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NCT05579704Completed

Digital Intervention for Behaviour Change and Chronic Disease Prevention

Source: ClinicalTrials.gov · Last updated 27 Mar 2025

Brief summary (registry, in English)

Body weight, diet quality, physical activity, stress, sleep and alcohol use will be evaluated in a sample of 180 Albertans with excess body weight. Participants will be randomized into the following two groups; active control arm (access to a preventative self-care web-based platform for 16 weeks) vs. intervention arm (access to a preventative self-care web-based platform for 16 weeks plus health professional guidance and supervision).

Status (registry)
Completed
Study type
Interventional
Enrollment
186 (actual)
First submitted
3 Oct 2022
Start date
23 Nov 2022
Primary completion date
1 Nov 2024
Lead sponsor
University of Alberta
Diseases
Obesity
NCT number
NCT05579704

What you commit to

  • Study type: Interventional
  • Participants enrolled: 186
  • From 23 Nov 2022 to the primary completion date, 1 Nov 2024
  • 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.

Prior treatment

  • Taking any medication or supplements that may alter energy metabolism, body weight and composition, as evaluated by study investigators;
  • Previous bariatric surgery
  • Active substance abuse (alcohol, cannabis, illicit drugs, prescription drugs)

Other illness

  • Chronic conditions in which weight loss is not indicated or controversial. Significant medical self-reported comorbidities, including uncontrolled metabolic disorders (e.g., cancer, thyroid, stroke, kidney, liver, respiratory, heart disease, type 1 or uncontrolled type 2 diabetes)
  • Self-reported eating disorders, untreated depression, anxiety or other mood disorders

Other

  • Participating in intensive lifestyle interventions, structured exercise programming (\> 3hrs of vigorous physical activity per week) or structured diet programming
  • Weight loss greater than 25 lbs (11 kg) in the past 6 months
  • Unable to adhere to the study protocol

Who the study is looking for

  • Albertans with excess body weight (BMI 30-35 kg/m2)
  • Individuals who are seeking weight loss as screened by the S-Weight Questionnaire
  • Ages 40-65 years of age, any sex/gender
  • Able to safely exercise as screened by the 2022 Physical Activity Readiness Questionnaire (PAR-Q+)
  • Must have a cell phone with internet access and Bluetooth capabilities
  • Able to participate in video conferencing on evenings and/or weekends
  • Willing to wear a Fitbit activity monitor on the wrist for 16 weeks.
  • Able to speak, read and understand English

Age in the registry: 40 years to 65 years · Sex: All · Accepts 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
University of Alberta
Coordinator of this site? Confirm its status
EdmontonCanadaUnknown status

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