biological age. Mobile health (mHealth) interventions require numerous decisions that integrate behavioral theory, user feedback, and technical and practical feasibility considerations. The main purpose of this research program is to test if the application works as intended. This pilot study program is managed internally by Pepsico clinical researchers.

Being tested
Nutrition, Fitness, Sleep
Keywords
Biological age, Wellness app
Medical subject headings
Behavior

What participants receive

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

  • NutritionOther

    Interact with mobile app and work toward personalized nutrition goals

  • FitnessOther

    Interact with mobile app and work toward personalized fitness goals

  • SleepOther

    Interact with mobile app and work toward personalized sleep goals

Study groups in NCT06191822
Study groupRoleWhat they receive
NutritionOtherSet personalized nutrition goals
Receives: Other: Nutrition
FitnessOtherSet personalized fitness goals
Receives: Other: Fitness
SleepOtherSet personalized sleep goals
Receives: Other: Sleep

What is being measured

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

  1. Assess the technical characteristics of the app (App proficiency) -Connection

    Does the app work as intended: Ability to connect wearable devices

    Measured: Continuous for up to 6 weeks

  2. Assess the technical characteristics of the app (App proficiency) -Face scan age

    Does the app work as intended: Ability to conduct face scan to provide biological age

    Measured: Continuous for up to 6 weeks

  3. Assess the technical characteristics of the app (App proficiency) -Face scan stress

    Does the app work as intended: Ability to conduct face scan to provide stress index

    Measured: Continuous for up to 6 weeks

  4. Assess the technical characteristics of the app (App proficiency) -Face scan heart rate

    Does the app work as intended: Ability to conduct face scan to provide heart rate

    Measured: Continuous for up to 6 weeks

  5. Assess the technical characteristics of the app (App proficiency) -Onboarding

    Does the app work as intended: Onboarding sequence

    Measured: Continuous for up to 6 weeks

  6. Assess the technical characteristics of the app (App proficiency) -Goal selection

    Does the app work as intended: Ability to enter own goal

    Measured: Continuous for up to 6 weeks

  7. Assess the technical characteristics of the app (App proficiency) -Goal progress

    Does the app work as intended: Ability to track and measure goal progress (e.g., steps from a wearable device)

    Measured: Continuous for up to 6 weeks

  8. Assess the technical characteristics of the app (App proficiency) -Points assigned

    Does the app work as intended: Do points earned reflect what was completed in the app?

    Measured: Continuous for up to 6 weeks

  9. Assess the technical characteristics of the app (App proficiency) -Wellness scoring

    Does the app work as intended: Does wellness score change with lifestyle changes as intended? An improved wellness score is better.

    Measured: Continuous for up to 6 weeks

Secondary outcomes (5)
  1. Learnings to inform future versions of the app -Retention

    Exploratory analyses of the data aimed to help to inform clinical trial retention rates

    Measured: Continuous for up to 6 weeks

  2. Learnings to Inform future versions of the app -Overall engagement

    Exploratory analyses of the data aimed to help to inform predictors of engagement

    Measured: Continuous for up to 6 weeks

  3. Learnings to inform changes to future versions of the app -Specific engagement

    Exploratory analyses of the data aimed at informing engagement with specific app features

    Measured: Continuous for up to 6 weeks

  4. Learnings to inform changes to future versions of the app - Dietary behaviors

    Exploratory analyses of the data aimed at informing improvements in self-reported diet behaviors

    Measured: Continuous for up to 6 weeks

  5. Learnings to inform changes to future versions of the app -Lifestyle behaviors

    Exploratory analyses of the data aimed at informing improvements in self-reported lifestyle behaviors

    Measured: Continuous for up to 6 weeks

Timeline

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

  1. First posted5 Jan 2024
  2. Study start1 Mar 2022
  3. Primary completion1 Sep 2023
  4. Study completion1 Sep 2023

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
Other
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
1,714 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06191822
Sponsor's protocol ID
PEP- 2111/19 - 2302/07/08/09
Status last verified
Jun 2026
First submitted
13 Sep 2023
Last updated
5 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Nutrition, Fitness and Sleep in people with App Proficiency and Behavior, run by PepsiCo Global R&D 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 2 inclusion and 1 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 5 Jun 2026. 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?

Assess the technical characteristics of the app (App proficiency) -Connection (time frame: Continuous for up to 6 weeks). The study lists 9 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 5 Jun 2026; AzTrials last refreshed its copy on 27 Oct 2026.

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