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Not yet recruiting NCT07659548

Home-based Monitoring & Enabled Medication Independence With New Digital Tools

No phase Interventional Older Adults (65 Years and Older) Living Alone Mild Cognitive Decline Polypharmacy (People Under Treatment With 5 or More Drugs)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: HOME-MIND.
Who it may be relevant to
Registry conditions: Older Adults (65 Years and Older), Living Alone, Mild Cognitive Decline, Polypharmacy (People Under Treatment With 5 or More Drugs). Basic parameters: from 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Technological Innovation to Support Medication Safety and Optimization in Older Adults Living Alone With Cognitive Decline

Overview

This clinical trial is studying an online tool that may help older adults safely manage their medications at home. The study focuses on older adults who live alone and have memory concerns or mild changes in thinking. Many people in this group take several medications, which can make it hard to keep track of when and how to take them, notice side effects, or know when to ask for help. In this study, participants use an online self-monitoring platform to record any problems, symptoms, or concerns they have while taking their medications. The platform also provides helpful education and suggestions for managing medications and symptoms. Participants can share summaries from the platform with their health care team, which may help improve communication and support. The goal of the study is to see whether this tool can help older adults feel more confident, informed, and prepared to manage their medications safely while living at home.

Detailed description

The main goal of this study is to find out whether an online self-monitoring tool can help older adults who live alone and have memory concerns or mild changes in thinking manage their medications more safely and easily.

The study will look at whether the tool helps people: (1) take their medications as prescribed; (2) keep track of medication-related problems or concerns; (3) feel more confident managing medications at home; and (4) reduce stress, confusion, or burden that can come with taking multiple medications.

Other Study Goal:

The study will also explore whether older adults are willing and able to use the online tool regularly to track medication safety concerns in their daily lives. This includes looking at how comfortable participants feel using the tool and whether they find it helpful for monitoring their medications, symptoms, and concerns.

What Will Happen in the Study:

Participants will be randomly assigned - like flipping a coin - to one of two groups:

Group 1: Online Tool Group:

Participants in this group will receive training on how to use the online self-monitoring tool. They will use the tool for 3 months to track medication-related problems, symptoms, side effects, or other concerns while at home.

During this time, participants will also (1) receive monthly check-ins about their experience using the tool; (2) get educational information and suggestions based on what they report; (3) receive summaries of their medication self-monitoring journey; and (4) be able to interact with an online chatbot about their medication-related concerns.

Group 2: Usual Care Group:

Participants in this group will continue following their regular medical care and medication instructions for the first 3 months.

During this time, they will complete monthly follow-up assessments with the study team. After the first 3 months, they will have the opportunity to use the online self-monitoring tool for 1 month.

Overall Purpose:

By comparing these two groups, researchers hope to learn whether the online tool is useful, easy to use, and helpful for supporting safer medication management among older adults living alone with memory concerns or mild thinking changes.

Interventions

  • Behavioral HOME-MIND
    HOME-MIND aims to improve medication self-management and reduce perceived medication burden in older adults living alone with subjective or mild cognitive decline. This 3-month intervention includes daily technology-enabled self-monitoring of medication safety events or experiences, personalized educational support informed by self-monitoring data, visualizations and summaries of self-monitoring data on a personal dashboard, and sharing self-monitoring summaries with health care providers to fac

Primary outcome measures

  • Medication self-management [Time frame: From enrollment to the end of the study at 3 months, including monthly assessments.]
Secondary outcome measures (1)
  • Medication burden [Time frame: From enrollment to the end of the study at 3 months, it was assessed at baseline and at 3 months.]

Eligibility criteria

Inclusion criteria

  • Older adults (≥ 65 years old)
  • Living alone (in a non-institutional setting without others)
  • With subjective or mild cognitive decline (a screening test to confirm)
  • Taking at least five prescribed medications concurrently
  • With suboptimal self-reported medication adherence (a screening test to confirm)
  • Having access to a computer or mobile device and internet service
  • Able to read and speak English

Exclusion criteria

  • Having severe cognitive, vision, hearing, or other impairment
  • Unable to use computers or mobile devices
  • Relying on someone else to manage medications

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07659548 · HUM00289265 · 1P30AG086561

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗