- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT03829995
Effect of Pharmacist Provided Drug Information Services After Hospital Discharge
Effect of Pharmacist Provided Drug Information Services After Hospital Discharge: Patient Satisfaction and Sense Of Security Regarding Drug Treatment.
Objective:
The aim of this study is to evaluate if offering drug counseling from a hospital pharmacy increases patient satisfaction and sense of security regarding drug treatment after hospital discharge.
Aperçu de l'étude
Description détaillée
Method and design:
This study was estimated to include 250 participants in a clinical randomized controlled trial. The participants were included from the Acute Medical Ward and the Department of Respiratory Medicine at Bispebjerg Hospital when discharged. The participants were randomized to one of two groups with unequal sizes: the control (50 participants) or intervention group (200 participants). This study used blocked randomization with block sizes of 5/10/15/20/25. The control group received the normal care following the Danish standard procedure. Participants in the intervention group also received the normal care but was also offered the possibility to contact a hospital pharmacy department by phone or mail and ask questions regarding drug-related issues.
Data for the primary outcome measures was collected 14 days after discharge through structured phone interviews. An interview guide with a semi-structured questionnaire and already validated questions were developed, pre-tested and optimized. The participants were asked to answer open-ended questions, closed-ended question and rate statements or questions on a five-point scale.
The participants in the control group were asked to answer 13 items (seven questions or statements on a five-point scale, four closed-ended questions and two open-ended questions).
The participants in the intervention group who did not make any queries were asked the same questions as the participants in the control group and additionally three closed-ended questions. A total of 16 items.
The participants in the intervention group who made queries were asked the same questions as the participants in the intervention group who did not make any queries and additionally five questions on a five-point scale, four closed-ended and one open-ended question. A total of 27 items.
The effect of the drug counseling regarding patient safety was evaluated by a pharmaceutical assessment in which it was assessed whether the drug counseling had potentially prevented a drug-related problem.
Quantitative data from the phone interviews will be analyzed in Microsoft excel with descriptive statistics and simple parametric statistics. An analysis will determine whether there is a difference in the primary outcome measures.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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København NV
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Copenhagen, København NV, Danemark, 2400
- Capital Regions Hospital Pharmacy
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Patients discharged from the acute medical ward and department of respiratory medicine at Bispebjerg Hospital.
- Patients discharged to own home.
- Can speak the danish language.
- ≥18 years old.
- Can be contacted by phone.
Exclusion Criteria:
- Cognitive and communicative problems (e.g. dementia, aphasia, suicidal) or other barriers that unable the participant to use the intervention service.
- Patient does not answer phone within five attempts on five different days, when trying to conduct patient interview.
- Cognitive and communicative problems that unable the participant to answer questions in the patient interview.
- Deceased or readmitted before patient interview.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Recherche sur les services de santé
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Aucune intervention: Control group
Participants in the control group received the normal care following the Danish standard procedure.
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Comparateur actif: Intervention group
Participants in the intervention group received the normal care following the Danish stadard procedure.
Additionally the participants was also offered the possibility to contact a hospital pharmacy department by phone or mail for drug counseling.
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Participants can contact a hospital pharmacy department by phone or mail and ask questions regarding drug-related issues.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Sense of security regarding drug treatment and satisfaction with drug counseling.
Délai: 2-4 weeks after discharge.
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The questionnaire comprised closed-ended questions, open-ended questions and questions or statements where the respondents were asked to rate the questions or statements on a five-point scale.
The scale used is a attitude measurement scale that assess attitudes by presenting respondents with sentences that state beliefs about the particular attitude being measured.
The respondents then decide to what extent he or she agrees with the statement.
The responses are divided numerically into a series of ordered responses.
Ratings: 1 = not at all, 2 = to a small extent, 3 = to some extent, 4 = to a great extent, 5 = to a very great extent.
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2-4 weeks after discharge.
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Number of medications by admission.
Délai: Within one week after discharge.
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Number of medications will be read in admission report.
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Within one week after discharge.
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Number of medications by discharge.
Délai: Within one week after discharge.
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Number of medications will be read in discharge report..
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Within one week after discharge.
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Number of patients that received medication review by pharmacist during admission.
Délai: Within one week after discharge.
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The patient's journal will be searched for a medication review.
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Within one week after discharge.
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Number of patients that received help with medication at home after discharge.
Délai: Within one week after discharge.
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The patient's journal will be searched for information regarding help with medication at home.
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Within one week after discharge.
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Number of enquiries.
Délai: Directly after the patient received drug counseling.
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Patient enquiries will be classified to one of the predefined categories: adverse effects, choice of therapy, dosage and administration, interactions, product information, storage and handling, indication or other.
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Directly after the patient received drug counseling.
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Number of potentially prevented drug-related problems.
Délai: Directly after the patient received drug counseling.
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The pharmacist that performed the drug counseling assessed whether the drug counseling had potentially prevented a drug-related problem.
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Directly after the patient received drug counseling.
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Cause of hospitalization.
Délai: Within one week after discharge.
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The patient's journal will be searched for cause of hospitalization.
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Within one week after discharge.
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Tim E Vejborg, M.Sc.Pharm, Region Hovedstadens Apotek
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
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 (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
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
- H-18003889
Informations sur les médicaments et les dispositifs, documents d'étude
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