Supporting Patients Starting New Medicines: Evaluating the myCare Start Service in Switzerland
Launched by UNIVERSITY OF GENEVA, SWITZERLAND · Jun 16, 2025
Trial Information
Current as of July 05, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at a new support service called myCare Start, designed to help people in Switzerland who are starting new long-term medicines for conditions like heart disease, diabetes, depression, asthma, and COPD (a lung disease). The goal is to see if this service helps patients take their medicines correctly, if it’s cost-effective, and how well it works when used in everyday medical and pharmacy settings. This could help make sure the service is available and funded for patients in the future.
People who might join this study are adults aged 65 and older with basic health insurance in Switzerland, who have just been prescribed a new medicine for one of these chronic conditions. To participate, they need to manage their own medications at home, understand the local language (French, German, or English), and agree to share some health information. If they join, patients in the study will receive support from pharmacists trained in the myCare Start service, who will help them understand their new medicines and how to take them properly. The study is not yet recruiting, but it aims to make starting new treatments easier and safer for patients managing long-term health conditions.
Gender
ALL
Eligibility criteria
- • Patients
- Inclusion Criteria:
- • Must have mandatory basic health insurance in Switzerland
- • Must have been newly prescribed one or more new long-term medications in accordance with the following chronic conditions: cadisovascular diseases (incl. hyertension and thromboprophylaxis), diabetes, hyperlipidemia, depression, respiratory illness (asthma and COPD)
- • Must be 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)
- • Must be able to understand language spoken by pharmacy staff and can read and understand study documents (French, German, English)
- • Must understand and are willing to consent to the myCare Start-I study (including the agreement on self-reported questionnaires and collection of health care data via their health insurance company)
- • in the intervention arm, patients must receive the myCare Start service
- For this study, 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. Included in this working definition:
- • The new medication is indicated for one of the five long-term diseases listed above
- • Patient has never had this active ingredient dispensed before (patient still considered eligible if they have received a small initial sample pack from their physician) or restarts an active ingredient after a period of interruption of at least 12 months (time period to be reported by the patient). Please note that for patients, that have already started a sample pack of medication the myCare Start Consultation One can start upon first dispensation at the pharmacy, there is no need to wait 7-14 days.
- • 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 of inhalators for asthma/COPD)
- • Intensification of dosage regiment (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 1000 mg 1-0-0 instead of 500 mg 1-0-1; change in antihypertensive drug regiment in elderly patients having vertigo in the morning: 0-0-X instead of X-0-0)
- 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)
- Physicians:
- • Inclusion criteria
- • - Any physician treating a patient for one of the five long-term illnesses listed above is eligible to refer the patient to a pharmacy providing myCare start.
- Pharmacies:
- Inclusion criteria:
- • Have to be enrolled into the myCare Start service and comply to the requirements of the pharmacy quality system management of having access to a private consultation room or area
- • Must agree to participate in the research study, including the recruitment of control patients and the delivery of the myCare Start service to intervention patients.
About University Of Geneva, Switzerland
The University of Geneva, located in Switzerland, is a prestigious research institution renowned for its commitment to advancing scientific knowledge and improving public health. With a strong emphasis on interdisciplinary collaboration, the university conducts cutting-edge clinical trials aimed at exploring innovative therapies and enhancing patient care. Its dedicated research teams, equipped with state-of-the-art facilities and a robust ethical framework, strive to translate scientific discoveries into practical applications, ultimately contributing to the global advancement of medical science and the well-being of diverse populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Geneva, , Switzerland
Patients applied
Trial Officials
Marie Paule Schneider, Prof. PhD
Principal Investigator
Uinversity of Geneva
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported