- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02122250
Web-based Support for People With Type 2 Diabetes
Developing and Testing Accessible Web-based Support for Patient Self-management of Diabetes
This project will address vital questions regarding how best to design web-based materials for the growing population of patients with basic literacy and computer skills but lower levels of health literacy, building on our previous experience of developing web-based materials for people with lower levels of literacy and health literacy.
This study will be carried out two phases. Phase 1 will use qualitative methods to understand user experiences of the web-based materials through observational 'think-aloud' interviews with users. Phase 2 will test the newly developed web-based materials to a static (non-interactive) version of the materials online.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Potential participants are patients with Type 2 diabetes aged 18 years or more, who are able to consent.
Exclusion Criteria:
- Severe mental health problems, palliative care, recent bereavement, known opposition to involvement in research or inability to complete research measures, e.g. learning disability, inability to read / speak English.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Støttende omsorg
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Trippel
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Eksperimentell: Interactive web-based materials
Interactive web-based materials for self-management of diabetes
|
Interactive web-based materials for self-management of diabetes
|
Aktiv komparator: Static web-based materials
Static version of the interactive web-based materials
|
Static web-based materials
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
user engagement
Tidsramme: This will be measured by intervention completion rates
|
This will be measured by intervention completion rates
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Patient enablement
Tidsramme: Participants will be followed up as soon as they finished looking at the website, which is expected to be 20-40 minutes after they start the study.
|
Participants will be followed up as soon as they finished looking at the website, which is expected to be 20-40 minutes after they start the study.
|
Website satisfaction
Tidsramme: Participants will be followed up as soon as they finished looking at the website, which is expected to be 20-40 minutes after they start the study.
|
Participants will be followed up as soon as they finished looking at the website, which is expected to be 20-40 minutes after they start the study.
|
Physical activity attitudes and intentions
Tidsramme: Participants will be followed up as soon as they finished looking at the website, which is expected to be 20-40 minutes after they start the study.
|
Participants will be followed up as soon as they finished looking at the website, which is expected to be 20-40 minutes after they start the study.
|
Diabetes and Physical activity knowledge
Tidsramme: Participants will be followed up as soon as they finished looking at the website, which is expected to be 20-40 minutes after they start the study.
|
Participants will be followed up as soon as they finished looking at the website, which is expected to be 20-40 minutes after they start the study.
|
Andre resultatmål
Resultatmål |
Tidsramme |
---|---|
Single item: whether you would recommend the website to others
Tidsramme: Participants will be followed up as soon as they finished looking at the website, which is expected to be 20-40 minutes after they start the study.
|
Participants will be followed up as soon as they finished looking at the website, which is expected to be 20-40 minutes after they start the study.
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Lucy Yardley, University of Southampton
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 4746
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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