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Building Habits Together Online Weight Loss Program

University of Connecticut logo

University of Connecticut

Status

Completed

Conditions

Obesity

Treatments

Behavioral: Building Habits Together
Behavioral: Getting Healthy Together

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06154213
R34HL145439 (U.S. NIH Grant/Contract)
HR22-0155

Details and patient eligibility

About

The purpose of this pilot trial is to evaluate the feasibility of a lifestyle intervention where participants will all receive online weight loss counseling delivered via a private Facebook group, but be randomized to the Habit app (developed by the investigators) or MyFitnessPal, a commercial calorie tracking app.

Full description

The purpose of this pilot trial is to evaluate the feasibility of a program where 70 adults with overweight or obesity will receive online weight loss counseling delivered via a private Facebook group, but be randomized to the Habit app (developed by the investigators) or MyFitnessPal, a commercial calorie tracking app. Participants randomized to the Habit app will be asked to record their weight daily, monitor their dietary temptations, plan their exercise, and solve diet and exercise related problems. The temptation tracker helps users identify triggers and track when and why those triggers lead to dietary lapses. The exercise planner allows users to plan their exercise for the week and track whether they completed or missed the exercise and why they missed it. The Habit app provides insights to users about the patterns of their dietary lapses and exercise habits. The problem solver feature helps users identify their biggest problem with diet/exercise and then asks a series of questions to help the app provide tailored solutions to the participant to work on. Participants randomized to MyFitnessPal will track their calorie intake and exercise daily during the intervention.

Enrollment

70 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-65 years old
  • Body mass index (BMI) 27-45 kg/m2
  • Wi-Fi connectivity at home
  • Logs into Facebook at least 5 days per week over the past 2 weeks
  • Has posted/replied on Facebook at least once a week in the past 2 weeks
  • Able to participate in the study in English
  • Interested in losing weight

Exclusion criteria

  • Under the age of 18 and over the age of 65
  • BMI under 27 or over 45 at screening; then under 27 at the point of the first weight on scale
  • Does not have Wi-Fi connectivity at home
  • Does not have a Facebook account
  • Does not log into Facebook at least 5 days per week over the past 2 weeks
  • Did not post/reply on Facebook once a week over the past 2 weeks
  • Not able to participate in the study in English
  • Does not live in the United States
  • Not interested in losing weight
  • Pregnant/lactating or plans to become pregnant during study period
  • Reports having bipolar disorder, substance abuse, psychosis, an eating disorder, or severe depression
  • Had bariatric surgery or plans to have surgery during the study
  • Currently taking medication affecting weight
  • Has lost ≥5% of weight in past 3 months
  • Is participating or intends to participate in another weight loss program during the study that provides coaching or problem solving
  • Chronic pain that interferes with the ability to exercise
  • Has Type 1 Diabetes
  • Has Type 2 Diabetes
  • Unable to make dietary changes or increase physical activity
  • Unable to walk ¼ mile unaided without stopping
  • Currently smokes or vapes nicotine
  • No phone connectivity at home and work
  • Has a digestive disorder/condition that precludes dietary changes
  • Meets criteria for severe depression on the Patient Health Questionnaire (PHQ)-8 (score of >19)
  • Does not currently own a smartphone
  • Smartphone type and/or version not meeting app requirements
  • Participated in previous weight loss studies under the PI
  • Unable to attend the orientation webinar
  • If University of Connecticut (UConn) employee/student has concerns about being in a Facebook group with other UConn faculty, staff, and students
  • Had major surgery in past 6 months and have not been cleared by their doctor to resume physical activity and diet changes
  • Plans to have major surgery in the next 6-months
  • Has an implanted cardiac defibrillator or pacemaker
  • Did not complete screening and on-board processes of study (screening survey, webinar, e-consent, baseline survey, app set-up, scale set-up, etc.)
  • Not willing to be audiotaped for focus groups
  • Prisoner; or
  • Unable to provide consent

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

Building Habits Together
Experimental group
Description:
The Building Habits Together arm includes the 24-week, Facebook-delivered lifestyle intervention based on the Diabetes Prevention Program and use of the Habit app (temptation tracking, exercise planning, and problem solving features).
Treatment:
Behavioral: Building Habits Together
Getting Healthy Together
Active Comparator group
Description:
The Getting Healthy Together arm includes the 24-week, Facebook-delivered lifestyle intervention based on the Diabetes Prevention Program and use of the MyFitnessPal app (daily calorie tracking, exercise tracking).
Treatment:
Behavioral: Getting Healthy Together

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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