User Experience of a Mobile Application (SMart)

August 14, 2020 updated by: Danone Asia Pacific Holdings Pte, Ltd.

Evaluating the User Experience of a Mobile Application in Recording Primary Caregiver Reported Outcomes of Infants

To evaluate the user experience of the use of the different modules / trackers in the mobile application in recording primary caregiver reported outcomes of infants

Study Overview

Status

Terminated

Detailed Description

Using a questionnaire to collect overall user experience, frequency of usage, feedback of each module in the mobile application

Study Type

Observational

Enrollment (Actual)

6

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

      • Singapore, Singapore
        • KK Women's and Children's Hospital

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

No older than 1 year (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Infants from birth to ≤ 12 months of age and their primary caregiver

Description

Inclusion Criteria:

  1. Infants from birth to ≤ 12 months of age.
  2. Primary caregiver should have access to the internet and a smartphone or tablet to access the mobile application.
  3. Primary caregiver should be able to comprehend the content in the mobile application and complete the questionnaires in English.
  4. Primary caregiver takes care of the infant more than 50% of the time

Exclusion Criteria:

  • Incapability of the primary caregiver to access the mobile application using a smartphone or tablet with internet

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

Cohorts and Interventions

Group / Cohort
Primary Caregiver and infant pair
Primary Caregiver and infant who is less than or equal to 12 months old

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Overall User experience
Time Frame: Day 14
Using a questionnaire to assess primary caregiver reported overall experience on a 5-point scale (Very Poor to Very Good) of the mobile application
Day 14

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
User experience (ease of use) - Primary Caregiver
Time Frame: Day 14
Using a questionnaire to assess primary caregiver ease of use (Very Poor to Very Good or Did Not Use) of use of different modules/trackers in the mobile application
Day 14
User experience (frequency of use) - Primary Caregiver
Time Frame: Day 14
Using a questionnaire to assess primary caregiver frequency (Rarely to Always) of use of different modules/trackers in the mobile application
Day 14
User experience (usefulness) - Healthcare Professionals (HCP)
Time Frame: Day 14
Using a questionnaire to assess HCP reported usefulness (not useful at all to very useful) of the data generation by the mobile application
Day 14
User experience (relevance) - Healthcare Professionals (HCP)
Time Frame: Day 14
Using a questionnaire to assess HCP reported relevance (not relevant at all to very relevant) of the data generation by the mobile application
Day 14

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
User experience (ease of use) - Primary Caregiver from Day 0 to Day 45
Time Frame: Day 0 to Day 45
Using a questionnaire to assess primary caregiver reported user experience of different modules/trackers in the mobile application on a 5-point scale (Very Poor to Very Good) of the mobile application
Day 0 to Day 45
User experience (frequency of use) - Primary Caregiver from Day 0 to Day 45
Time Frame: Day 0 to Day 45
Using a questionnaire to assess primary caregiver reported user frequency of use of different modules/trackers in the mobile application on a 5-point scale (Rarely to Always) of the mobile application
Day 0 to Day 45
User experience (quality of insights) - Primary Caregiver from Day 0 to Day 45
Time Frame: Day 0 to Day 45
Using a questionnaire to collect quality of insights on a 5-point scale (Very Poor to Very Good) to describe primary caregiver reported events in the modules/trackers in the mobile application
Day 0 to Day 45
User experience (weighing scale) - Primary Caregiver from Day 0 to Day 45
Time Frame: Day 0 to Day 45
Using a questionnaire to assess primary caregiver user experience on a 5-point scale (Very Poor to Very Good) for the use of the weighing scale in measuring weight of their infants
Day 0 to Day 45
User feedback (weighing scale) - Primary Caregiver from Day 0 to Day 45
Time Frame: Day 0 to Day 45
Using an open-ended question to collect primary caregiver feedback for the use of the weighing scale in measuring weight of their infants
Day 0 to Day 45

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Poh Choo Khoo, MBBS, KK Women's and Children's Hospital

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)

December 26, 2019

Primary Completion (Actual)

June 26, 2020

Study Completion (Actual)

June 26, 2020

Study Registration Dates

First Submitted

December 6, 2019

First Submitted That Met QC Criteria

January 13, 2020

First Posted (Actual)

January 18, 2020

Study Record Updates

Last Update Posted (Actual)

August 18, 2020

Last Update Submitted That Met QC Criteria

August 14, 2020

Last Verified

August 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • EBB19GC27359

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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