- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05036382
Factors to Affect the Provision of Health Data of Users Through PHR App
A Study on Analysis of Factors to Affect the Provision of Health Data of Users Through the Personal Health Management Application
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Researchers send a weekly message to participants asking them to share their step data on their personal health records(PHR) applications. (4months in total)
(Baseline, 1month) For the first month, researchers send the same data request message to both counties.
- term, 1 month) The researchers added a message saying, 'Incentives are provided for data sharing' only to the experimental group.
- term, 1 month) Excludes incentive message for both groups
term, 1 month) The researchers added a message saying, 'Incentives are provided for data sharing' only to the control group.
- For equity in both groups, an incentive message was provided to the control group in the last month under the same conditions as the experimental group.
- Only the first 3 months of data were used for the study.
Hypothesis
- In 1-term, the number of data sharing in the experimental group is higher than that in the control group.
- In 1-term, the number of data sharing in the experimental group is more active than baseline period.
- In 2-term, the number of data sharing in the experimental group is still higher than in the baseline period.
- Over the next 1 month, the number of sharing in the experimental group was maintained, which was still higher than that of the control group.
Undersøgelsestype
Tilmelding (Forventet)
Kontakter og lokationer
Studiesteder
-
-
Bundang-gu, Seongnam-si
-
Gyeonggi-do, Bundang-gu, Seongnam-si, Korea, Republikken, 13620
- Seoul National University Bundang Hospital
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Adults aged 19 to 70
- A person who has no difficulty in installing and using PHR app under study
- A person who has expressed his/her willingness to participate voluntarily
Exclusion Criteria:
- Children/Adolescents under the age of 18 or Seniors over 71 years of age
- Those who do not have a smartphone or who are not proficient in using a smartphone
- Persons who are uncooperative and difficult to understand the research method due to cognitive decline
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Observationsmodeller: Case-Crossover
- Tidsperspektiver: Fremadrettet
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
---|---|
Experimental Group
A group that receives an incentive message one month after the start of the experiment
|
Sending more step data from the experimental group that received the incentive message
|
Control Group
A group that does not receive an incentive message (for equity, incentive messages will be sent in the last month of the experiment)
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Average number of data shares
Tidsramme: 3 months
|
The average number of steps data sharing between the experimental group and the control group according to the incentive message
|
3 months
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Percentage of participants with increased number of shares compared to baseline-term
Tidsramme: 3 months
|
3 months
|
Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Studer store datoer
Studiestart (Forventet)
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- clinical trials_1
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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