Menu
Not yet recruiting NCT07734259

Voice-activated and Touchscreen-controlled Smart Speaker Intervention for Older Adults With Poorly Controlled Type 2 Diabetes

No phase Interventional Diabetes Diabetes (DM) Type 2 Diabetes

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: VATC-SS Intervention.
Who it may be relevant to
Registry conditions: Diabetes, Diabetes (DM), Type 2 Diabetes. Basic parameters: from 50 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 →

Overview

This is a pre-post pilot study that will test the feasibility and acceptability of a health educator delivered diabetes education and skills training intervention using a voice-activated, touch screen controlled, smart speaker. We will enroll 30 adults aged 50 and older with poorly controlled type 2 diabetes as defined by a hemoglobin A1C of 8% in the study.

Interventions

  • Behavioral VATC-SS Intervention
    Individuals in the VATC-SS intervention will receive weekly diabetes education and skills training calls for 12 weeks from a health educator through the voice-activated, touch screen controlled smart speaker.

Primary outcome measures

  • HemoglobinA1C [Time frame: Baseline and 3-months post enrollment]
  • Blood Pressure [Time frame: Baseline and 3-months post-enrollment]
  • Low-Density Lipoprotein Cholesterol [Time frame: Baseline and 3-months post-enrollment]
Secondary outcome measures (3)
  • Depression [Time frame: Baseline and 3-months post-enrollment]
  • Social Isolation [Time frame: Baseline and 3-months post-enrollment]
  • Loneliness [Time frame: Baseline and 3-months post-enrollment]

Eligibility criteria

Inclusion criteria

  • 1\) Aged 50 and older; 2) clinical diagnosis of poorly controlled type 2 diabetes, defined as HbA1C greater than or equal to 8% at the screening visit; 3) willing to install and use the VATC-SS for the 3 months of the study.

Exclusion criteria

  • 1\) Mental confusion at screening assessment suggesting significant dementia; 2) alcohol or drug abuse/dependency at screening assessment; 3) active psychosis or acute mental disorder at screening assessment.

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

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Health services research

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07734259 · PRO00058852

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗