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Partnership in Medication Management (PIMM) in Patients With Mood Disorders

Partnership in Medication Management (PIMM): The Effects of One-on-one Medication Training on Medication Adherence in Patients With Mood Disorders

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02285608
Acronym
PIMM
Enrollment
166
Registered
2014-11-07
Start date
2015-01-31
Completion date
2017-05-31
Last updated
2015-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bipolar Disorder, Major Depressive Disorder

Keywords

Medication adherence, Patient education, Mood disorders, Economic assessment, Mixed methods

Brief summary

Investigators are doing this study to examine if a new personalized education program for patients with mood disorders (depression and bipolar disorders) will help them take their medications as prescribed by doctors. Investigators will teach patients about how, when and why it is important for them to take their medications as prescribed. Also, investigators will ask patients why they do not take medications as prescribed. Furthermore, investigators will examine whether our education program might save money if it prevents problems related to not taking medication.

Detailed description

The efficacy of anti-depressants or lithium reported in clinical trials differs from clinical experience. Various factors such as non-adherence to treatment and poor tolerability to medications have been related to treatment non-response or treatment failure in mood disorders (major depressive disorder and bipolar disorder). Premature discontinuation of treatment for mood disorders is common. The long treatments, the patients' beliefs about medications, the lack of knowledge about the medication/treatment purpose, benefits, dosage, and side effects and the relationship between patient and healthcare providers affect treatment continuation. Investigators are proposing a sequential explanatory mixed methods study to investigate a novel program for medication training in persons with mood disorders. The ultimate purpose of the program is to improve medication adherence in these persons. The primary component of the present study will be quantitative, i.e., a randomized controlled trial with 12 months of follow-up to examine the effect of one-on-one medication training, including the use of a checklist system, on medication adherence in patients with mood disorders. The training program will include education to improve patients' knowledge regarding their medication's purpose, dosage, benefits, and side effects. The program will also include tools like a checklist or alarm clock to remind patients of when and how to take their medication. Furthermore, the program will contain an interactive listening period where healthcare professionals involved in medication dispensing will listen to patients' concerns, questions and thoughts regarding their medications. To the best of the investigators' knowledge, no research has comprehensively examined whether one-on-one medication training, as described above, may improve medication adherence in patients with mood disorders.

Interventions

OTHERPIMM/SAM

The PIMM program will include education to improve patients' knowledge regarding their medication's purpose, dosage, benefits, and side effects. The program will also include tools like a checklist or alarm clock to remind patients of when and how to take their medication. Furthermore, the program will contain an interactive listening period where healthcare professionals involved in medication dispensing will listen to patients' concerns, questions and thoughts regarding their medications.

Sponsors

St. Joseph's Healthcare Hamilton
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* admitted to the inpatient clinic of the Mood Disorders Program, St. Joseph's Healthcare Hamilton * with a primary diagnosis of bipolar disorder I or II, or major depressive disorder * able to speak, read, and understand English.

Exclusion criteria

* cut off score on Montreal Cognitive Assessment (MOCA; clinical judgement) * significant suicidal or homicidal risk * a medical condition/treatment known to affect the brain * acquired brain injury.

Design outcomes

Primary

MeasureTime frameDescription
Medication adherence measured by the Medication Adherence Rating Scale (MARS).Change from baseline in the Medication Adherence Rating Scale at 2 days before discharge and 1 week, 1 month, 3 months, 6 months and 12 months post-dischargeMedication adherence measured by the Medication Adherence Rating Scale (MARS). We will measure medication adherence at baseline and each follow up

Secondary

MeasureTime frameDescription
Time to re-hospitalizationFirst time re-hospitalization any point during the 12-month follow-up periodInvestigators will compare the time to re-hospitalization between each study group.
Costs of re-hospitalizationFirst time re-hospitalization any point during the 12-month follow-up periodInvestigators will adopt a healthcare system perspective and compare the costs of first re-hospitalization between each study group. When a participant is re-hospitalized for the first time at any point during the 12-month follow-up period, investigators will conduct a chart review of the entire re-hospitalization to identify all of the direct and indirect medical resources consumed during this re-hospitalization. The chart review will cover the entire length of the re-hospitalization, even if this length exceeds the 12-month follow-up period for the participant in question.

Countries

Canada

Contacts

Primary ContactCarolina Oremus, MD, PhD(c)
coremus@stjoes.ca+1(905) 522-1155
Backup ContactMargaret C McKinnon, PhD,C.Psych.
mmckinno@stjoes.ca+1(905) 522-1155

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026