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

NCT ID: NCT01939860

Last Updated: 2017-12-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

56 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-01-31

Study Completion Date

2014-06-30

Brief Summary

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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

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Conditions

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Hypertension

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Usual pharmacy care

Participants will not receive any structured written education on hypertension and its treatment

Group Type NO_INTERVENTION

No interventions assigned to this group

usual pharmacy care plus structured information

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.

Group Type EXPERIMENTAL

Written and verbal patient education on hypertension and its treatment

Intervention Type OTHER

Interventions

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Written and verbal patient education on hypertension and its treatment

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

1)Patients with English language problems
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Warwick

OTHER

Sponsor Role lead

Responsible Party

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Ejaz Cheema

PhD student

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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J P Goes chemist

Coventry, , United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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Warwick.123

Identifier Type: -

Identifier Source: org_study_id