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Improving Medication Therapy Through a Digital Interdisciplinary Medicine Therapy Optimisation Model

Improving Medication Therapy and Patient Involvement Through a Digital Interdisciplinary Model Among Old People in Primary Care Living in Sparsely Populated Regions in Sweden

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05629936
Acronym
MTO
Enrollment
100
Registered
2022-11-29
Start date
2023-11-22
Completion date
2028-12-01
Last updated
2026-05-05

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

Conditions

Beliefs About Medicines, Health-related Quality of Life, Medication-related Problems, Self-reported Medication Adherence

Keywords

Telemedicine, Medication reconciliation, Clinical pharmacist, Adherence, Telepharmacy, Medication-related problems, Aged, Structured medication review

Brief summary

In this study, a telepharmacy service in primary care for home-living older adults in Northern Sweden's rural areas will be developed and evaluated. The primary objective is to evaluate the effect of the service regarding the identification, classification, and resolution of medication-related problems (MRPs). Secondary objectives are to evaluate participants' medication adherence, health-related quality of life, and beliefs about medicines through self-report questionnaires. The telepharmacy service include medication interviews, structured medication reviews, interdisciplinary patient-centred discussions, and follow-ups.

Detailed description

Participants that meet the inclusion criteria will be invited to participate in the study via mail. The participants will also receive three validated questionnaires; Medication Adherence Report Scale-5 (MARS-5), EuroQol-5 Dimension-5 Level questionnaire (EQ-5D-5L) and The Beliefs about Medicines Questionnaire (BMQ) to fill in prior to initiation of the study, to collect baseline data. The intervention consists of several steps, and all meetings will be conducted through video conferencing via a secure virtual care platform. Initially, the participant will have a medication interview with a clinical pharmacist, Next, the clinical pharmacist conducts a structured medication review based on information from the interview and the participant's medical records and laboratory values. The clinical pharmacist and the participant's primary care physician will then have a video-based interdisciplinary meeting. During this meeting, the clinical pharmacist presents recommendations to resolve potential MRPs, and the physician may accept or reject the pharmacist's recommendations. The primary-care physician informs the participant about any changes in their medication therapy and follows-up and monitors these changes. Video-based follow-up meetings between the participant and the clinical pharmacist will take place 1-2, 4 and 12 weeks after the first video-based meeting. Additional meetings can be scheduled, if requested by the participant, or if considered necessary by the clinical pharmacist. The clinical pharmacist will also conduct medical record reviews once every two weeks during the 12-week intervention period. At 12 weeks, after the last follow-up, the participant will be asked to fill in the three questionnaires one more time.

Interventions

OTHERTelepharmacy service

Video-based medication interviews, structured medication reviews, interdisciplinary patient-centred discussions, follow-ups

Sponsors

Umeå University
Lead SponsorOTHER
Region Västerbotten
CollaboratorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Using five or more prescribed medications and/or considered as a potential candidate by the primary care physician. * Living at home (i.e not in a nursing home) * Registered at primary healthcare centres in rural municipalities within Västerbotten County (and neighbouring counties if necessary)

Exclusion criteria

* Do not speak Swedish * Unable to communicate * Has a confirmed major neurocognitive disorder * Receives palliative care

Design outcomes

Primary

MeasureTime frameDescription
Identification and classfication of medication-related problemsThe 12-week intervention periodClassification of mediation-related problems according to a modified version of the classification system by Cipolle et al (1998).
Resolution of medication-related problems12-week intervention periodThe clinical pharmacists' recommendations to resolve medication-related problems will be classified according to a modified version of a system developed by the French Society of Clinical pharmacy. Physicians' acceptance rate of pharmacists' recommendations will be classified. The acceptance rate will be classified as accepted recommendation, rejected recommendation, or unknown.
Intra-individual change in self-reported medication adherence: Medication Adherence Report Scale-5 (MARS-5)Baseline and 12 weeksAssessing self-reported medication adherence through the MARS-5 questionnaire. Total score ranging between 5 and 25, with higher scores indicating a higher level of medication adherence.
Intra-individual change in self-reported health-related quality of life: EuroQol-5 Dimension-5 Level questionnaire (EQ-5D-5L)Baseline and 12 weeksAssessing health-related quality of life through the EQ-5D-5L-questionnaire. The questionnaire consists of five questions regarding self-perceived quality of life, and a visual analogue scale on which the respondents evaluate their own health status on a scale of 0-100.
Intra-individual change in self-reported beliefs about medicines: The Beliefs about Medicines Questionnaire (BMQ)Baseline and 12 weeksAssessing beliefs about medicines through the BMQ. The questionnaire consists of two different scales; BMQ-General assesses the respondent's beliefs about medicines in general and BMQ-Specific evaluates the individual's beliefs about medicines prescribed for their own use.

Countries

Sweden

Contacts

PRINCIPAL_INVESTIGATORMaria Gustafsson, Ph.D

Department of Medical and Translational Biology, Umeå University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 6, 2026