JITAIs: Optimization of Effectiveness

Measuring, Analyzing and Mapping Environmental Influences on (and Changes in) Spatial Patterns: Evidence for Just-in-time Adaptive Interventions

The goal of this feasibility study is to get insight into the receptivity of a JITAI aimed at healthy dietary intake in inhabitants of a small city in the Netherlands.

The main question it aims to answer is:

• what is the right time and the right location to send notifications to people and for what type of interventions are people most receptive? Furthermore, the aim is to get insight into the relevance and usability of the app, the privacy concerns that people have and the perceived effectiveness of the app on dietary intake.

Participants will test our app for 2 weeks, of which they will receive prompts during one week.

Study Overview

• Status: Completed
• Conditions: Chronic Disease; Eating Behavior
• Intervention / Treatment: Device: Just-In-Time Adaptive Intervention

Detailed Description

JITAIs have already been developed in the fields of physical activity, smoking, alcohol use and mental illness. Within these fields, results were promising since JITAIs have proven to be effective in changing behaviour. Until now, no JITAIs have been developed that primarily focus on eating behaviour and it is expected that this type of interventions yields great potential in changing eating behaviour.

In this feasibility study a newly developed app is tested with the aim to get insight into what factors influence the receptiveness of people. Receptiveness is the person's ability to receive, process, and use the support provided, which is a prerequisite to achieve behaviour change. In the pilot study the aim is to investigate when and where the right time is to send notifications to people and for what type of interventions people are most receptive.

Participants are inhabitants of Wageningen who will test our app for 2 weeks. In the first week nothing is expected from the participants, but their movement patterns are collected via GPS; the participants are their own control for the Just-In-Time principle. In the second week the participants receive notifications (i.e., a healthy recipe, a tip for the healthier option at a certain location) based on their selected goal (eating more vegetables, eating less meat, less unhealthy snacking). After receiving the notification, participants are asked to answer several questions. At the end of the day, participants are asked to give us more insight in what they like and dislike to receive, at which locations, at what times, how many times a day, and their reasons behind this.

With this data the app can be further developed (co-creation).

The results of the study will be analysed within persons to visualize patterns. A second goal is to test if the movement patterns of participants can be used to objectively measure if interventions are effective in the future. The movement patterns will be analysed with the use of different algorithms, to see if and how movement patterns can say anything about the behaviour of people (stopping, standing still, alter routes). The movement patterns can be linked to received interventions, locations and receptivity.

Within this pilot study, people are not asked to alter their behaviour. Participants do receive notifications that are focused on making healthier eating choices, but the expectation is that this will not lead to behavioural changes within one week. The goal of the study is to get better insight into the best way to respond to the Just-In-Time principle. Participants will receive zero to several notifications a day for a period of 1 week.

• Study Type: Interventional
• Enrollment (Actual): 14
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Netherlands
  • Wageningen, Netherlands
    • Wageningen University and Research

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Open or motivated to improve their eating behaviour (as this is the target group of the final developed app)

  • Older than 18 years old
  • Living in Wageningen
  • Is able to understand and speak Dutch
  • Having an Android phone

Exclusion Criteria:

• Does not have a specific goal to improve eating behaviour

  • Is under 18 years old
  • Does not live in Wageningen
  • Does not speak and/or understand Dutch
  • Does not have an android phone

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Test group of app; All participants will first use the app one week without receiving just-in-time notifications. Their movement patterns are collected through GPS. In the second week, they will receive just-in-time notifications based on their chosen goal. Participants will act as their own control group.	Device: Just-In-Time Adaptive Intervention; Participants will be exposed to a new innovative app to test.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Receptivity	The receptiveness is measured with short questions after each prompt on whether the prompt is opportune. Questions on receptiveness are send after every prompt during one week (second week of the study). Dependent on how many locations people visit at which they receive a prompt.	Receptivity is measured during one week, after every prompt

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Movement patterns	Movement patterns are collected within the city of Wageningen using GPS.	Location is stored every 5 seconds during two weeks.

Collaborators and Investigators

• Sponsor: Wageningen University and Research
• Collaborators: ZonMw: The Netherlands Organisation for Health Research and Development

Study record dates

Study Major Dates

• Study Start (Actual): January 1, 2023
• Primary Completion (Actual): June 30, 2023
• Study Completion (Actual): June 30, 2023

Study Registration Dates

• First Submitted: January 12, 2023
• First Submitted That Met QC Criteria: March 6, 2023
• First Posted (Actual): March 17, 2023

Study Record Updates

• Last Update Posted (Estimated): December 13, 2023
• Last Update Submitted That Met QC Criteria: December 5, 2023
• Last Verified: December 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Disease Attributes; Chronic Disease
• Other Study ID Numbers: 555003027

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No