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Understanding and Appraising the New Medicine Service in England (NMS)

Primary Purpose

Asthma, Pulmonary Disease, Chronic Obstructive, Diabetes Mellitus, Type 2

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
New Medicine Service
Sponsored by
University of Nottingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Asthma

Eligibility Criteria

14 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Community dwelling patients eligible for NMS (aged from 14 years starting a new medicine for asthma/COPD, diabetes (Type 2), antiplatelet/anticoagulation or hypertension).

Exclusion Criteria:

  • Patients collecting a repeat prescription for a medicine (i.e. not new) for asthma/COPD, type 2 diabetes mellitus (T2DM), antiplatelets/anticoagulants or hypertension
  • Patients collecting a medicine where the only change from the previous medicine involves a dosage or formulation change only
  • Participants who are unable to understand patient/participant study documents
  • Participants who are unable and unwilling to provide written consent / assent

Sites / Locations

  • Nottinghamshire County PCT/ County Health Partnerships
  • Doncaster PCT
  • Cambden, Barnet, Islington PCTs
  • Nottingham City PCT/Nottingham City Care

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

NMS

Current Practice

Arm Description

Patients in this arm will receive the full NMS service

Patients in this arm will receive the normal advice with their new medicine as dictated by current professional practice

Outcomes

Primary Outcome Measures

Medicines adherence
Patients will report medicines adherence using the service specified adherence question and against standard adherence scales
Cost effectiveness
Patients will record all NHS resource use during the study period via a self completion diary to assess the impact on cost effectiveness up to 6 months post initiation.
Operation of the NMS
The investigators will qualitatively describe the operation of the NMS, the complexity and nature of resulting consultations in terms of patient engagement, advice-giving and support. Additionally it will determine acceptability to stakeholders, reasons for success or lack of success, feasibility within the service delivery environment and generalisability and replicability across disease indications and community pharmacy settings

Secondary Outcome Measures

Patients' understanding of their medicines
The investigators will qualitatively evaluate patients' understanding of their medicines and the extent to which they are informed and supported in their medicines-related behaviour.
Pharmacovigilance
The investigators will qualitatively determine whether NMS encourages improved pharmacovigilance by community pharmacists and patients.
Stakeholder experience
The investigators will qualitatively characterise patient (and/or carer) and professional experience.
Professional relationships
The investigators will qualitatively explore inter-professional and patient-professional relationships.

Full Information

First Posted
June 19, 2012
Last Updated
May 27, 2015
Sponsor
University of Nottingham
Collaborators
Department of Health, United Kingdom, University College, London, University of Warwick
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1. Study Identification

Unique Protocol Identification Number
NCT01635361
Brief Title
Understanding and Appraising the New Medicine Service in England
Acronym
NMS
Official Title
Understanding and Appraising the New Medicine Service in England
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Completed
Study Start Date
August 2012 (undefined)
Primary Completion Date
April 2014 (Actual)
Study Completion Date
April 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nottingham
Collaborators
Department of Health, United Kingdom, University College, London, University of Warwick

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
About 25% medicines prescribed for long term conditions are not taken as directed, and approximately 15% people receiving a new medicine take few, if any, doses. The New Medicine Service (NMS) is a community pharmacy service that started in England in October 2011 which involves the pharmacist providing additional support to patients starting a new medicine for some breathing problems (asthma & COPD), high blood pressure, adult onset diabetes or medicines which reduce blood clotting. It aims to improve the way patients take their medicines improving outcomes and reducing costs to the National Health Service (NHS). The investigators will assess the effectiveness and cost effectiveness of the NMS using a research study where some people will receive the NMS, and some won't, so The investigators can look at the effect of the NMS on problems with their medicines, medicines taking and use of the NHS in general. Data will be collected in the East Midlands, South Yorkshire and London areas. The investigators will recruit 500 patients from a range of different pharmacies and follow them up at six, ten and twenty six weeks after starting their new medicine to assess effects on medicines taking behaviour, patients' reported problems with medicines, referrals to their General Practitioner (GP) and use of NHS resources. The investigators will compare the data gathered from this study with that being collected routinely by all pharmacies in England to provide wider estimates of cost effectiveness. The investigators will also explore how the NMS service is being implemented by pharmacies. A sample of patients from the main study will be followed in more detail. This will involve recording the consultations with the pharmacist and also interviewing patients about their experience of the service. The investigators will interview the patients GP to investigate their views of the service. The investigators will also try to understand why people decline the invitation for the NMS

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma, Pulmonary Disease, Chronic Obstructive, Diabetes Mellitus, Type 2, Hypertension, Blood Coagulation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
504 (Actual)

8. Arms, Groups, and Interventions

Arm Title
NMS
Arm Type
Experimental
Arm Description
Patients in this arm will receive the full NMS service
Arm Title
Current Practice
Arm Type
No Intervention
Arm Description
Patients in this arm will receive the normal advice with their new medicine as dictated by current professional practice
Intervention Type
Other
Intervention Name(s)
New Medicine Service
Intervention Description
The New Medicine Service is an intervention where patients prescribed a new medicine receive followup consultations with the pharmacist 7-14 days and 14-21 days after receiving the new prescription item
Primary Outcome Measure Information:
Title
Medicines adherence
Description
Patients will report medicines adherence using the service specified adherence question and against standard adherence scales
Time Frame
Change in adherence from 6 weeks to 10 weeks and 26 weeks
Title
Cost effectiveness
Description
Patients will record all NHS resource use during the study period via a self completion diary to assess the impact on cost effectiveness up to 6 months post initiation.
Time Frame
6 months
Title
Operation of the NMS
Description
The investigators will qualitatively describe the operation of the NMS, the complexity and nature of resulting consultations in terms of patient engagement, advice-giving and support. Additionally it will determine acceptability to stakeholders, reasons for success or lack of success, feasibility within the service delivery environment and generalisability and replicability across disease indications and community pharmacy settings
Time Frame
1 year from first recruited patient
Secondary Outcome Measure Information:
Title
Patients' understanding of their medicines
Description
The investigators will qualitatively evaluate patients' understanding of their medicines and the extent to which they are informed and supported in their medicines-related behaviour.
Time Frame
10 weeks
Title
Pharmacovigilance
Description
The investigators will qualitatively determine whether NMS encourages improved pharmacovigilance by community pharmacists and patients.
Time Frame
1 year from first recruited patient
Title
Stakeholder experience
Description
The investigators will qualitatively characterise patient (and/or carer) and professional experience.
Time Frame
1 year from first recruited patient
Title
Professional relationships
Description
The investigators will qualitatively explore inter-professional and patient-professional relationships.
Time Frame
1 year from first recruited patient

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Community dwelling patients eligible for NMS (aged from 14 years starting a new medicine for asthma/COPD, diabetes (Type 2), antiplatelet/anticoagulation or hypertension). Exclusion Criteria: Patients collecting a repeat prescription for a medicine (i.e. not new) for asthma/COPD, type 2 diabetes mellitus (T2DM), antiplatelets/anticoagulants or hypertension Patients collecting a medicine where the only change from the previous medicine involves a dosage or formulation change only Participants who are unable to understand patient/participant study documents Participants who are unable and unwilling to provide written consent / assent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthew J Boyd, PhD
Organizational Affiliation
University of Nottingham
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Rachel A Elliott, PhD
Organizational Affiliation
University of Nottingham
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Anthony J Avery, DM
Organizational Affiliation
University of Nottingham
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Nicholas Barber, PhD
Organizational Affiliation
University College, London
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rajnikant Mehta, MSc
Organizational Affiliation
University of Nottingham
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Justin Waring, PhD
Organizational Affiliation
University of Warwick
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Antony Chuter
Organizational Affiliation
Patient Involvement representative
Official's Role
Study Director
Facility Information:
Facility Name
Nottinghamshire County PCT/ County Health Partnerships
City
Nottingham
State/Province
Notts
Country
United Kingdom
Facility Name
Doncaster PCT
City
Doncaster
State/Province
South Yorkshire
Country
United Kingdom
Facility Name
Cambden, Barnet, Islington PCTs
City
London
Country
United Kingdom
Facility Name
Nottingham City PCT/Nottingham City Care
City
Nottingham
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
31732700
Citation
Elliott RA, Boyd MJ, Tanajewski L, Barber N, Gkountouras G, Avery AJ, Mehta R, Davies JE, Salema NE, Craig C, Latif A, Waring J, Chuter A. 'New Medicine Service': supporting adherence in people starting a new medication for a long-term condition: 26-week follow-up of a pragmatic randomised controlled trial. BMJ Qual Saf. 2020 Apr;29(4):286-295. doi: 10.1136/bmjqs-2018-009177. Epub 2019 Nov 15.
Results Reference
derived
PubMed Identifier
28776320
Citation
Elliott RA, Tanajewski L, Gkountouras G, Avery AJ, Barber N, Mehta R, Boyd MJ, Latif A, Chuter A, Waring J. Cost Effectiveness of Support for People Starting a New Medication for a Long-Term Condition Through Community Pharmacies: An Economic Evaluation of the New Medicine Service (NMS) Compared with Normal Practice. Pharmacoeconomics. 2017 Dec;35(12):1237-1255. doi: 10.1007/s40273-017-0554-9.
Results Reference
derived
PubMed Identifier
26647412
Citation
Elliott RA, Boyd MJ, Salema NE, Davies J, Barber N, Mehta RL, Tanajewski L, Waring J, Latif A, Gkountouras G, Avery AJ, Chuter A, Craig C. Supporting adherence for people starting a new medication for a long-term condition through community pharmacies: a pragmatic randomised controlled trial of the New Medicine Service. BMJ Qual Saf. 2016 Oct;25(10):747-58. doi: 10.1136/bmjqs-2015-004400. Epub 2015 Dec 8.
Results Reference
derived
PubMed Identifier
24289059
Citation
Boyd M, Waring J, Barber N, Mehta R, Chuter A, Avery AJ, Salema NE, Davies J, Latif A, Tanajewski L, Elliott RA. Protocol for the New Medicine Service Study: a randomized controlled trial and economic evaluation with qualitative appraisal comparing the effectiveness and cost effectiveness of the New Medicine Service in community pharmacies in England. Trials. 2013 Dec 1;14:411. doi: 10.1186/1745-6215-14-411.
Results Reference
derived
Links:
URL
http://www.NMSevaluation.org.uk
Description
NMS Study homepage

Learn more about this trial

Understanding and Appraising the New Medicine Service in England

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