Web-based Support for People With Type 2 Diabetes
2 december 2015 uppdaterad av: University of Southampton
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.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Faktisk)
1041
Fas
- Inte tillämpbar
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
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
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Stödjande vård
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Trippel
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: 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
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
user engagement
Tidsram: This will be measured by intervention completion rates
|
This will be measured by intervention completion rates
|
Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Patient enablement
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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.
|
Andra resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Single item: whether you would recommend the website to others
Tidsram: 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.
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Utredare
- Huvudutredare: Lucy Yardley, University of Southampton
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 oktober 2014
Primärt slutförande (Faktisk)
1 september 2015
Avslutad studie (Faktisk)
1 november 2015
Studieregistreringsdatum
Först inskickad
21 mars 2013
Först inskickad som uppfyllde QC-kriterierna
23 april 2014
Första postat (Uppskatta)
24 april 2014
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
3 december 2015
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
2 december 2015
Senast verifierad
1 december 2015
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 4746
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .