- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04231188
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
Conditions
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:
- Infants from birth to ≤ 12 months of age.
- Primary caregiver should have access to the internet and a smartphone or tablet to access the mobile application.
- Primary caregiver should be able to comprehend the content in the mobile application and complete the questionnaires in English.
- 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.
Clinical Trials on User Experience of Mobile Application
-
Sevda DemirelGGZ CentraalCompletedWork-Related Stress | Coping Behaviour | User Experience of Mobile ApplicationNetherlands
-
University Hospital, AngersNot yet recruiting
-
University of ZurichUnknown
-
Vander Haegen MarieWithdrawn
-
Agri Ibrahim Cecen UniversityAtaturk UniversityCompleted
-
University Hospitals Cleveland Medical CenterCompleted
-
Ocon Medical Ltd.CompletedTo Assess the Safety, Effectiveness and User Experience of the Scu 300A IUBBulgaria, Romania
-
McGill UniversityMcGill University Health Centre/Research Institute of the McGill University...CompletedMedication Adherence | Mobile ApplicationCanada
-
Sinop UniversityRecruitingMobile Application | Knee ProsthesisTurkey
-
Ege UniversityNot yet recruitingOstomy | Mobile Application | Stoma