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Clinical Trials/NCT01939860
NCT01939860
Completed
Not Applicable

A Feasibility Study of the Impact on Blood Pressure Control of Supplementing Community Pharmacist Services With Structured Information on Blood Pressure and Its Treatment

University of Warwick1 site in 1 country56 target enrollmentJanuary 2014
ConditionsHypertension

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
University of Warwick
Enrollment
56
Locations
1
Primary Endpoint
Changes in systolic or diastolic blood pressure
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Hypertension is a major health problem, however its control is unsatisfactory. One of the reasons for such a high prevalence of this disease includes poor patient compliance to treatment. Approximately 30 % of newly diagnosed hypertensive patients stop taking their blood pressure medication by six months and 50% by 12 months.

The UK government is keen to encourage community pharmacists to play an active role in participation of services that can improve patient adherence to their medications. The New Medicines Service (NMS) and targeted Medicines Use Reviews (MUR) are established services which fund community pharmacists to review and explain medicine use to patients, with hypertension a common condition for which advice is given within these schemes. Within these schemes, advice is verbal and unstructured, with no specific written information provided on drugs or the disease being treated.

This study aims to determine whether structured information provided to participants verbally and in writing by community pharmacists about blood pressure and current medicine(s) within NMS and targeted MURs will be retained and will be associated with improved hypertension control. Participants will be recruited from people eligible for NMS and MURs and attending community pharmacies.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
June 2014
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ejaz Cheema

PhD student

University of Warwick

Eligibility Criteria

Inclusion Criteria

  • 18 or over 2) male or female 3) Have been started on any blood pressure medication

Exclusion Criteria

  • Patients with English language problems

Outcomes

Primary Outcomes

Changes in systolic or diastolic blood pressure

Time Frame: 1 year (trial would be stopped at 26 weeks if it is not possible to recruit any further participants

Systolic and diastolic blood pressure will be measured and recorded in mm Hg using OMRON blood pressure monitors

Secondary Outcomes

  • change in the knowledge of hypertension(one year(trial would be stopped at 26 weeks if it is not possible to recruit any further participants))

Study Sites (1)

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