Status:

ACTIVE_NOT_RECRUITING

Implementation of a New Model of Care for Supporting Long-term Medication Adherence (Phase A)

Lead Sponsor:

University of Geneva, Switzerland

Collaborating Sponsors:

University of Basel

Fundació Sant Joan de Déu

Conditions:

Medication Initiation for Long-term Conditions

Eligibility:

All Genders

18+ years

Brief Summary

The overall objective of the myCare Start-I project is to adapt, implement and evaluate the myCare Start service within the Swiss pharmacy-physician network to enhance medication adherence during the ...

Detailed Description

Phase A: 1. To conduct a contextual analysis of the current Swiss primary care ecosystem as related to pharmacy-physician interprofessional health services for patients with long-term diseases (i.e.,...

Eligibility Criteria

Inclusion

  • Phase A: contextual analysis
  • Community pharmacists and technicians of 5 participating pharmacies in the French-speaking part of Switzerland and 5 in the German-speaking part of Switzerland
  • Primary care physicians working in collaboration or in the neighbourhood of the participating pharmacies
  • Patients with long-term treatments, who are a regular patients of the included pharmacies
  • International research groups who have implemented NMS within their countries or similar interventions.

Exclusion

  • Patients not willing to participate
  • Patients that do not speak French or German
  • Phase B: hybrid type 2 effectiveness-implementation study
  • Patients are eligible for the myCare Start-I phase B study if :
  • They are taking part in the myCare Start service
  • They have been newly prescribed one or more new long-term medications in accordance with one of the five defined long-term conditions (cardiovascular disease (incl. hypertension and thromboprophylaxis), diabetes, hyperlipidaemia, depression and respiratory illness (asthma, COPD))
  • They are 18 years or older
  • They have mandatory basic health insurance in Switzerland
  • They are able to self-manage treatment (i.e. they live at home without any support to manage their medication, exception: patient uses a pill dispenser and fills it in by him-/herself).
  • They understand language spoken by pharmacy staff and are able to read and understand study documents (ge, fr)
  • They are able to understand and willing to consent to the myCare Start study (including the agreement on self-reported questionnaires and collection of health care data via their health insurance company)
  • Exclusion criteria:
  • • Patients participating or having participated in an education program about their disease or treatment in the last 3 months, led by healthcare providers such as physicians, nurses, pharmacists or other (e.g. education provided by nurses for type I diabetes patients).
  • myCare Start definition of a new medication:
  • A new medication is a medication that has not been previously dispensed to the patient. This includes one or more new medications for a new diagnosis and or new medications for pre-existing diagnosis of a long-term condition.
  • Operational definition of a new medication:
  • Active ingredient is indicated for one of the five long-term conditions (cardiovascular disease (incl. hypertension and thromboprophylaxis), diabetes, hyperlipidaemia, depression and respiratory illness (asthma, COPD)).
  • Patient has never had this active ingredient dispensed before or restarts an active ingredient after a period of interruption of at least 12 months.
  • The new active ingredient can be part of a combo preparation (e.g. a diuretic added to an ACE inhibitor into the same preparation)
  • Patient has had no change in active ingredient but has an important change in treatment administration, such as:
  • Change of galenic form (e.g. two different types on inhalators for asthma/COPD)
  • Intensification of dosage regimen (e.g. twice a day instead of once a day)
  • The following change is not considered as medication initiation:
  • New dosage of already known active ingredient (e.g. dose escalation of antidepressants)
  • Simplification of administration mode (e.g. metformin 1000mg 1-0-0 instead of 500mg 1-0-1; change in antihypertensive drug regimen in elderly patients having vertigo in the morning: 0-0-X instead of X-0-0)

Key Trial Info

Start Date :

August 30 2023

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

June 30 2026

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT06191835

Start Date

August 30 2023

End Date

June 30 2026

Last Update

April 18 2025

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Université de Genève

Geneva, Canton of Geneva, Switzerland, 1211

2

University of Basel

Basel, Switzerland, 4056