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Completed

NCT Number: NCT06191822

Aspire2B Personalization Pilot Study Program

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

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Remote, no facility visits. Managed by PepsiCo R&D Life Sciences

Chicago, Illinois, 60661, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Nutrition

Other

Interact with mobile app and work toward personalized nutrition goals

Fitness

Other

Interact with mobile app and work toward personalized fitness goals

Sleep

Other

Interact with mobile app and work toward personalized sleep goals

Primary outcomes

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

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

    Does the app work as intended: Onboarding sequence

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

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

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

Secondary outcomes

  1. Learnings to inform future versions of the app -Retention

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

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

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

    Time frame: Continuous for up to 6 weeks

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

Sponsors and collaborators

Lead sponsor

PepsiCo Global R&D

Industry

Registry information

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jan 5, 2024
Registry last updated
Jun 5, 2026

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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