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Senior Center Medication Safety and Empowerment Curriculum

Team Alice Senior Center Medication Safety and Empowerment Curriculum

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07799610
Enrollment
125
Registered
2026-09-02
Start date
2026-02-01
Completion date
2027-03-31
Last updated
2026-09-02

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

Conditions

Caregiver Awareness, Empowerment, Patient, Health Literacy, Knowledge, Medication and Supplement Use, Older Adults

Keywords

older adult, patient education, caregiver education, medication safety, patient knowledge, patient empowerment

Brief summary

Team Alice's Medication Safety and Empowerment Curriculum (MedSEC) helps older adults and caregivers learn how to safely manage medications. Many seniors take multiple medications, which can lead to harmful side effects or unnecessary treatments. This program, developed at the University at Buffalo, will be offered at senior centers in Western New York. It includes two interactive sessions that teach participants how to recognize medication risks and talk with their doctors about safer options. The curriculum uses videos, group discussions, and hands-on tools to build confidence and knowledge. It follows the "4Ms" of Age-Friendly Health Systems: What Matters, Medication, Mentation, and Mobility. A "Train-the-Trainer" model will help senior center staff continue the program long-term. The goal is to reduce medication harm, improve communication with healthcare providers, and support healthy aging in the community.

Interventions

OTHERTeam Alice Medication Safety and Empowerment Curriculum (MedSEC)

A two-part interactive curriculum that will improve medication safety awareness and empower participants to engage in conversations with healthcare providers. The focus of this study will be to evaluate the impact of the MedSEC on patient/care-partner knowledge and medication management patient activation levels. A pre/post study that surveys older adults/caregivers pre-curriculum intervention and post-curriculum intervention, in addition to 6 months after program completion.

Sponsors

State University of New York at Buffalo
Lead SponsorOTHER
Health Foundation for Western and Central New York
CollaboratorUNKNOWN

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* 55 years of age and above * taking prescription medications Carepartner Inclusion Criteria: * currently an informal or formal care partner for an eligible patient (regardless of whether they live with or near the patient) * aged 18 years of age and above

Exclusion criteria

* Patients with cognitive impairment that prevents their self-management of medications.

Design outcomes

Primary

MeasureTime frameDescription
Evaluate the impact of the MedSEC on patient/care-partner knowledge and activation levels in managing medications through the Patient Activation Measure (PAM)Change from baseline (Day 1), post-program assessment (immediately after educational session 2, Day 7), and 6 months after program completion.Study seeks to enhance patient and care-partner activation, reduce polypharmacy and the use of potentially inappropriate medications (PIMs), and improve shared decision-making through the Patient Activation Measure (PAM).
Evaluate the impact of the MedSEC on patient/care-partner knowledge and activation levels in managing medications through the Revised Patient Attitudes Towards Deprescribing (rPATD) questionnaires.Change from baseline (Day 1), post-program assessment (immediately after educational session 2, Day 7), and 6 months after program completion.Study seeks to enhance patient and care-partner activation, reduce polypharmacy and the use of potentially inappropriate medications (PIMs), and improve shared decision-making through the Revised Patient Attitudes Towards Deprescirbing (rPATD) questionnaires.

Secondary

MeasureTime frameDescription
Change from Baseline in participant understanding of medication safety risks at 6 Months.Change from baseline (Day 1), post-program assessment (immediately after educational session 2, Day 7), and 6 months after program completion.85% of participants will demonstrate an understanding of medication safety risks through pre- and post-program patient/caregiver questionnaires, including the Patient Activation Measure (PAM) and Revised Patient Attitudes to Deprescribing (rPATD). Additional questions pertaining to knowledge retention and actionability will be asked at 6 months.
Participants will demonstrate knowledge of the 4Ms (Age-Friendly Health System) framework through pre/post/6 month follow up questionnaires.Change from baseline, post-program assessment (immediately after program completion), and 6 months after program completion.By the end of the program, 80% of participants will demonstate knowledge of the 4Ms framework, measured by four questions related to the 4Ms and the Age-Friendly Health System taken prior to the program, immediately post-program, and 6 months after program completion.
Change in patient engagement as measured by the Patient Activation Measure (PAM) from baseline to 6 months post program.Change from baseline (Day 1), post-program assessment (immediately after educational session 2, Day 7), and 6 months after program completion.6 months post-program, 65% of participants will show improved patient engagement, as measured by the Patient Activation Measure (PAM) questionnaire.
Change from baseline in the mean of medications after 6 months follow-upChange from baseline and 6 months after program completion.Within 6 months of completing program, 50% of participants with polypharmacy will have reduced medication usage by 10%. (mean # of medications.)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 3, 2026