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OpenTrials
Completed

NCT Number: NCT02656680

Facebook and Friends: Developing an Effective Online Social Network for Weight Loss

In a pilot randomized trial of 160 obese participants, investigators will test the feasibility of a behavioral weight loss program delivered entirely via Facebook. We will recruit in 2 separate waves of 80 participants each. Participants will be randomized to: 1) a condition with study participants only or 2) to a condition they will be able to invite their friends into (wave 1) or one in which the study team keeps recruitment open to allow enrollment through week 8 (wave 2). All participants will receive behavioral counseling via the private Facebook group from the coaches who are present on the network daily. Participants will track their diet and exercise via a free commercial mobile 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 overarching goal of the research plan is to test ways to leverage mobile technologies and social media to increase the impact, scalability, cost-effectiveness, and dissemination potential of lifestyle interventions that reduce cardiovascular disease (CVD) risk. Mobile technology and social media have the potential to reduce the intensity of traditional prevention interventions and enhance outcome by delivering behavioral strategies in-the-moment and by connecting patients other patients to generate better communication and a social support system for lifestyle changes.

This study includes a behavioral weight loss program delivered entirely via on online social network. The weight loss intervention is based on the Diabetes Prevention Program (DPP), an evidence-based weight loss program focused on lifestyle changes. The goals for the intervention are 175 minutes of moderate physical activity per week and an overall weight loss of 7%. Each participant will get an individualized calorie goal that would facilitate a 1-2 lbs. weight loss weekly. Participants will be connected to one another via Facebook and receive behavioral counseling via posts from coaches who are present on the network daily. Participants will track their diet and exercise via a free commercial mobile app. Participants will be assigned to either a Facebook group allowing the invite of friends (wave 1), a Facebook group with open enrollment through week 8 (wave 2) or a Facebook group including only study participants. If they are assigned to the group including their friends, they have the opportunity to invite their friends to participate in the weight loss group if they are interested in losing weight as well. They will not have a limit as to how many friends they can invite. The friends that are invited will not undergo the same procedures as the Facebook (FB)+friends study participants, but we will provide them with a factsheet and collect minimal information from them. If they are assigned to the group with open enrollment through week 8, additional people will be recruited into that group. Those participants being enrolled between week 1-8 will undergo the same procedures as others besides randomization. The goal of both of these studies is to explore how to build the size of online weight loss groups in such a way that increases participant engagement. Feasibility outcomes include engagement (frequency of posts, likes, and comments and number of completed days of tracking posted) retention, acceptability, and weight loss. Post intervention focus groups will gather feedback on the program.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Participants must be:

  • 18-65 years of age;
  • Have a BMI 27-45 kg/m²;
  • Lives in the United States; and
  • Have daily internet access;

Exclusion criteria

  • Does not post on Facebook at least once per week
  • Comments on someone else's post on Facebook less than once per week
  • Does not currently use a smartphone;
  • Is not familiar with using phone apps;
  • Pregnant and/or lactating;
  • Meets criteria for severe depression on the Patient Health Questionnaire (PHQ-9) (score of >20);
  • Had bariatric surgery, plans to during the study;
  • Has had a weight loss of 5% or greater within previous 3 months;
  • Meets criteria for Binge Eating Disorder;
  • Condition that precludes lifestyle changes (i.e. a condition that prevents physical activity increase or dietary changes);
  • Medications affecting weight;
  • Incapable of walking ¼ mile without stopping;
  • Type 1 or 2 diabetes;
  • Participated in previous weight loss studies under the PI;
  • Has concerns about being in a Facebook group with other faculty, staff, or students from the University of Connecticut;
  • Has concerns about being audiotaped;
  • Inability to provide consent;
  • Prisoners; and
  • Non-English speaking

Treatment and study plan

Continuous Enrollment

Behavioral

Participants will receive a weight loss intervention delivered in an online context. The online coaches will post daily content, respond to questions, address concerns, and encourage engagement. The weight loss intervention is based on the Diabetes Prevention Program (DPP), an evidence-based weight loss program focused on lifestyle changes. The goals for the intervention are 175 minutes of moderate physical activity per week and an overall weight loss of 7%. Each participant will get an individualized calorie goal that would facilitate a 1-2 lbs. weight loss weekly. Participants will also be encouraged to use an app such as MyFitnessPal to track daily diet. For this arm, the study team will keep recruitment open for this condition to allow enrollment of new participants through week 8.

Other names: Open Group

Closed Enrollment

Behavioral

Participants will receive a weight loss intervention delivered in an online context. The online coaches will post daily content, respond to questions, address concerns, and encourage engagement. The weight loss intervention is based on the Diabetes Prevention Program (DPP), an evidence-based weight loss program focused on lifestyle changes. The goals for the intervention are 175 minutes of moderate physical activity per week and an overall weight loss of 7%. Each participant will get an individualized calorie goal that would facilitate a 1-2 lbs. weight loss weekly. Participants will also be encouraged to use an app such as MyFitnessPal to track daily diet.

Other names: Closed Group

Primary outcomes

  1. Engagement

    Time frame: 4 months

    Number of Facebook "likes" and other reactions, replies, posts, and polls per participant during the 16 week program.

  2. Retention

    Time frame: 4 months

    The number of participants who complete the follow-up assessment in each condition.

  3. Number of Participants Rating the Intervention 'Acceptable

    Time frame: 4 months

    Participants will rate acceptability of the online intervention. Acceptability was assessed with a single item during the follow-up survey: "How likely are you to recommend the program to a friend?" (responses on a 5-point Likert scale from not at all likely to very likely). Acceptability was categorized into acceptable, defined as responses of a little bit likely, somewhat likely, likely, and very likely, and unacceptable was defined as response of not at all likely.

Secondary outcomes

  1. Percent Weight Loss

    Time frame: Baseline to 4 months

    We calculated percent weight loss from baseline to 4 months.

  2. Diet

    Time frame: 4 Months

    The percentage of intervention days that a participant tracked diet and/or exercise in MyFitnessPal app. Any entry was counted as a day of tracking.

Sponsors and collaborators

Lead sponsor

University of Connecticut

Other

Collaborators

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

Registry information

Official study title

Developing an Effective Online Social Network for Weight Loss

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Jan 15, 2016
Registry last updated
Mar 21, 2024

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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