mGlide-Care: A Partnership With Caregivers

Not Applicable

Not yet recruiting

• Conditions: HTN
• Interventions: Other: mGlide-Care; Other: Usual Care +

• Registration Number: NCT05850416
• Lead Sponsor: University of Minnesota

Brief Summary

Hypertension (HTN) is the most significant stroke, cardiovascular disease and dementia risk factor and is substantially under-treated especially in older persons. In this study the investigators will develop mGlide-Care to address uncontrolled HTN in people with mild cognitive impairment (MCI) and early stage Alzheimer's Disease and Alzheimer's Disease Related Dementia (AD/ADRD). mGlide-Care is adapted from mGlide which is a mHealth (mobile health technology) mediated care model for HTN care. Aim 1 will engage stakeholders to study the acceptability of mHealth mediated HTN care and will use their input to develop mGlide-Care. Stakeholders are persons with early stage AD/ADRD and MCI, unpaid family caregivers, primary care providers, geriatricians and clinical pharmacists. Aim 2 is a feasibility pilot to test mGlide-Care vs. usual care in 75 participants with uncontrolled HTN and early stage AD/ADRD or MCI. Caregivers will assist participants. Outcomes will include HTN control and participant and caregiver reported measures.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2023-03-24
• Study First Submitted QC: 2023-04-28
• Study First Posted: 2023-05-09
• Status Verified: 2025-04
• Last Update Submitted: 2025-04-03
• Last Update Posted: 2025-04-04
• Study Start: 2025-06
• Primary Completion: 2028-05-30
• Study Completion: 2028-05-30

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 75

Inclusion Criteria

Must meet all criteria

• Diagnosed with early stage AD/ADRD or MCI
• Have uncontrolled hypertension (HTN)
• Have an unpaid, family caregiver
• Have established medical diagnosis of hypertension (HTN)
• English speaking
• Participant or caregiver must have a smartphone or mobile device (e.g. iPad) that can transmit blood pressure (BP) from the BP monitor
• Participant and caregiver capable and willing to comply with the entire study protocol
• Able to give voluntary written informed consent.

Exclusion Criteria

Any of the following will be an exclusion.

• Severe comorbid illness including end-stage kidney disease, end-stage liver disease, and life expectancy <1 year, or if medical complexity of the patient precludes clinical trial participation
• Active illicit drug use (e.g. cocaine, methamphetamines, opioids, phencyclidine) since this will interfere with HTN management
• Participant and caregiver unable to complete study tasks, including are homeless, will leave the country, or will relocate in the next 12 months
• Serious psychiatric illness that could interfere with treatment, assessment, or compliance including significant delusional disorders such as schizophrenia and bipolar illness
• Unable or unwilling to give consent.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
mGlide-Care	mGlide-Care	mHealth mediated HTN care model with self-monitoring and medication adjustment
Usual Care Plus	Usual Care +	Usual Care including self-monitoring support

Primary Outcome Measures

Name	Time	Method
HTN control	6 months and 12 months	HTN control rates in intervention vs. control arm participants. HTN control for each participant will be defined based on personalized threshold for participant as determined by primary care.