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

Not Applicable

Completed

• Conditions: Hypertension
• Interventions: Other: Written and verbal patient education on hypertension and its treatment

• Registration Number: NCT01939860
• Lead Sponsor: University of Warwick

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.

Detailed Description

Not available

Basic Information
|
Recruitment & Eligibility
|
Study & Design
|
Trial Locations

Study Timeline

• Study First Submitted: 2013-09-03
• Study First Submitted QC: 2013-09-05
• Study First Posted: 2013-09-11
• Study Start: 2014-01
• Primary Completion: 2014-06
• Study Completion: 2014-06
• Status Verified: 2017-12
• Last Update Submitted: 2017-12-04
• Last Update Posted: 2017-12-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 56

Inclusion Criteria

1)18 or over 2) male or female 3) Have been started on any blood pressure medication

Read More

Exclusion Criteria

1)Patients with English language problems

Read More

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
usual pharmacy care plus structured information	Written and verbal patient education on hypertension and its treatment	Participants will be provided with validated verbal and written information on hypertension and its treatment, including information about class (es) of anti-hypertensive medication(s) used by each patient, and their common side-effects. The written material will be based on validated patient information leaflets from the British Heart Foundation and the Blood Pressure Association.

Primary Outcome Measures

Name	Time	Method
Changes in systolic or diastolic blood pressure	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 Outcome Measures

Name	Time	Method
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)

Trial Locations

Locations (1)

J P Goes chemist; 🇬🇧 Coventry, United Kingdom