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Recruiting NCT07524205

Glucose and Activity Tracking for Sedentary Behavior Interventions in Older People With Type 2 Diabetes (TRACK T2D)

No phase Interventional Diabetes Mellitus, Type 2

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: SB Intervention.
Who it may be relevant to
Registry conditions: Diabetes Mellitus, Type 2. Basic parameters: from 55 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
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The overarching goal of this explanatory mixed methods study is to evaluate how older people living with type 2 diabetes (T2D) integrate continuous glucose monitor (CGM) and activity data in diabetes self-management, and how this technology supports reduced sedentary behavior (SB) and improved glucose control.

Interventions

  • Behavioral SB Intervention
    Self-monitoring and reminders about sedentary behavior

Primary outcome measures

  • Responsiveness to Fitbit 'stand' prompts [Time frame: Day 10]
Secondary outcome measures (4)
  • Visit Completion Rate [Time frame: Day 10]
  • Wear Time: activePAL [Time frame: Day 10]
  • Wear Time: CGM [Time frame: Day 10]
  • Wear Time: FitBit [Time frame: Day 10]

Eligibility criteria

Inclusion criteria

  • Aged 55 years and older
  • Self-reported T2D for ≥5 years
  • Speak and read English

Exclusion criteria

  • Type 1 diabetes
  • Use of a CGM for ≥1 month in past 1 year
  • Not willing to use/wear the CGM, activPAL, or Fitbit
  • Dementia
  • Any of the following conditions that may impact SB:
  • Severe pulmonary disease
  • Severe osteoarthritis
  • Class III/IV heart failure
  • Require wheelchair or walker

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

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Single group
Masking
Open label
Primary purpose
Supportive care

Study locations

United States · 1 center
  • University of Minnesota — Minneapolis

Identifiers

NCT: NCT07524205 · STUDY00027259

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗