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CompletedNCT01101737Updated Apr 12, 2010

Trial of a Nurse Led Hypertension Clinic in Inner City General Practices

An interventional study of Nurse-led blood pressure clinic in Hypertension, sponsored by St George's, University of London. Completed at 1 site in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2010-04-12.

Sponsored by St George's, University of London · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
353
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The investigators will do a trial in two general practices to see if the introduction of a blood pressure clinic staffed by a specialist nurse supported by visiting consultant improves blood pressure control compared to usual care.

02

Conditions studied

  • Hypertension

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Keywords

  • Hypertension, clinical trial, nurse-led clinic, primary care
03

In context

Hypertension

6,689 studies on the registry are indexed under Hypertension; 965 are open to participants now.

This study's enrollment of 353 is above the median of 90 across 4,995 interventional studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

St George's, University of London is the lead sponsor of 105 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Patients with last recorded blood pressure greater or equal to the British Hypertension Society audit standard

Exclusion criteria

Exclusion Criteria:

  • Secondary hypertension
  • Housebound
  • Non-English speaking
  • Another major illness likely to dominate pattern of care e.g. advanced cancer, dementia
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
353 participants (actual)

Study arms

  • No intervention
    Usual care

    Patients not invited to the nurse-led clinic will continue with usual GP care

  • Experimental
    Nurse-led blood pressure clinic

    Patients randomly allocated to the intervention will be invited to a specialist nurse-led blood pressure clinic.

    Other: Nurse-led blood pressure clinic

Interventions

  • OtherNurse-led blood pressure clinic

    Blood pressure will be measured according to protocol.For patients with blood pressure above optimal targets, treatment changes will be discussed with the patient, a visiting consultant physician and the patient's GP. If they agree, the GP will intensify anti-hypertensive treatment with monthly follow up by the specialist nurse until BP targets are achieved.

06

What researchers measure

Primary outcomes

  1. Change in systolic blood pressure

    This will be assessed using two audits of practice records where blood pressure was measured and recorded independently by practice staff

    Time frame: 6 months

Secondary outcomes

  1. Proportion of patients in each group with final blood pressure below the British Hypertension Society optimal target

    Time frame: 6 months after recruitment

07

Study locations

1 site
  • St George's, University of London
    London, SW17 ORE, United Kingdom
08

References and documents

Publications

  • Dean SC, Kerry SM, Khong TK, Kerry SR, Oakeshott P. Evaluation of a specialist nurse-led hypertension clinic with consultant backup in two inner city general practices: randomized controlled trial. Fam Pract. 2014 Apr;31(2):172-9. doi: 10.1093/fampra/cmt074. Epub 2013 Dec 19. PubMed 24356073 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 12, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01101737
Lead sponsor
St George's, University of London
First posted
Apr 12, 2010
Start date
Feb 2008
Primary completion
Dec 2009
Completion
Apr 2010
Last update
Apr 12, 2010

Study contacts

Sally Dean, SRN
principal investigator · St George's, University of London
Pippa Oakeshott, MD
study director · St George's, University of London

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2010. You cannot join it, but the record below documents what was studied.

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