Can a pharmacist check-in boost medication adherence in diabetes and kidney disease?
NCT ID NCT04190251
First seen Jul 17, 2026 · Last updated Jul 17, 2026
Summary
This study tests a support program for people with type 2 diabetes and chronic kidney failure who struggle to take their medications regularly. Participants receive an electronic pill bottle that tracks when they open it, plus short motivational interviews with a pharmacist. The goal is to see if this combination helps them stick to their medication routine over 6 to 12 months, compared to usual care alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Interprofessional medication adherence support program (IMAP) combining electronic monitoring and motivational interviews
- What this could lead to
- If successful, this program could offer a practical way to help patients with diabetes and kidney disease stick to their medications, potentially improving health outcomes.
- What could go wrong
- This is a small, single-center study with 73 participants, so results may not apply broadly. The program requires extra pharmacy visits, which may not suit everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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73 people
The number who actually took part.
- Started
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Apr 2016
- Finished
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Dec 2022
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * MDRD or CKD-EPI eGFR ≤60 ml/min/1.73m2 or albumin/creatinin \>30mg/mmol * Type 2 diabetes * At least one medication in the following list : oral antidiabetics and/or statins and/or antihypertensive drugs and/or aspirin * Patients speaking french, english or italian or interpreter present at each pharmacy visit * Patients have to sign the written consent form * Patients have to agree to use the Electronic Monitoring system (EM, named MEMS®; Aardex Ltd) * Complete laboratory exams in the last 6 months: eGFR and HbA1c and (albumin/creatinin ratio or total cholesterol + LDL + HDL) Exclusion Criteria: * Not being able to understand or sign the consent form * Pregnancy * Recent cancer diagnosis * Cognitive disorder * The subject does not manage the treatment alone
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Centre Hospitalier Universitaire Vaudois
Lausanne, Canton of Vaud, 1011, Switzerland
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Unisante
Lausanne, Canton of Vaud, 1011, Switzerland
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