RecruitingACTRN12620000430932

Integrating pharmacists in residential aged care facilities to improve quality use of medicine


Sponsor

University of Canberra

Enrollment

1,188 participants

Start Date

Jan 9, 2020

Study Type

Interventional

Conditions

Summary

This study will assess the efficacy, cost effectiveness and sustainability of having on-site pharmacist in residential aged care facilities (RACFs), as part of the care team, to improve the quality of use of medicine and reduce hospitalisations among RACF residents. Improved quality use of medication can reduce medication related adverse effects and hospitalisations. The study design is a cluster randomised controlled trial with RACFs in the ACT comparing RACFs with an on-site pharmacist for 2 or 2.5 day a week for 1 year, or usual care (no on-site pharmacist). Findings will inform practice and policy, leading to benefits for RACF residents care, safety and health care budgets.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

Residents in aged care facilities typically take many medications, which increases the risk of adverse drug reactions, harmful interactions, and unnecessary prescribing. Having a pharmacist embedded within the care team — rather than visiting occasionally — may allow medication-related problems to be identified and resolved much more quickly. This cluster randomised trial tests whether having an on-site pharmacist working 2–2.5 days per week in a residential aged care facility reduces hospitalisations and improves medication safety. Facilities in the ACT are randomly assigned to either have an on-site pharmacist or continue with usual care (no on-site pharmacist). Researchers track hospitalisation rates, medication-related incidents, and cost-effectiveness over one year. The findings will directly inform policy about pharmacist roles in aged care. You may be eligible as a resident if you are a permanent resident in a participating ACT aged care facility with more than 20 beds. Respite residents are not eligible for the study.

This is a simplified summary. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Integrating of on-site pharmacists in residential aged care facilities to improve the quality use of medicine and reduce hospitalisations of residential aged care residents. a) any physical/informati

Integrating of on-site pharmacists in residential aged care facilities to improve the quality use of medicine and reduce hospitalisations of residential aged care residents. a) any physical/informational materials used: Pharmacists will be given training in medications management in aged care and study outcomes. They will be provided with a pharmacist tool kit which provides information on study outcomes and relevant guidelines. b) the procedures, activities, and/or processes used: RACFs in the intervention arm will have a pharmacist integrated into the health care team for 2 or 2.5 days a week (depending on RACF size) for the duration of 12 months. The pharmacist will improve the quality use of medicines through pharmacist activities that are within their current scope of practice as an Australian health professional registered with Australian Health Professional Registered Agency (AHPRA). Pharmacist activities include: • Medication Reviews • Identifying residents at high risk of hospitalisation and prioritising interventions • Vaccination of resident and staff against influenza • Medication reconciliation/review at transition of care • Reviewing and optimising medication rounds • Updating and verifying resident’s clinical information • Answering medication related queries from resident, families and staff • Improving resident’s clinical documentation • Conducting regular clinical audits • Contributing to policies and procedures and education staff about medication management c) what the study involves for participants: RACF residents in the intervention arm will have medication reviews conducted by the pharmacist at transitions of care. This may result in pharmacists discussing medications with residents, and recommendations sent to GPs and other health professionals such as Nurse Practitioners, specialist palliative care, dietitians, and Occupational Therapists. d) the mode of delivery: Face to face. e) the number of times the intervention will be delivered and over what period of time: RACFs in the intervention arm will have a pharmacist integrated into the health care team for 2 or 2.5 days a week (depending on RACF size) for the duration of 12 months f) any strategies used to assess or monitor adherence or fidelity to the intervention (if applicable): The research team will monitor intervention sites for fidelity to the intervention, using two methods informed by Hasson’s Conceptual Framework (2012), that assesses adherence against content, coverage, frequency and duration domains. First, 100% of pharmacist diaries in each intervention RACF will be assessed and cumulative number/proportion of activities will be calculated. Second, a random sample of 10% of intervention RACF medications reviews [of those received a review] will be checked against resident charts by an experienced pharmacist/PI/research team to determine the appropriateness of medications review. Third, interviews with RACF managers/staff and pharmacists will be assessed regarding site buy-in to the model of care, for example, engagement in conducting trial activities. Sites will be given a fidelity rating of high/medium/low based on the assessment.


Locations(1)

ACT, Australia

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ACTRN12620000430932


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