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Clinical Trials/NCT06016140
NCT06016140
Completed
Not Applicable

Applying a Medication Plan for Safer Medication Treatment in Older Persons - a Feasibility Study

Region Jönköping County1 site in 1 country30 target enrollmentJune 1, 2022
ConditionsPatient Safety

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patient Safety
Sponsor
Region Jönköping County
Enrollment
30
Locations
1
Primary Endpoint
Feasibility of the intervention
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Harm from medications is still a concern in an aged population. As medication treatment for older persons many times are complex, a feasibility study can be helpful to support decisions about future evaluation and implementation of an intervention.

In this study, the overall aim is to assess feasibility, acceptability and potential effects of usage of a co-designed medication plan for older persons with medication treatment.

The study will take place in the primary care setting in Sweden, and involve persons 75 years or older using five or more medications on daily basis, physicians at primary care centers and persons supporting the older person in their medication use a home.

During an appointment, the physician and older person will agree on a medication plan, that will be documented in the older person's electronic health record and printed out on paper.

After three month, the potential outcomes of a medication plan will be collected, together with data about feasibility and acceptability of the intervention. Two questionnaires will be used, addressing usability and patient safety. Moreover, remote interviews with participants will be performed to address usability and patient safety. Information about the medication plan will be collected from the electronic health record. Data analysis will be done with descriptive statistics and qualitative content analysis.

Expected outcomes are an assessment of feasibility and acceptability, and potential outcomes, to support decision on a future evaluation of the medication plan.

Registry
clinicaltrials.gov
Start Date
June 1, 2022
End Date
November 1, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Region Jönköping County
Responsible Party
Principal Investigator
Principal Investigator

Malin Holmqvist

PhD student, pharmacist

Region Jönköping County

Eligibility Criteria

Inclusion Criteria

  • Physicians and nurses: regular contact with the older person regarding medications, employment at a primary care center and ability to understand and communicate in Swedish
  • Older persons: age \>75 years old, five or more medications on a regular basis and ability to understand and communicate in Swedish
  • Next-of-kin: age \> 18 years old, regular contact with the older person regarding medications, ability to understand and communicate in Swedish

Exclusion Criteria

  • Older persons: impaired cognitive ability affecting the ability to provide informed consent (Diagnosis code for dementia) and late palliative phase, here defined as estimated life expectancy shorter than six months
  • Next-of-kin: impaired cognitive ability affecting the ability to provide informed consent

Outcomes

Primary Outcomes

Feasibility of the intervention

Time Frame: Three months

For feasibility of the intervention, the secondary outcome measures will be analyzed together to address the feasibility of chosen study methods and of the intervention of using a co-designed medication plan

Secondary Outcomes

  • Patient safety(Three months)
  • Usability of the medication plan(Three months)
  • Acceptability of the intervention(Three months)
  • Healthcare utilisation(Three months)

Study Sites (1)

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