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临床试验/ISRCTN15089342
ISRCTN15089342进行中(未招募)Unknown

Medication brand changes in hormone therapy for breast cancer. A community pharmacy intervention development to improve patients’ adherence and quality of life

ondon Metropolitan University0 个研究点目标入组 45 人开始时间: 2024年6月25日最近更新:
适应症

试验速览

阶段
Unknown
状态
进行中(未招募)
发起方
入组人数
45

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • WP1 - 1.c Qualitative interviews with pharmacists:
  • 1.Pharmacists who are owner or manager of a community pharmacy, chain and independent;
  • 2.pharmacists with a representative role in professional pharmaceutical bodies, e.g. Local Pharmaceutical Committee, Community Pharmacy England, Royal Pharmaceutical Society.
  • WP2 - 2b. Qualitative interviews with pharmacists:
  • 1.A pharmacist or pharmacist technician, permanent or locum (and)
  • 2.Working in community pharmacies located in London (and)
  • 3.Providing hormone therapy medication to clients
  • WP3 – Testing and optimisation studies
  • Pharmacists:
  • 1.Pharmacists and pharmacy technicians; from the London boroughs of Barnet, Camden, Enfield, Haringey, or Islington
  • 2.Providing Hormone Therapy medication to clients
  • 3.Agree to participate in online training
  • 4.Agree to recruit 4 patients from their pharmacy
  • 5.Agree to deliver a medication consultation with recruited participants and audio record 1 consultation (with patient consent), and provide feedback notes of the consultation.
  • 6.Agree to provide feedback in a study follow-up interview.
  • 7.Is willing to provide written (signed and dated) informed consent.
  • 1.Women 18+ with early BC (stage 1-3);
  • 2.Talking oral HT medication (tamoxifen, anastrozole, or letrozole) and had/have concerns about changing HT brands;
  • 3.Not taking HT medication as neo-adjuvant or secondary metastatic BC;
  • 4.Is willing and able to record notes on side effects and medication taken (diary) and attend a medication consultation with the CP;
  • 5.Is willing and able to participate in a study follow-up interview (phone or video conference);
  • 6.Is willing to provide a copy of the diary;
  • 7.Is willing to be audio recorded during the pharmacy consultation;
  • 8.Is willing to provide written (signed and dated) informed consent.

排除标准

  • WP1 - 1.c Qualitative interviews with pharmacists:
  • 1.locum, technician, assistants, pharmacist not owner or manager
  • 2.Pharmacists without a representative role in professional pharmaceutical bodies
  • WP2 - 2b. Qualitative interviews with pharmacists:
  • 1.Accredited Checking Technician, assistants
  • WP3 – Testing and optimisation studies
  • Pharmacists:
  • 1.Locum, Accredited Checking Technician, pharmacy assistants.
  • 2.Currently or recently (last 6 months) involved in another research study where medication adherence is a primary outcome;
  • 3.Have had in the last 6 months a medication review about changing brands of HT drugs.

研究者

发起方
ondon Metropolitan University

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