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Completed

NCT Number: NCT06154213

Building Habits Together Online Weight Loss Program

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Connecticut

Storrs, Connecticut, 06269, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Building Habits Together

Behavioral

Private, hidden Facebook group "Building Habits Together" includes 24 weeks on content based on the Diabetes Prevention Program and the Habit app.

Getting Healthy Together

Behavioral

Private, hidden Facebook group "Getting Healthy Together" includes 24 weeks on content based on the Diabetes Prevention Program and the MyFitnessPal app.

Primary outcomes

  1. Mobile App Use

    Time frame: 24 weeks

    Investigators will calculate the number of days participants used their assigned app

  2. Retention

    Time frame: 24 weeks

    Investigators will calculate retention as the proportion of participants who provide weight data at the 24 week follow-up

  3. Engagement Per Participant in the Facebook Group

    Time frame: 24 weeks

    For each participant, investigators will calculate total engagement in the Facebook group as defined as reactions (e.g., like, care, wow, etc.), replies, posts, and poll votes during the 24-week program. Then we will calculate mean or median engagement per participant over 24 weeks.

  4. Ease of Use (Acceptability)

    Time frame: 24 weeks

    Participants will rate how easy it was to use their assigned app (% who strongly agree/agree)

  5. Contamination

    Time frame: 24 weeks

    Investigators will report the percent of participants in the Habit condition that used MyFitnessPal or other calorie tracking apps during the program.

  6. Time Consuming (Burden)

    Time frame: 24 weeks

    Participants will rate their assigned app in terms of whether they felt it took too much time out of their day (% who strongly agree/agree)

Secondary outcomes

  1. Percentage of Baseline Weight Lost at 24 Weeks

    Time frame: 24 weeks

    Investigators will calculate percent weight change from baseline at 24 weeks

Sponsors and collaborators

Lead sponsor

University of Connecticut

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)
  • Worcester Polytechnic Institute

Registry information

Official study title

Building Habits Together Online Weight Loss Program: Pilot Trial

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Dec 4, 2023
Registry last updated
Mar 30, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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