A Relational Artificial Intelligence (AI) Chatbot for App-Based Physical Activity Promotion

September 9, 2023 updated by: University of California, Davis

A Relational Artificial Intelligence (AI) Chatbot for App-Based Physical Activity Promotion Intervention Among Adults With a Sedentary Lifestyle

This study aims to empirically test the theoretical mechanisms of relational perceptions in the context of building and testing a relational artificial intelligence (AI) chatbot for improving physical activity (PA) behaviors among a sedentary adult population in the U.S.

The aim of the study is to build and experimentally test relational capacities of AI chatbot in inducing positive human-AI relationship and leading to higher PA behavior change intention. During the 7-day intervention, the relational chatbot will educate participants on physical activity using 5 types of relational messages during a PA intervention including 1) social dialogue, 2) empathy, 3) self-disclosure, 4) meta-relational communication, and 5) humor. On the other hand, the non-relational chatbot will only deliver PA intervention messages, without relational cues. Relational chatbot condition will be compared to the non-relational chatbot condition to assess its effectiveness.

The objective of this study is to test the efficacy of the mobile app intervention leveraging chatbots in increasing participants' relationship perception and physical activity behavior change.

Study Overview

Detailed Description

Despite the recognition of the importance of communication for relationship and trust building in healthcare programs (Ward, 2018), theoretical work and empirical testing of relational capacities in AI chatbot designed for changing health behaviors is lacking in previous research. In our systematic review of AI chatbot-based interventions on PA, diet, and weight loss outcomes, it was found that although majority of studies programmed AI chatbots to engage in relational communication behaviors (e.g., personalized greetings, showing empathy and compassion), none of these studies tested whether AI chatbot's relational capacities contributed to human-AI trust and relationship building (Oh et al., 2021). Beyond knowing some chatbots were perceived to be useful and friendly, we do not know theoretical mechanisms for what relational conversational strategies contribute to higher quality relationship perception and behavior outcomes.

By developing an AI chatbot that provides access to informational, motivational, and socio-emotional aspects of care will open new opportunities for delivering accessible interventions to improve sedentary population's PA behaviors. More broadly, the test of the AI Chatbot Behavior Change Model (Zhang et al., 2020) will provide the first empirical evidence on the model's utility and working mechanisms accounting for how relational AI chatbot can change health behaviors. If successful, the theoretical model and design of the relational chatbot will be able to generalize to related behavior change fields.

This field experiment will randomly assign participants to relational chatbot condition or non-relational (control) chatbot condition. Both conditions will involve an information component addressing physical activity education sessions.

The objective of this study is to test the efficacy of the mobile app intervention leveraging chatbots in increasing participants' relationship perception and physical activity behavior change.

Study Type

Interventional

Enrollment (Estimated)

140

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Davis, California, United States, 95616
        • University of California, Davis

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Living in the United States
  • Adults (18 years or older)
  • Able to speak and read English
  • Physically inactive at work and/or during leisure time
  • Having internet access to use the chatbot
  • Smartphone users

Exclusion Criteria:

  • Adults unable to consent
  • Individuals who are not yet adults (infants, children, teenagers)
  • Prisoners
  • Pregnant women
  • Physically active individuals who are meeting physical activity guidelines
  • Individuals who have participated in a physical activity intervention in the past 12 months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Non-Relational Chatbot Physical Activity Intervention
Participants are randomly assigned to a non-relational chatbot in a mobile app. The chatbot will provide physical activity education sessions. The chatbot will not engage in relational conversation behaviors.
Mobile app-based intervention. Participants will engage in a daily chat with a physical activity promotion chatbot. The chatbot does not, or only minimally, provide relational behavioral cues. Participants will view their progress of daily step counts.
Experimental: Relational Chatbot Physical Activity Intervention
Participants are randomly assigned to a relational chatbot in a mobile app. The chatbot will provide physical activity education sessions. The chatbot will engage in relational conversation behaviors.
Mobile app-based intervention. Participants will engage in a daily chat with a physical activity promotion chatbot. The chatbot provides relational behavioral cues. Participants will view their progress of daily step counts.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Relationship perception
Time Frame: 1 week
12-item measure based on Therapeutic Alliance Scale as an indication of relationship between participants and the chatbot. Ranges from 1 = "strongly disagree" to 5 = "strongly agree."
1 week
Changes in physical activity behavior
Time Frame: Baseline and 1 week
6-item measure based on 2008 Physical Activity Guidelines for Americans. Record the types of physical activities, days, and minutes.
Baseline and 1 week
Physical activity behavior (step counts)
Time Frame: Daily, 1 week
Step counts across 7 days (1 week) of intervention.
Daily, 1 week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Chatbot usability
Time Frame: 1 week
13-item measure of usability of the chatbot based on chatbot usability questionnaire (CUQ). Ranges from 1 = "strongly disagree" to 5 = "strongly agree."
1 week
Chatbot perception
Time Frame: 1 week
17-item measure of the perceived warmth and competence of the chatbot. Ranges from 1 = "strongly disagree" to 5 = "strongly agree."
1 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 5, 2023

Primary Completion (Estimated)

October 1, 2024

Study Completion (Estimated)

December 1, 2024

Study Registration Dates

First Submitted

March 20, 2023

First Submitted That Met QC Criteria

March 20, 2023

First Posted (Actual)

April 3, 2023

Study Record Updates

Last Update Posted (Actual)

September 13, 2023

Last Update Submitted That Met QC Criteria

September 9, 2023

Last Verified

September 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2033031

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared with other researchers.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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