STAPP: Improving Adherence to Statin Therapy Through a Medication Management Application

Sponsor
University Hospital, Essen (Other)
Overall Status
Recruiting
CT.gov ID
NCT05777655
Collaborator
(none)
250
1
2
48.4
5.2

Study Details

Study Description

Brief Summary

Interventional study to compare standard of care vs standard of care plus the use of a medication therapy management smartphone app (mediteo m+, Mediteo GmbH, Heidelberg) in patients with atherosclerotic cardiovascular disease and indication to start high intensity statin therapy.

Condition or Disease Intervention/Treatment Phase
  • Other: Medication management app (mediteo m+, Mediteo GmbH, Heidelberg)
N/A

Detailed Description

Patients with atherosclerotic cardiovascular disease and indication to start high intensity statin therapy will be recruited during hospital-stay or in the neurovascular outpatient clinic of the Neurology Department as well as in the Department of Cardiology and Vascular Medicine at the University Hospital Essen. Participants will be randomly allocated 1:1 to the intervention or control arm and all will receive a Low density Lipoprotein-Cholesterin (LDL-C) target and a statin-prescription as standard of care. All patients will be asked to take the prescribed statin in the evening and to provide LDL-C values measured by the family physician after 6 and 18 months. Additional blood will be collected after 6 and 18 months to control for cardiovascular risk-factors in the study center (LDL-C amongst others). In addition, the intervention group will receive free access to a study version of the medication management app mediteo m+ (Mediteo GmbH, Heidelberg). Installation of the app will be performed on the day of enrolment. After entering the medication, the app will remind the patient to take his or her statin therapy according to the therapy plan. Each intake has to be confirmed by the patient, either directly via the reminder notification or in the app. In addition, the app can be used to set reminders to go the family physician to take LDL-C values and to document the personal LDL-C values. The endpoint assessment will be performed in blinded manner.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
250 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
Improving Adherence to Statin Therapy Through a Medication Management Application (STAPP)
Actual Study Start Date :
Feb 17, 2023
Anticipated Primary Completion Date :
Feb 28, 2025
Anticipated Study Completion Date :
Feb 28, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Medication management app

Standard of care (statin prescription, targeted monitoring of individual LDL-C values by primary care physician) + medication management app and follow-up visits at our institution at 6 and 18 months

Other: Medication management app (mediteo m+, Mediteo GmbH, Heidelberg)
Free access to a study version of the medication management app mediteo m+ for reminders and documentation of statin therapy in addition to usual care

No Intervention: Standard of care

Statin prescription, targeted monitoring of individual LDL-C values by primary care physician and follow-up visits at our institution at 6 and 18 months

Outcome Measures

Primary Outcome Measures

  1. Relative change in LDL-C [6 months]

    Relative change in LDL-C (mg/dl) after 6 months measured by study site (or according to the value measured by the family physician, if the value measured by the study site is not available after 6 months) as compared to baseline-value

Secondary Outcome Measures

  1. Modified Rankin Scale (mRS)-Score after 6 months [6 months]

    Change in mRS [0 to 6, higher scores indicating worse outcome] after 6 months

  2. Proportion of available LDL-C values measured by the family physician after 6 months [6 months]

    Proportion of available LDL-C values measured by the family physician after 6 months

  3. Relative change in high density lipoprotein-cholesterol (HDL-C) after 6 months [6 months]

    Relative change in HDL-C (mg/dl) after 6 months as compared to baseline-value

  4. Relative change in total cholesterol after 6 months [6 months]

    Relative change in total cholesterol (mg/dl) after 6 months as compared to baseline-value

  5. Relative change in hemoglobin A1C (HbA1c) after 6 months [6 months]

    Relative change in HbA1c (%) after 6 months as compared to baseline-value

  6. Relative change in high-sensitivity C-reactive protein (hsCRP) after 6 months [6 months]

    Relative change in hsCRP (mg/dl) after 6 months as compared to baseline-value

  7. Relative change in Lipoprotein (a) after 6 months [6 months]

    Relative change in Lipoprotein (a) (mg/dl) after 6 months as compared to baseline-value

  8. Relative change in glutamic oxaloacetic transaminase (GOT) after 6 months [6 months]

    Relative change in GOT (U/l) after 6 months as compared to baseline-value

  9. Relative change in glutamate-pyruvate transaminase (GPT) [6 months]

    Relative change in GPT (U/l) after 6 months as compared to baseline-value

  10. Relative change in creatine kinase (CK) after 6 months [6 months]

    Relative change in CK (U/l) after 6 months as compared to baseline-value

  11. Adherence to statin therapy as measured by the German version of the Medication Adherence Report Scale (MARS-D) after 6 months [6 months]

    Adherence to statin therapy after 6 months as measured by the German version of the Medication Adherence Report Scale as measured by MARS-D, range 5-25, higher scores indicating better adherence

  12. Adherence to statin therapy as measured by the German version of the A14 scale after 6 months [6 months]

    Measured by the German version of the A14 scale, range 0 - 56, lower scores indicating better adherence

  13. Change in Quality of life score EQ-5D-5L after 6 months [6 months]

    Change in Quality of life score EQ-5D-5L is a standardised measure of health status developed by the EuroQol Group including 5 dimensions, 5 levels and the EQ visual analogue scale [VAS] from 0 to 100 with higher values indicating higher quality of life

  14. Change in Beliefs about Medicines Questionnaire (BMQ) after 6 months [6 months]

    The BMQ consists of two sections assessing personal beliefs about the necessity of prescribed medication (5 items) and concerns (5 items). Scores range from 5 to 25 with higher scores indicating a higher degree of necessity/concern.

  15. Incidence of major vascular events after 6 months [6 months]

    Incidence of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina or urgent coronary revascularization therapy after 6 months

  16. Change in highest degree of extracranial stenosis after 6 months [6 months]

    Change in highest degree of extracranial stenosis (%) as determined by carotid ultrasound using North American Carotid Endarterectomy Trial (NASCET) criteria after 6 months

  17. Change in maximum height of largest carotid plaque after 6 months [6 months]

    Change in maximum height of largest carotid plaque (mm) on carotid ultrasound after 6 months

  18. Change in longitudinal area of largest carotid plaque after 6 months [6 months]

    Change in longitudinal area of largest carotid plaque [mm2] on carotid ultrasound after 6 months

  19. Change in cross-sectional area of largest carotid plaque after 6 months [6 months]

    Change in cross-sectional area of largest carotid plaque [mm2] on carotid ultrasound after 6 months

  20. Relative change in LDL-C after 18 months [18 months]

    Relative change in LDL-C (mg/dl) after 18 months measured by study site (or according to the value measured by the family physician, if the value measured by the study site is not available) as compared to baseline-value

  21. Modified Rankin Scale (mRS)-Score after 18 months [18 months]

    Change in mRS [0 to 6, higher scores indicating worse outcome] after 18 months

  22. Proportion of available LDL-C values measured by the family physician after 18 months [18 months]

    Proportion of available LDL-C values measured by the family physician after 18 months

  23. Relative change in high density lipoprotein-cholesterol (HDL-C) after 18 months [18 months]

    Relative change in HDL-C (mg/dl) after 18 months as compared to baseline-value

  24. Relative change in total cholesterol after 18 months [18 months]

    Relative change in total cholesterol (mg/dl) after 18 months as compared to baseline-value

  25. Relative change in hemoglobin A1C (HbA1c) after 18 months [18 months]

    Relative change in HbA1c (%) after 18 months as compared to baseline-value

  26. Relative change in high-sensitivity C-reactive protein (hsCRP) after 18 months [18 months]

    Relative change in hsCRP (mg/dl) after 18 months as compared to baseline-value

  27. Relative change in Lipoprotein (a) after 18 months [18 months]

    Relative change in Lipoprotein (a) (mg/dl) after 18 months as compared to baseline-value

  28. Relative change in glutamic oxaloacetic transaminase (GOT) after 18 months [18 months]

    Relative change in GOT (U/l) after 18 months as compared to baseline-value

  29. Relative change in glutamate-pyruvate transaminase (GPT) after 18 months [18 months]

    Relative change in GPT (U/l) after18 months as compared to baseline-value

  30. Relative change in creatine kinase (CK) after 18 months [18 months]

    Relative change in CK (U/l) after 18 months as compared to baseline-value

  31. Adherence to statin therapy as measured by the German version of the Medication Adherence Report Scale (MARS-D) after 18 months [18 months]

    Adherence to statin therapy after 18 months as measured by the German version of the Medication Adherence Report Scale as measured by MARS-D, range 5-25, higher scores indicating better adherence

  32. Adherence to statin therapy as measured by the German version of the A14 scale after 18 months [18 months]

    Measured by the German version of the A14 scale, range 0 - 56, lower scores indicating better adherence

  33. Change in Quality of life score EQ-5D-5L after 18 months [18 months]

    Change in Quality of life score EQ-5D-5L is a standardised measure of health status developed by the EuroQol Group including 5 dimensions, 5 levels and the EQ visual analogue scale [VAS] from 0 to 100 with higher values indicating higher quality of life

  34. Change in Beliefs about Medicines Questionnaire (BMQ) after 18 months [18 months]

    The BMQ consists of two sections assessing personal beliefs about the necessity of prescribed medication (5 items) and concerns (5 items). Scores range from 5 to 25 with higher scores indicating a higher degree of necessity/concern.

  35. Incidence of major vascular events after 18 months [18 months]

    Incidence of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina or urgent coronary revascularization therapy after 18 months

  36. Change in highest degree of extracranial stenosis after 18 months [18 months]

    Change in highest degree of extracranial stenosis (%) as determined by carotid ultrasound using North American Carotid Endarterectomy Trial (NASCET) criteria after 18 months

  37. Change in maximum height of largest carotid plaque after 18 months [18 months]

    Change in maximum height of largest carotid plaque (mm) on carotid ultrasound after 18 months

  38. Change in longitudinal area of largest carotid plaque after 18 months [18 months]

    Change in longitudinal area of largest carotid plaque [mm2] on carotid ultrasound after 18 months

  39. Change in cross-sectional area of largest carotid plaque after 18 months [18 months]

    Change in cross-sectional area of largest carotid plaque [mm2] on carotid ultrasound after 18 months

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age >18 years

  • Atherosclerosis (neurovascular, cardiac or peripheral) with an indication to start a high intensity statin-therapy (equivalent to 40mg of atorvastatin or 20mg of rosuvastatin; start of statin therapy +/- 10 days of enrolment)

  • Statin naivety

  • LDL-C >100 mg/dl. No older than 21 days

Exclusion Criteria:
  • Inability to take medication independently or to use the mediteo m+ app independently (e.g. people in need of care, people with dementia)

  • Patient has no own smartphone (no device provided for this study)

  • Prior drug therapy to lower LDL-C within the last 30 days

  • Active cancer (defined as a diagnosis of cancer within 6 months before enrolment, any treatment for cancer within the previous 6 months, or recurrent or metastatic cancer) or other severe concomitant disease with a life expectancy of <6 months

  • Use of a digital therapy management application (including mediteo or mediteo m+) within the last month

  • Participation in another interventional trial

  • Pregnancy

  • Inability or unwillingness to provide informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital, Essen Essen Nordrhein-Westfalen Germany 45147

Sponsors and Collaborators

  • University Hospital, Essen

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Benedikt Frank, Assistant Professor (PD) Dr. med, University Hospital, Essen
ClinicalTrials.gov Identifier:
NCT05777655
Other Study ID Numbers:
  • 21-10444
First Posted:
Mar 21, 2023
Last Update Posted:
Mar 21, 2023
Last Verified:
Mar 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Benedikt Frank, Assistant Professor (PD) Dr. med, University Hospital, Essen
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 21, 2023