Towards the development of a personalised E-Health intervention for use in community pharmacies to analyse and improve medication non-adherence in people with type 2 diabetes mellitus, who are non-adherent to oral blood glucose and/or blood pressure lowering drugs.
Completed
- Conditions
- 10018424diabetesType 2 diabetes mellitus
- Registration Number
- NL-OMON55758
- Lead Sponsor
- Vrije Universiteit Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
- People with type 2 diabetes mellitus that are non-adherent to oral blood
glucose and/or bloodpressure lowering drugs.
- Participants aged 35-75 years.
- Mobile phone user.
Exclusion Criteria
- People in which adherence data is invalid for instance due to hospital
admission.
- People that use medication-intake supporting pill packaging services provided
by the pharmacy.
- People that suffer from major psychiatric disorders.
- People that are *starters*, meaning that they started using the medicine
somewhere in the period in which the dispensing score was calculated.
- People that are *stoppers*, meaning that they did not have a medicine
dispatch in the last four months of the period in which the dispensing score
was calculated.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary study outcome is medication adherence (measured with change in a<br /><br>telephone pill count). </p><br>
- Secondary Outcome Measures
Name Time Method <p>The secondary study parameters are:<br /><br>- Systolic blood pressure (registry data)<br /><br>- HbA1c (registry data)<br /><br>- Medication adherence (MARS-5 questionnaire)<br /><br>- Attitude and beliefs toward medication (BMQ specific questionnaire)<br /><br>- Satisfaction with diabetes treatment (DTSQs+c questionnaire)<br /><br>- Quality of life (EQ-5D-5L questionnaire)<br /><br>- Medical and productivity costs (iMTA costs questionnaire)<br /><br><br /><br>The other study parameters are:<br /><br>- Barriers and facilitators that people with type 2 diabetes and pharmacists<br /><br>experience in the use of the intervention.<br /><br>- Refinement of the non-adherence profiling algorithm after evaluation of the<br /><br>intervention. </p><br>