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Testing of a new community pharmacy service to help older patients who live in their own homes and who are prescribed several medicines

Feasibility testing of the ID-MAP (IDentification of Medication Adherence Problems) intervention in older adults prescribed polypharmacy in primary care

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17966504
Enrollment
14
Registered
2016-12-01
Start date
2016-03-18
Completion date
Unknown
Last updated
2018-08-27

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

Conditions

Non-adherence to polypharmacy in older adults Not Applicable

Interventions

The intervention will be delivered to non-adherent older adults by a trained community pharmacist over three (30-40 minute) appointments held within the community pharmacy. At Appointment 1, the pharm

Sponsors

Queen's University Belfast
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Community pharmacist participants: 1. Located in Northern Ireland 2. At least one pharmacist (maximum 2) willing to take part in the study and provide written informed consent 3. Access to a private consultation room/area 4. Access to printing facilities Patient participants: 1. Aged 65 years or older 2. Prescribed four or more regular medications (excluding medications prescribed to be taken only when required or medicines purchased over-the-counter) 3. Living in their own home 4. Have at least six months of dispensing data available from the time of screening (on the pharmacy-held Patient Medication Record) 5. Only attend the study site pharmacy for regular medications 6. Have an identified adherence problem (detected using self-report adherence questionnaire)

Exclusion criteria

Exclusion criteria: Community pharmacist participants: 1. Not meeting the inclusion criteria 2. Not proving written informed consent Patient participants: 1. Not meeting the inclusion criteria 2. Not providing written informed consent 3. Prescribed medications for the treatment or management of dementia (e.g. donepezil, galantamine, rivastigmine or memantine) 4. Unable to complete the Eligibility Screening Questionnaire 5. Has high adherence (as detected using self-report adherence questionnaire)

Design outcomes

Primary

MeasureTime frame
1. Usability and acceptability of the intervention from the viewpoint of community pharmacists using qualitative face-to-face interviews conducted following the completion of all patient appointments 2. Usability and acceptability of the intervention from the viewpoint of older patients using qualitative telephone interviews conducted after the patient has attended their final intervention appointment

Secondary

MeasureTime frame
1. Feasibility of the screening strategy (i.e. inclusion and exclusion criteria), recruitment strategy and willingness of participants to be recruited, assessed based on the numbers approached and those who are subsequently recruited 2. Feasibility of data collection procedures, assessed by collecting data on self-reported adherence and health-related quality of life via validated questionnaires, and collecting data from pharmacy-held Patient Medication Records to calculate objective measures of medication adherence such as Medication Possession Ratios 3. Fidelity to the intervention, assessed by examining materials (e.g. appointment check lists, summary notes) completed by pharmacists during the study. Pharmacists and patients are also asked about the delivery and receipt of components of the intervention, during qualitative feedback interviews

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 1, 2026