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NCT05261906Active, not recruiting

The FreeStyle Libre Enabled Reduction of A1c Through Effective Eating and Exercise Study

The Libre Enabled Reduction of A1c Through Effective Eating and Exercise Study: LIBERATE

Source: ClinicalTrials.gov · Last updated 5 Jun 2025

Brief summary (registry, in English)

This two-year multisite, real-world, before-after prospective six-month pilot study utilizing a single-group cohort design (n=184) which will first occur in London, Ontario (n=92) through the St. Joseph's Primary Care for Diabetes Support (PCDSP) program. To test fidelity, the intervention will be delivered again in Hamilton, Ontario through the Hamilton Health Sciences' Boris Clinic in Diabetes Care and Research Program (n=92). Participants will begin by attending the first class at the PCDSP clinic to complete baseline fitness testing as well as receive/set up their wearable technology (FitBit Inspire 2™ and FreeStyle® Libre sensors). Two weeks of baseline data collection will following (glucose values and step counts). Five bi-weekly, followed by three monthly, one-hour videoconferencing group education classes via Microsoft Teams video platform will be offered. Participants will be given the choice to communicate with the LIBERATE clinical team (exercise specialist, physician, and/or registered) weekly between the group classes using their preferred method of communication i.e., email. Classes will offer FreeStyle® Libre-assisted behavioural coaching (i.e., nutrition and exercise). FreeStyle® Libres will be used during the first three months of the program and optionally in the last three months of the intervention. The FitBit Inspire 2™ monitors will be worn for six months. Participants are provided the option to receive individualized aerobic and resistance training prescriptions. The primary outcome is change in glycated hemoglobin. A main goal of this study is to create a "toolkit" for other Canadian Diabetes Management centres (DMCs) to use in the future.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
184 (estimated)
First submitted
27 Jan 2022
Start date
26 Sept 2022
Primary completion date
Oct 2025
Lead sponsor
Western University, Canada
NCT number
NCT05261906

What you commit to

  • Study type: Interventional
  • Planned participants: 184
  • From 26 Sept 2022 to the primary completion date, Oct 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • • Lack of access/knowledge of technology that would prevent virtual participation (Self-reported)
    • • Language barrier, severe mental illness, cognitive impairment or significant/unstable psychiatric disease limiting group participation
    • Pregnancy
    • Active or untreated conditions that would preclude the safe participation of exercise i.e., foot ulcer, CVD, uncontrolled HTN, retinopathy, etc.
    • Recent (\<3 months) medically unstable condition i.e., recent MI, stroke, hospitalization, etc.
    • Inability to participate in the full program (e.g., upcoming surgery, relocating, etc.…)

Who the study is looking for

  • \- • Diagnosis of Type 2 diabetes, age \>18 years old
  • Baseline HbA1c ≥ 8.0% (if no recent A1c (last 3 months) you can ask, or we will ask them to complete a new test).
  • Naïve to Flash glucose monitors BUT interested in using this technology
  • Ownership of either a smartphone (iPhone v7 (iOS of 13.2+) or Samsung Galaxy Note 8, S7 Edge, S8, S8+, S9, S10; Google Pixel, Pixel 2, Pixel 2 XL, Pixel 3, Pixel 3 XL, Pixel 4, Pixel 4 X; LG Nexus 5X (with Android OS of 8 or higher). Other smartphones may be compatible but must be confirmed. https://freestyleserver.com/Payloads/IFU/2022/q2/ART39109-002\_rev-J-web.pdf
  • Have an email address
  • Access to Internet connection
  • Physician cleared to participate in exercise

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
St. Joseph's Family Medical and Dental Centre
Coordinator of this site? Confirm its status
LondonCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.