- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT00933855
Patient Communication Training Intervention
A Feasibility Study of a Patient Communication Training Intervention
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
It is well accepted that effective physician-patient communication is associated with important outcomes. Communication training interventions for oncologists and other clinicians has been shown to be effective in changing behavior and improving outcomes. Less attention has been given to improving cancer patients' communication with their physicians. Most of the studies in this area have been focused on activating patients through training them to ask questions. Although question asking is a vitally important patient communication skill, other patient communication skills should also be encouraged for patients.
In the primary care setting, studies on patient communication training have focused on three additional communication skills to asking questions: presenting information, checking understanding, and expressing concerns. The goal of this study is to pilot test a patient communication workshop that builds on the work done in the primary care setting, offering an intervention that focuses on a broad range of skills. The proposal aims to improve communication skills in an underserved population, which may be a factor contributing to minority health disparities.
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
-
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New York
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Jamaica, New York, États-Unis, 11432
- Queens Hospital Center
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- Patients seeing a physician at Queens Cancer Center (not family members or partners)
- Able to provide informed consent.
Exclusion Criteria:
- Less than 18 years of age (as per self-report)
- Cognitive or physical impairment rendering patients incapable of providing informed consent to participate in the study.
- As the workshop will be given in English and the measures are all written in English, subjects who are not fluent in English will be excluded.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
|
communication training workshop
The patient intervention is a 1 hour communication workshop entitled: "Getting the Most out of your Doctor's Visit."
The workshops will be offered to both patients and family members, but data will be collected only for patients.
The workshops will be held on location at Queens Cancer Center.
|
We will recruit a minimum of 1 and maximum of 12 patients for each workshop. The workshop will follow the approximate time table below: 10 minutes: Sign-in, welcome and introductions 25 minutes: Didactic session, videos and discussion 10 minutes: Group discussion 15 minutes: Closing plenary and final assessment |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
To determine the feasibility of a patient communication training intervention.
Délai: 2 years
|
2 years
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
To attain preliminary data on the acceptability of the intervention through patient ratings of effectiveness and usefulness of the intervention.
Délai: 2 years
|
2 years
|
|
To attain preliminary data on the effect of a patient communication training intervention on patients' self-reported communication behaviors.
Délai: 2 years
|
2 years
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Carma Bylund-Lincoln, PhD, Memorial Sloan Kettering Cancer Center
Publications et liens utiles
Liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- 08-148
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .