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Blister Packaging Medication to Increase Treatment Adherence and Clinical Response

Blister Packaging Medication to Increase Treatment Adherence and Clinical Response: Impact on Suicide-Related Morbidity and Mortality

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01118208
Acronym
BP
Enrollment
303
Registered
2010-05-06
Start date
2009-09-30
Completion date
2014-09-30
Last updated
2017-10-20

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

Conditions

Accidental Overdose, Deliberate Overdose, Medication Adherence, Suicide, Attempted

Keywords

Medication adherence, Accidental overdose, Deliberate overdose, Suicide, attempted

Brief summary

This quantitative, interview-based study will determine if increased prescription medication adherence via blister pack administration will reduce suicide related behavior among the high risk population of patients discharged from a psychiatric inpatient unit. The aims of the project are to determine whether blister packaging medication significantly increases treatment adherence and if blister packaging significantly decreases intentional self-poisoning behavior (i.e., suicide attempts and completions). By tracking former psychiatric inpatients for 12 months post-discharge and obtaining monthly medication adherence ratings, we will determine if blister packaging (BP) medications leads to better adherence than dispensing as usual (DUA). The psychiatric patients we will be recruiting have been diagnosed with, major affective disorder, bipolar affective disorder, post-traumatic stress disorder, or schizophrenia (or any combination of these diagnoses). By tracking former psychiatric patients for 12 months post-discharge and obtaining monthly reports (self-report and medical record review) of suicide-related behaviors, we will determine if patients in the BP condition have less intentional self-poisoning behavior than those in the DAU condition.

Interventions

OTHERBlister packaging medications

Dispensing prescription medications on pre-filled blister package cards.

OTHERDispense as usual

Dispensing prescription medications in standard pill bottles.

Sponsors

United States Department of Defense
CollaboratorFED
VA Eastern Colorado Health Care System
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* age 18 or older * diagnosed with major affective disorder, * bipolar affective disorder, * post-traumatic stress disorder, or * schizophrenia (or any combination of these diagnoses) * under voluntary status at some point during admission * currently prescribed medications * deemed capable of managing their own medications after discharge * not currently active duty in any branch of the military * able to correctly answer questions verifying they understand the consent form * English-Speaking

Exclusion criteria

* Under the age of 18 * Not under voluntary status at some point during admission * Not currently prescribed medications * Not able to manage their own medications after discharge * Non-English-speaking * Currently active duty in any branch of the military * Inability to correctly answer questions indicating comprehension of information on the consent form

Design outcomes

Primary

MeasureTime frame
Medication Adherence as assessed with the Brief Adherence Rating Scale (BARS)monthly for 12 months

Secondary

MeasureTime frameDescription
Medication overdoses as measured by the Self-Harm Behavior Questionnaire (SHBQ)monthly for 12 monthsBoth accidental and intentional overdoses will be assessed.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026