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Opti-Med: Optimisation of a medication review programme for elderly in general practice.

The effectiveness of an optimized medication review programme in patients with ‘geriatric giants’ in general practice.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29548
Enrollment
500
Registered
2013-11-12
Start date
2013-11-13
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Elderly of 65 years and older with geriatric giant problems Dutch: Ouderen van 65 jaar of ouder met geriatrische reuzen problematiek

Interventions

Intervention group An external expert team consisting of an assistant, a general practitioner and a pharmacist will carry out the medication review of every participating patient in the intervention

Sponsors

VU Medical Center and NIVEL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: One or more of the following new geriatric giants: 1. Actual mobility problem; 2. Two falls or more in the last 6 months; 3. One fall in the last 6 months and a score on the visual analogue scale for Fear of Falling (VAS-FOF) of 5 or more; 4. Dizziness; 5. Urinary incontinence; 6. Problems with cognition. The geriatric giants identification is a two-step approach: 1. Identification by ICPC codes in GP registration system. Every 8 weeks patients who consulted the GP with a relevant diagnosis in this time period and did not present the problem to the GP during the previous 12 months will be invited to participate. 2. Self-report by patients of the presence of at least one geriatric giant (5 or more on a scale of 1-10) Additionally they have to indicate that they are willing to participate in the trial by signing an informed consent form.

Exclusion criteria

Exclusion criteria: - All patients with a diagnosis of dementia in the medical record. - Patients with an MMSE score of 18 or less. An MMSE interview is only carried out when patients indicated they needed help to fill in the inclusion questionnaire. - A terminal illness leading to an expected death within six months. - Not willing or unable to participate in studies trials according to GPs. - Received a systematic medication review according to polypharmacy Dutch guidelines in the last 6 months

Design outcomes

Primary

MeasureTime frame
1. Quality of Life as assessed with EQ5D and SF12 by the patient and with the EQ5D by proxies. 2. The presence of geriatric giants on a scale from 1-10.

Secondary

MeasureTime frame
- Number of drug related problems - Medication satisfaction - Medication adherence - Cost effectiveness - Surplus value of the patient participation on the outcome of the medication advice - Follow-up of the medication advice by GP and patient - Process analysis on succes and failure factors

Contacts

Public ContactFloor Willeboordse

Van der Boechorstraat 7, room D550

f.willeboordse@vumc.nl+31-(0)20-4445584

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)