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

27. mai 2015 oppdatert 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

Studieoversikt

Studietype

Intervensjonell

Registrering (Faktiske)

504

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

14 år og eldre (Barn, Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Støttende omsorg
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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
Ingen inngripen: Current Practice
Patients in this arm will receive the normal advice with their new medicine as dictated by current professional practice

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Medicines adherence
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Patients' understanding of their medicines
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 1 year from first recruited patient
The investigators will qualitatively explore inter-professional and patient-professional relationships.
1 year from first recruited patient

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

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

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. august 2012

Primær fullføring (Faktiske)

1. april 2014

Studiet fullført (Faktiske)

1. april 2014

Datoer for studieregistrering

Først innsendt

19. juni 2012

Først innsendt som oppfylte QC-kriteriene

3. juli 2012

Først lagt ut (Anslag)

9. juli 2012

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

28. mai 2015

Siste oppdatering sendt inn som oppfylte QC-kriteriene

27. mai 2015

Sist bekreftet

1. mai 2015

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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