A Targeted and Tailored Pharmacist Intervention to Improve Adherence to Antihypertensive Drugs Among Diabetes Patients

Not Applicable

Completed

• Conditions: Diabetes Mellitus, Type 2; Hypertension; Medication Nonadherence
• Interventions: Behavioral: Usual care based on the Indonesian guideline; Behavioral: Reminders, habit-based strategies and/or involvement of family member; Behavioral: Counselling to increase knowledge; Behavioral: Counselling to increase motivation; Behavioral: Explore/address other drug related problems

• Registration Number: NCT04023734
• Lead Sponsor: University of Groningen

Brief Summary

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.

Detailed Description

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

The primary study outcome is the difference between intervention and control group in change in total adherence scores using the MARS between baseline and 3 months follow-up. Secondary outcomes are blood pressure (BP), medication beliefs using the Beliefs about Medicines Questionnaire (BMQ)-specific, and evaluate the intervention using the RE-AIM framework (Reach, Effectiveness, Adoption, Implementation, and Maintenance).

Study Timeline

• Study First Submitted: 2019-06-26
• Study First Submitted QC: 2019-07-16
• Study First Posted: 2019-07-17
• Study Start: 2019-08-16
• Primary Completion: 2019-12-30
• Study Completion: 2020-01-30
• Status Verified: 2020-03
• Last Update Submitted: 2020-03-23
• Last Update Posted: 2020-03-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 113

Inclusion Criteria

• 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).

Exclusion Criteria

• 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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Control group	Usual care based on the Indonesian guideline	Usual care based on the Indonesian guideline at baseline and 1-month follow-up.
Intervention	Counselling to increase knowledge	A targeted and tailored pharmacist intervention at baseline and at 1-month follow-up.
Intervention	Reminders, habit-based strategies and/or involvement of family member	A targeted and tailored pharmacist intervention at baseline and at 1-month follow-up.
Intervention	Counselling to increase motivation	A targeted and tailored pharmacist intervention at baseline and at 1-month follow-up.
Intervention	Explore/address other drug related problems	A targeted and tailored pharmacist intervention at baseline and at 1-month follow-up.

Primary Outcome Measures

Name	Time	Method
Medication adherence	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.

Secondary Outcome Measures

Name	Time	Method
Reach	On completion of the final assessments at 3-month follow-up.	Reach will be assessed by measuring the participation rates and representativeness of patients who participate in this study. In case a patient refuses or discontinues to participate in this study, patient's age, gender, and BP lowering drugs the patient uses will be recorded by research assistants. This information is used to calculate the participation rate and assess differences between responders and non-responders. To determine representativeness, patient's demographics will be compared to census demographics in Bandung City, Indonesia.
Pharmacists' adoption of the intervention	On completion of the final assessments at 1-month follow-up.	Pharmacists' adoption with various parts of the intervention will be assessed by focus group discussion (FGD). Example of questions: * What do you think of the program in general?(Regarding number of sessions, time between sessions, duration of sessions); * Tell me about positive experiences you have had with the program. Do others agree? Do others have different experiences?; * Tell me about negative experiences you have had with the program. Do others agree? Do others have different experiences?
Patients' adoption of the intervention	On completion of the final assessments at 3-month follow-up.	Patients' adoption with various parts of the intervention will be assessed by a questionnaire (e.g How satisfied are you with the information provided by the pharmacist regarding your antihypertensive drugs during the past three months?)
Blood pressure level	Baseline, 1-month, and 3-month follow-up	Within and between patient changes in blood pressure (BP) level (systolic blood pressure \[SBP\] and diastolic blood pressure \[DBP\]) at baseline, 1-month, and 3-month follow-up. BP measurements will be performed by a nurse who is blinded to the group assignment.
Medication beliefs	Baseline and 3-month follow-up	Within patient changes on beliefs about medication will be assessed using the BMQ-specific at baseline and 3-month follow-up. The BMQ-specific contains 5 items about necessity beliefs (e.g. "My health at present depends on my blood pressure-lowering medicines"), and 5 items about concern beliefs (e.g. "I sometimes worry about becoming too dependent on my blood pressure-lowering medicines"). All items have a 5-point Likert scale ranging from strongly disagree to strongly agree with an overall range from 5 (low necessity, low concern) to 25 (high necessity, high concern). A necessity-concern differential score will be calculated by subtracting the scores of the concerns scale from the necessity scale (range -20 to 20). A positive differential score indicates stronger beliefs in the necessity, while a negative score indicates stronger concerns.
Pharmacists' suggestions for future implementation	On completion of the final assessments at 1-month follow-up.	Pharmacists' suggestions for future implementation of the intervention will be assessed by FGD with following questions: * Suppose that you were in charge, do you think this program could be implemented in your CHC?; * Please explain why or why not.; * What do others think?; * What do you see as barriers?; * What would help to support the implementation?
Patients' suggestions for future implementation	On completion of the final assessments at 3-month follow-up.	Patients' suggestions for future implementation of the intervention will be assessed by a questionnaire (e.g How could we improve the program?)
Pharmacists' willingness to maintain the intervention	On completion of the final assessments at 1-month follow-up.	Pharmacists' willingness to continue the intervention as part of routine clinical practice over the long term will be assessed by FGD with the following questions: * Suppose that this program is implemented, do you think this program will sustain in your CHC? - Please explain why or why not.; * What do others think?; * What do you see as barriers?; * What would help to sustain this program?
Patients' willingness to maintain the intervention	On completion of the final assessments at 3-month follow-up.	Patients' willingness to continue the intervention as part of routine clinical practice over the long term will be assessed by a questionnaire (e.g Suppose that this program will be implemented in the future, how often would you like to receive it?)

Trial Locations

Locations (1)

Community Health Centers; 🇮🇩 Bandung, West Java, Indonesia