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Pharmacist involvement in helping patients at discharge from hospital and the effect on their wellbeing and readmission to hospital

Pharmacist involvement to enhance identification and management of patients at discharge from hospital with increased risk of medication related problems and effect on quality of life and readmission to hospital: a double arm, randomised clinical trial.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616001474448
Enrollment
700
Registered
2016-10-24
Start date
2016-11-14
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

During your hospital stay your medicines may change. The aim of this project is to find out if patients who get extra education from a pharmacist when being discharged mean they can manage any changes better. We also want to find out if the pharmacist work has an impact on readmission to hospital and quality of life. This project needs two groups of patients. One will receive the usual standard of quality care and will complete a brief questionnaire to measure your ‘quality of life’. The second group will complete the same questionnaire and have some additional time with a specialised pharmacist. By doing this we can see if there is any difference between the 2 groups and work out if the extra pharmacist time reduces readmission to hospital and improves patients’ quality of life.

Interventions

For patients enrolled to the intervention arm, they will be provided with the current standard of care (which involves a clinical review of medications, some may have a medicines reconciliation on admission (they qualify for this based on the local criteria for this), counselling on only specific medications such as warfarin or home intravenous antibiotics) by the ward pharmacist AND a more comprehensive, individualised discharge service by the study pharmacist. This will occur only on discharge

For patients enrolled to the intervention arm, they will be provided with the current standard of care (which involves a clinical review of medications, some may have a medicines reconciliation on admission (they qualify for this based on the local criteria for this), counselling on only specific medications such as warfarin or home intravenous antibiotics) by the ward pharmacist AND a more comprehensive, individualised discharge service by the study pharmacist. This will occur only on discharge from hospital as a single event (if the patient is to go home outside of pharmacy hours, the discharge service will occur the next working day and education will occur via telephone) The discharge service is expected to take up to an hour (however this will vary patient to patient). It will include: Patient counselling of medicines Discharge medication reconciliation Organise a compliance aid if necessary Returning patient’s own medicines Medication card and medicine information leaflets Assist with access to medication Review of the medication related information on the discharge summary Comprehensive General Physician and community pharmacist handover (including medication changes, discharge medication list, ongoing monitoring, any drug interactions) If deemed necessary, a referral to a Clinical Pharmacist working in the PHO The participants will also be asked to complete a single question health literacy test and a quality of life survey. Every intervention provided to each participant will be documented on an 'intervention' form for analysis at the end of the trial.

Sponsors

Health Research South
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Eligible participants are adult (over 18 years) patients being treated on the Internal Medicine ward at Dunedin Hospital who are identified as being high risk for readmission by an electronic prioritisation tool. Patients meet inclusion criteria if they are allocated a certain score using a prioritisation tool on admission. The cut off score for inclusion is still to be decided (the electronic tool validation is underway currently).

Exclusion criteria

Patients who don't meet a certain score by the electronic prioritization tool (that identifies those at high risk for readmission) will be excluded from the study. Those who are unable to provide informed consent will be excluded from the study.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026