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

27 maj 2015 uppdaterad av: University of Nottingham

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

Studieöversikt

Studietyp

Interventionell

Inskrivning (Faktisk)

504

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • London, Storbritannien
        • Cambden, Barnet, Islington PCTs
      • Nottingham, Storbritannien
        • Nottingham City PCT/Nottingham City Care
    • Notts
      • Nottingham, Notts, Storbritannien
        • Nottinghamshire County PCT/ County Health Partnerships
    • South Yorkshire
      • Doncaster, South Yorkshire, Storbritannien
        • Doncaster PCT

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

14 år och äldre (Barn, Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Stödjande vård
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: NMS
Patients in this arm will receive the full NMS service
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
Inget ingripande: Current Practice
Patients in this arm will receive the normal advice with their new medicine as dictated by current professional practice

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Medicines adherence
Tidsram: Change in adherence from 6 weeks to 10 weeks and 26 weeks
Patients will report medicines adherence using the service specified adherence question and against standard adherence scales
Change in adherence from 6 weeks to 10 weeks and 26 weeks
Cost effectiveness
Tidsram: 6 months
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.
6 months
Operation of the NMS
Tidsram: 1 year from first recruited patient
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
1 year from first recruited patient

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Patients' understanding of their medicines
Tidsram: 10 weeks
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.
10 weeks
Pharmacovigilance
Tidsram: 1 year from first recruited patient
The investigators will qualitatively determine whether NMS encourages improved pharmacovigilance by community pharmacists and patients.
1 year from first recruited patient
Stakeholder experience
Tidsram: 1 year from first recruited patient
The investigators will qualitatively characterise patient (and/or carer) and professional experience.
1 year from first recruited patient
Professional relationships
Tidsram: 1 year from first recruited patient
The investigators will qualitatively explore inter-professional and patient-professional relationships.
1 year from first recruited patient

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Studierektor: Anthony J Avery, DM, University of Nottingham
  • Studiestol: Matthew J Boyd, PhD, University of Nottingham
  • Studiestol: Rachel A Elliott, PhD, University of Nottingham
  • Huvudutredare: Nicholas Barber, PhD, University College, London
  • Studierektor: Rajnikant Mehta, MSc, University of Nottingham
  • Studierektor: Justin Waring, PhD, University of Warwick
  • Studierektor: Antony Chuter, Patient Involvement representative

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Allmänna publikationer

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 augusti 2012

Primärt slutförande (Faktisk)

1 april 2014

Avslutad studie (Faktisk)

1 april 2014

Studieregistreringsdatum

Först inskickad

19 juni 2012

Först inskickad som uppfyllde QC-kriterierna

3 juli 2012

Första postat (Uppskatta)

9 juli 2012

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

28 maj 2015

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

27 maj 2015

Senast verifierad

1 maj 2015

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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