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临床试验/NCT04023734
NCT04023734已完成不适用

A Targeted and Tailored Pharmacist Intervention to Improve Adherence to Antihypertensive Drugs Among Patients With Diabetes in Indonesia: a Cluster Randomized Controlled Trial

University of Groningen1 个研究点 分布在 1 个国家目标入组 113 人开始时间: 2019年8月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
113
试验地点
1
主要终点
Medication adherence

研究概览

简要总结

The primary objective of this study is to assess the effect of a targeted and tailored pharmacist intervention on medication adherence among diabetes patients non-adherent to antihypertensive drugs. The secondary objectives are to assess the effect of the intervention on blood pressure level and medication beliefs, and to evaluate the implementation and adoption of the intervention for pharmacists and patients.

详细描述

Adherence to chronic medication is often suboptimal. However, existing interventions to improve adherence are either too complex or expensive for implementation and scale-up in low-middle income countries and/or not particularly effective.

A cluster randomized controlled trial with 3-months follow-up will be conducted in 10 Community Health Centers (CHCs) in Indonesia. Patients aged ≥18 years, diagnosed with type 2 diabetes and reported non-adherence to antihypertensive drugs according to the Medication Adherence Report Scale (MARS) are eligible to participate. Patients in the five CHCs randomized to the intervention group will receive a targeted and tailored pharmacist intervention at baseline (first session) and at 1-month follow-up (second session). The intervention will be low-cost, align with the current CHC workflow and will not require a substantial change to the current system. Before dispensing antihypertensive drugs during the first session, the pharmacist will discuss patient-specific barrier(s) for medication adherence based on their responses on MARS and three additional questions, which are derived from the Brief Medication Questionnaires. The intervention strategies will then be tailored to their identified adherence problems. Based on current literature, the investigators defined four non-adherence problems that can be addressed by the community pharmacist, i.e. (1) forgetfulness, (2) lack of knowledge, (3) lack of motivation or (4) other drug-related problems. Of note, patients might need a combined intervention strategy to address all experienced problems. The four non-adherence problems and recommended intervention strategies are specified below:

  1. Strategies to cope with forgetfulness include reminders, habit-based strategies and/or involvement of family members.
  2. The content of the counselling to cope with lack of knowledge will focus on educating patients about about the purpose of the medication, when and how to take the medication, the need for long-term use, the importance of medication adherence, and how to deal with possible side effects. To explore which education is needed, the patient will be asked whether they know why and how to take their medication. The teach-back method will be used, where the patient is asked to explain the pharmacist what he/she has understood after receiving the education.
  3. The content of the counselling to cope with lack of motivation will focus on exploring and discussing the patients' concerns and necessity beliefs (motivational interviewing).
  4. The content of the counselling to address other drug related problems will focus on exploring other problems underlying the non-adherence, for example experiencing side effects, costs, polypharmacy, difficulty to refill antihypertensive drugs in time, or medication intake problems, and offering solutions/alternatives when possible.

The follow-up session will be conducted in one month after the baseline session, when patients refill their medication at the next regular outpatient visit. The purpose of the follow-up session is (1) to evaluate the short-term effect of the intervention and discuss the patients' implementation of and experiences with the offered information and recommendations, and (2) to address non-adherence problems that were not yet addressed during the first session. Where needed, the pharmacist, together with patient, can make changes to the coping plan and discuss additional interventions. As the quality of the intervention will depend on the competences and skills of the pharmacist, treatment integrity will be enhanced by an obligatory communication training focusing on motivational interviewing and the teach-back method, and by providing supportive material as part of the intervention.

Patients in five CHCs randomized to the control group will receive pharmacist counselling based on the Indonesian guideline of pharmacy practice. At each visit, they can receive information about the quantity and dose of the dispensed drugs, when and how to use and store the drugs, side effects and how to deal with them, the importance of medication adherence, and confirming if the patient understands how to take medications correctly. Patients in the control group will complete all assessments at the same time points as those in the intervention group

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • At least 18 years old.
  • Diagnosed with type 2 diabetes for at least one year based on patient's medical record.
  • Using at least one antihypertensive drug in the last three months.
  • Provision of signed informed consent.
  • Have sub-optimal medication adherence to antihypertensive drugs according to the MARS (<20).

排除标准

  • Patients with severe mental or physical constraints.
  • Pregnancy or in the lactation period.
  • Illiterate in Indonesian language.
  • Enrollment in another intervention study.
  • Those not responsible for taking their own medication

结局指标

主要结局

Medication adherence

时间窗: Baseline, 1-month, and 3-month follow-up

The differences in change in total score of medication adherence using Medication Adherence Report Scale (MARS). The Indonesian version of the MARS showed to be valid (correlation value of each question to the total score \> 0.396) and reliable (Cronbach α coefficient of 0.803). Patients will indicate how often each statement applied to them on a 5-point Likert scale ranging from always (score 1) to never (score 5). Items are summed to obtain a total score ranging from 5 to 25.

次要结局

  • Reach(On completion of the final assessments at 3-month follow-up.)
  • Pharmacists' adoption of the intervention(On completion of the final assessments at 1-month follow-up.)
  • Patients' adoption of the intervention(On completion of the final assessments at 3-month follow-up.)
  • Blood pressure level(Baseline, 1-month, and 3-month follow-up)
  • Medication beliefs(Baseline and 3-month follow-up)
  • Pharmacists' suggestions for future implementation(On completion of the final assessments at 1-month follow-up.)
  • Patients' suggestions for future implementation(On completion of the final assessments at 3-month follow-up.)
  • Pharmacists' willingness to maintain the intervention(On completion of the final assessments at 1-month follow-up.)
  • Patients' willingness to maintain the intervention(On completion of the final assessments at 3-month follow-up.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sofa Dewi Alfian

Registered pharmacist

University of Groningen

研究点 (1)

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