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Improving medication use with Balto

Balto: Improving medication adherence among people receiving cardiovascular risk management treatment using an integrated e-communication strategy - Balto

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON58033
Enrollment
400
Registered
2025-09-29
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

medication adherence

Interventions

Balto is a recently developed digital platform that provides patients with accessible, tailored information about their condition and prescribed medication, aiming to support medication adherence.

Sponsors

Obseq
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All people who started treatment for cardiovascular risk management within the last six months prior to the start of the study (extendable to twelve months if needed for recruitment), aged = 18 years, are eligible for inclusion. Eligible medication classes include antihypertensives (thiazide diuretics, ACE inhibitors, angiotensin receptor blockers, dihydropyridines, selective beta blockers), lipid-lowering medications (statins, ezetimibe), glucose-lowering medications, and antithrombotics. Only individuals who can understand and read Dutch, have a valid email address, and are able to create a digital account will be included.

Exclusion criteria

Exclusion criteria: Patients whose medication care has been transferred to nursing staff, such as in nursing homes, are excluded. Patients with contra-indication heart failure are excluded. Furthermore, patients using a medicine role are excluded.

Design outcomes

Primary

MeasureTime frame
Treatment adherence measured using the MARS-5 questionnaire at 9 months follow-up.

Secondary

MeasureTime frame
Treatment adherence, measured using the MARS-5 questionnaire at 3- and 6-months follow-up; Discontinuation of preventive cardiovascular medication, as reported by the patient, at 3-, 6-, and 9-months follow-up. Relevant cardiovascular risk parameters; Number of contact moments with pharmacy or general practice staff, as reported by the patient; Perceived health and satisfaction with received information: questionnaires; Attitudes towards Balto platform; Intervention engagement. 

Countries

Netherlands

Contacts

Public ContactK Taxis

Obseq

k.taxis@rug.nl06 29510316

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)