Alzheimer's Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
For patients and their caregivers:
- The patient has been diagnosed with both mild cognitive impairment or Alzheimer's disease/related dementia, and diabetes
- The patient currently has active prescriptions for diabetes treatment
- The patient has attended at least one appointment at an Eskenazi or IU Health primary care clinic within the past 12 months
- If the patient is unable to consent for themselves, they must be able to give assent and have a legally authorised representative who can consent on their behalf
- The patient has a caregiver who is 18 years of age or older and spends time with the patient every day, or nearly every day
- Both the patient and caregiver speak English
- Both the patient and caregiver live in the community (not in a care facility)
- The patient and caregiver have access to the internet
For healthcare providers (a separate part of the trial):
- Eligible clinician types include primary care doctors, nurses, pharmacists, nutritionists, psychologists, and medical residents
Who may not be able to join:
For patients and their caregivers:
- The patient has a terminal illness
- The patient uses an automated insulin delivery system
- The patient is currently receiving dialysis
- The patient is taking vitamin C (ascorbic acid) during the monitoring period
- The patient has an implanted medical device
- The patient has a bleeding disorder
- The patient has existing skin lesions on their arms
- The patient has an allergy to medical adhesive or isopropyl alcohol
- The patient has plans to undergo imaging or diathermy (a type of heat-based therapy) during the study period
For healthcare providers:
- Clinicians who only treat patients under the age of 65
- Clinicians who are not involved in managing patients' diabetes
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: April Savoy, PhD, Indiana University
Phone: 317-278-2194
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Feasibility- Recruitment; Feasibility- Retention; Feasibility- CGM Device Adherence; System Usability Scale; CollaboRATE Questionnaire; Number of Changes in Diabetes Management
Can't join this trial?
Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.