User Experience of a Mobile Application (SMart)
14. august 2020 opdateret af: 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
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
Using a questionnaire to collect overall user experience, frequency of usage, feedback of each module in the mobile application
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
6
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
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Singapore, Singapore
- KK Women's and Children's Hospital
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
Ikke ældre end 1 år (Barn)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Sandsynlighedsprøve
Studiebefolkning
Infants from birth to ≤ 12 months of age and their primary caregiver
Beskrivelse
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
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
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Primary Caregiver and infant pair
Primary Caregiver and infant who is less than or equal to 12 months old
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Overall User experience
Tidsramme: Day 14
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Using a questionnaire to assess primary caregiver reported overall experience on a 5-point scale (Very Poor to Very Good) of the mobile application
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Day 14
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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User experience (ease of use) - Primary Caregiver
Tidsramme: Day 14
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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
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Day 14
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User experience (frequency of use) - Primary Caregiver
Tidsramme: Day 14
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Using a questionnaire to assess primary caregiver frequency (Rarely to Always) of use of different modules/trackers in the mobile application
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Day 14
|
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User experience (usefulness) - Healthcare Professionals (HCP)
Tidsramme: Day 14
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Using a questionnaire to assess HCP reported usefulness (not useful at all to very useful) of the data generation by the mobile application
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Day 14
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User experience (relevance) - Healthcare Professionals (HCP)
Tidsramme: Day 14
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Using a questionnaire to assess HCP reported relevance (not relevant at all to very relevant) of the data generation by the mobile application
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Day 14
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Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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User experience (ease of use) - Primary Caregiver from Day 0 to Day 45
Tidsramme: Day 0 to Day 45
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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
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Day 0 to Day 45
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User experience (frequency of use) - Primary Caregiver from Day 0 to Day 45
Tidsramme: 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
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Day 0 to Day 45
|
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User experience (quality of insights) - Primary Caregiver from Day 0 to Day 45
Tidsramme: Day 0 to Day 45
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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
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Day 0 to Day 45
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User experience (weighing scale) - Primary Caregiver from Day 0 to Day 45
Tidsramme: Day 0 to Day 45
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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
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Day 0 to Day 45
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User feedback (weighing scale) - Primary Caregiver from Day 0 to Day 45
Tidsramme: Day 0 to Day 45
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Using an open-ended question to collect primary caregiver feedback for the use of the weighing scale in measuring weight of their infants
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Day 0 to Day 45
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Poh Choo Khoo, MBBS, KK Women's and Children's Hospital
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
26. december 2019
Primær færdiggørelse (Faktiske)
26. juni 2020
Studieafslutning (Faktiske)
26. juni 2020
Datoer for studieregistrering
Først indsendt
6. december 2019
Først indsendt, der opfyldte QC-kriterier
13. januar 2020
Først opslået (Faktiske)
18. januar 2020
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
18. august 2020
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
14. august 2020
Sidst verificeret
1. august 2020
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- EBB19GC27359
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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Ingen
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Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .