This project will provide new evidence on how to optimize medication use among older people with limited life expectancy. This will be done by testing whether a patient-centered deprescribing intervention, focused on aligning medical treatment with patients' preferences, can improve quality of life among older people with limited life expectancy.
In a pragmatic randomized controlled trial, this project will test whether a comprehensive and patient-centered deprescribing intervention can improve quality of life among older people with limited life expectancy. The intervention will comprise a series of consultations between the patient and general practitioner (GP) (at least three) to continuously adjust the patient's medication according to the patient's goals, needs, and preferences, thereby ensuring alignment with the patient's priorities. Thus, the purpose of this intervention is to initiate and facilitate a continued deprescribing process. The process can be summarized in eight steps: During an initial consultation (1: Consultation 0), the GP assesses patient eligibility. If the patient would like to participate, a project nurse subsequently visits the patient at home (2: Home visit) for retrieval of informed consent as well as baseline measurements. After retrieval of informed consent, patients are randomized. Patients randomized to the control group continue with usual care (consultations with their GP when needed). Patients in the intervention group receive the intervention, comprising a series of consultations between the patient and GP (at least three). During the first intervention consultation (3: Consultation 1), the patient and GP discuss how the patient feels about their medical treatment, and the GP provides the patient with written material for the patient to prepare prior to the next consultation. The patients prepare (4: Preparation) by considering and verbalizing their goals of care and treatment preferences. Simultaneously, a clinical pharmacist examines the patient's medication list and provides suggestions to the GP on which drugs can be continued and deprescribed, respectively. During the next intervention consultation (5: Consultation 2), the patient and GP discuss the patient's preferences and initiate deprescribing initiatives aligned with the patient's priorities. During a new intervention consultation (6: Consultation 3), the patient and GP follow up on the changes initiated and initiate new deprescribing initiatives if such can be identified. If needed, subsequent intervention consultations (7: Consultation X) are planned until the patient and GP consider the patient's medical treatment optimal. A project nurse visits all patients (both patients randomized to the control and intervention group, respectively) at home 3 and 6 months after first home visit to retrieve follow-up measurements (8: Follow-ups). A project nurse retrieves medication lists at 3 months, 6 months, and 12 months.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Enrollment
188
The intervention is comprised of a minimum of three consultations with a general practitioner (GP), where adjustment of the patient's medication is made according to the patient's preference, goals and needs Consultation 1: Patient and GP discuss how the patient feels about their medical treatment, and the GP provides the patient with written material for the patient to prepare prior to the next consultation. Consultation 2: A clinical pharmacist have beforehand examined the patient's medication list and provided suggestions to the GP on which drugs can be deprescribed. The patient and GP discuss the patient's preferences and initiate deprescribing initiatives aligned with the patient's priorities. Consultation 3: Patient and GP follow up on the changes initiated and initiate new deprescribing initiatives if such can be identified. If needed, subsequent consultations (Consultation X) are planned until the patient and GP consider the patient's medical treatment optimal.
Odense University Hospital
Odense, Region Syddanmark, Denmark
HEALTH-RELATED QUALITY OF LIFE
Health-related quality of life will be measured using the Danish version of the Short Form 12 Health Survey Version 2 (SF-12v2).
Time frame: Baseline
CHANGE FROM BASLINE HEALTH-RELATED QUALITY OF LIFE AT 3 MONTHS
Health-related quality of life will be measured using the Danish version of the Short Form 12 Health Survey Version 2 (SF-12v2).
Time frame: 3 months
CHANGE FROM BASLINE HEALTH-RELATED QUALITY OF LIFE AT 6 MONTHS
Health-related quality of life will be measured using the Danish version of the Short Form 12 Health Survey Version 2 (SF-12v2).
Time frame: 6 months
HEALTH-RELATED QUALITY OF LIFE (DEPRESSION)
Health-related quality of life will be measured using the Danish version of the Depression List (DL).
Time frame: Baseline
CHANGE FROM BASLINE HEALTH-RELATED QUALITY OF LIFE (DEPRESSION) AT 3 MONTHS
Health-related quality of life will be measured using the Danish version of the Depression List (DL).
Time frame: 3 months
CHANGE FROM BASLINE HEALTH-RELATED QUALITY OF LIFE (DEPRESSION) AT 6 MONTHS
Health-related quality of life will be measured using the Danish version of the Depression List (DL).
Time frame: 6 months
MORTALITY
Mortality will be assessed through the nationwide Danish Central Person Registry (CPR).
Time frame: 3 months
MORTALITY
Mortality will be assessed through the nationwide Danish Central Person Registry (CPR).
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Time frame: 6 months
MORTALITY
Mortality will be assessed through the nationwide Danish Central Person Registry (CPR).
Time frame: 12 months
COGNITIVE FUNCTION
Cognitive function will be measured using the Danish version of the Mini-Mental State Examination Version 2 Standard Form (MMSE-2).
Time frame: Baseline, 3 months and 6 months
FUNCTIONAL LEVEL
Functional level will be measured using the Danish version of the Vulnerable Elders Survey 13 (VES-13).
Time frame: Baseline, 3 months and 6 months
HAND-GRIP STRENGTH
Hand-grip strength will be measured using a hand-grip dynamometer.
Time frame: Baseline, 3 months and 6 months
NUMBER OF MEDICATION DISCONTINUED
Number of medications discontinued will be assessed through the medication lists.
Time frame: 3 months, 6 months and 12 months
NUMBER OF MEDICATION CHANGES
Number of medication changes will be assessed through the medication lists.
Time frame: 3 months, 6 months and 12 months
HOSPITAL ADMISSIONS
Hospital admissions will be assessed through the nationwide Danish National Patient Registry.
Time frame: 3 months, 6 months and 12 months
HEALTH CARE COSTS
Health care costs will be assessed through nationwide Danish Health Care registries.
Time frame: 3 months, 6 months and 12 months
SUCCESS RATE OF THE INTERVENTION
Success rate will be assessed through persisting discontinuations and changes of medications via the medication lists.
Time frame: 3 months, 6 months and 12 months