- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01131715
Pharmacist Follow-up, a Qualitative Study of Patient Experience
June 25, 2020 updated by: Beate Hennie Garcia, PhD, Hospital Pharmacy of North Norway Trust
Pharmacist Follow-up of Patients With Coronary Heart Disease. A Qualitative Study of Patient Experience.
A pharmacist follow-up procedure is under development.
Patients with coronary heart disease (CHD) is being followed up by a pharmacist for one year with three meetings; at discharge from hospital, after three months and after one year.
The evaluation is basically based on quantitative measures as achievement of therapeutic goals, number of drug related problems detected, hospitalisations etc.
However, the patients' own experience with the follow-up procedure cannot be evaluated using these measures.
Thus, a qualitative approach is needed.
In this study, a total of four patients participating in the follow-up will be included and interviewed.
A semistructured interview guide will be used.
Interviews will be taped, transcribed and analyzed with the intention to explore how patients experience the follow-up from the pharmacist.
A thoruough content analysis will be performed.
Patients included must have met the pharmacist at least twice.
The pharmacist in charge of the follow-up will recruit patients and hand out study information.
Patients will reply to the principal investigator of the study and thus kept anonymous for the pharmacist in charge of the follow-up.
No pressure will be put on the patients to join, but it will be emphasized that it will help evaluating the procedure.
Study Overview
Status
Completed
Conditions
Detailed Description
See full publication on http://www.biomedcentral.com/1756-0500/7/197
Garcia et al.
BMC Research Notes 2014, 7:197
Study Type
Observational
Enrollment (Actual)
4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Tromso, Norway, 9037
- University of Tromsoe
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients included in the study "Pharmacist follow-up of patients with CHD".
Description
Inclusion Criteria:
- must have met the pharmacist at least twice
- living within the area of Tromsoe city so that interviews are possible
Exclusion Criteria
- none as patients are already enrolled in another study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Study group
Patients who are included in the pharmacist follow-up procedure
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Qualitative evaluation of the impact of pharmacist follow-up via interviews with the participating patients
Time Frame: 3 months or 1 year
|
In the pharmacist follow-up procedure under development, patients have individual "consultations" with a pharmacist three times.
Patients are recruited to this study at the second or third consultation.
Interviews will be performed with patients included to explore how patients' experience this follow-up procedure.
Outcome measures from patient interviews can be counted.
In qualitative research, the content of the interviews are thoroughly analysed with focus on the meaning of the informant's/interviewee's sayings.
Outcomes will be presented as overall themes touched by the informants.
|
3 months or 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Lars Smaabrekke, PhD, University of Tromso
- Study Chair: Beate H Garcia, PhD, Hospital Pharmacy of North Norway Trust
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2010
Primary Completion (Actual)
March 1, 2010
Study Completion (Actual)
July 1, 2012
Study Registration Dates
First Submitted
April 30, 2010
First Submitted That Met QC Criteria
May 26, 2010
First Posted (Estimate)
May 27, 2010
Study Record Updates
Last Update Posted (Actual)
June 29, 2020
Last Update Submitted That Met QC Criteria
June 25, 2020
Last Verified
June 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SHAN-002
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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