- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00182325
Effects of a Personalized Web-based Antenatal Care Planner
Women's Web Access to Their Own Antenatal Health Record and Personalized Health Information: Effect on Pregnancy Health Outcomes and Patient Satisfaction
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Many women are turning to the Internet to meet their health information needs, but the large amount of information available, as well as the unknown reliability and applicability of information can be overwhelming. Studies in specific patient populations have determined that patients given access to personalized, on-line medical information are more satisfied with their care than patients provided generalized information. None of these studies have looked at whether this type of patient education would be helpful for pregnant women. This study is being done to determine whether pregnant women who have access to their own health records and personalized health information over the Internet are more satisfied with their prenatal care, and if they are more compliant with health visits and tests, compared to pregnant women who receive only generic pregnancy information on the Internet and from pamphlets
Women are being randomly assigned to receive secure access to pregnancy health information links chosen by the centre's physicians, or to receive these links with access to their online personal health that includes the antenatal record and a section of their care planner, from the centre's electronic medical record
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
-
-
Ontario
-
Hamilton, Ontario, Canada, L8N 3Z5
- McMaster University
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- less than 28 weeks pregnant access to Internet
Exclusion Criteria:
- cannot speak/read English and no translator
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Altro
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: personalized web prenatal information
Personalized health information for pregnancy through personal health record
|
|
|
Comparatore attivo: general web prenatal information
General pregnancy health related websites
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Uptake of Service
Lasso di tempo: 11 months
|
Number of log-ins
|
11 months
|
|
Easy to Log on
Lasso di tempo: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Information Easy to Understand
Lasso di tempo: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Learned Something New
Lasso di tempo: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Easy to Find Information
Lasso di tempo: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Helped me Stay Healthy
Lasso di tempo: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Helped me Learn About Risks
Lasso di tempo: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Helped me Understand Tests
Lasso di tempo: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Helped me Make Decisions
Lasso di tempo: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Helped me Remember Appointments
Lasso di tempo: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
Collaboratori e investigatori
Collaboratori
Investigatori
- Investigatore principale: Heather Waters, MD, McMaster University
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Altri numeri di identificazione dello studio
- RDF-160
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .