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

Primary Purpose

Weight Loss

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
FB + Friends
FB Only
Sponsored by
University of Connecticut
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Weight Loss

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Participants must be:

  1. 18-65 years of age;
  2. have a BMI 30-45 kg/m²;
  3. have written clearance from their primary care provider to participate; and
  4. have daily internet access;

Exclusion Criteria:

  1. Age under 18 or over 65;
  2. BMI under 25 or over 45;
  3. No medical clearance from primary care provider;
  4. Inactive on Facebook;
  5. Does not currently use a smartphone;
  6. Is not familiar with using phone apps;
  7. Plans to move during study;
  8. Pregnant/lactating;
  9. Had bariatric surgery, plans to during the study, or had recent weight loss;
  10. Condition that precludes lifestyle changes (i.e. a condition that prevents physical activity increase or dietary changes);
  11. Medications affecting weight;
  12. Incapable of walking ¼ mile without stopping;
  13. Type 1 or 2 diabetes;
  14. Participated in previous weight loss studies under the PI;
  15. Is a UMass/UConn employee and is uncomfortable participating in a Facebook group with other UMass/UConn employees
  16. Unable to attend the orientation visit;
  17. Inability to provide consent;
  18. Prisoners; and
  19. Has concerns about being audiotaped

Friends of the subjects participating in the FB+friends and FB w/o friends conditions:

  1. Must be: at least 18 years old;
  2. BMI of 25 or over; and
  3. Have an interest in losing weight.

Sites / Locations

  • University of Connecticut

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

FB+Friends

FB Only

Arm Description

FB+Friends is a Facebook-delivered weight loss intervention. For this group, the study team continued to enroll participants through week 8.

FB Only Facebook-delivered weight loss intervention including only study participants.

Outcomes

Primary Outcome Measures

Engagement
Number of Facebook "likes" and other reactions, replies, posts, and polls per participant during the 16 week program.
Retention
The number of participants who complete the follow-up assessment in each condition.
Number of Participants Rating the Intervention 'Acceptable
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 Outcome Measures

Percent Weight Loss
We calculated percent weight loss from baseline to 4 months.
Diet
The number of intervention days that a participant tracked diet and/or exercise in MyFitnessPal app. Any entry was counted as a day of tracking.

Full Information

First Posted
January 7, 2016
Last Updated
March 19, 2021
Sponsor
University of Connecticut
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT02656680
Brief Title
Facebook and Friends: Developing an Effective Online Social Network for Weight Loss
Official Title
Developing an Effective Online Social Network for Weight Loss
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
February 1, 2018 (Actual)
Primary Completion Date
February 20, 2020 (Actual)
Study Completion Date
March 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Connecticut
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Weight Loss

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
134 (Actual)

8. Arms, Groups, and Interventions

Arm Title
FB+Friends
Arm Type
Experimental
Arm Description
FB+Friends is a Facebook-delivered weight loss intervention. For this group, the study team continued to enroll participants through week 8.
Arm Title
FB Only
Arm Type
Active Comparator
Arm Description
FB Only Facebook-delivered weight loss intervention including only study participants.
Intervention Type
Behavioral
Intervention Name(s)
FB + Friends
Other Intervention Name(s)
Continuous Enrollment
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
FB Only
Other Intervention Name(s)
Closed Enrollment
Intervention Description
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.
Primary Outcome Measure Information:
Title
Engagement
Description
Number of Facebook "likes" and other reactions, replies, posts, and polls per participant during the 16 week program.
Time Frame
4 months
Title
Retention
Description
The number of participants who complete the follow-up assessment in each condition.
Time Frame
4 months
Title
Number of Participants Rating the Intervention 'Acceptable
Description
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.
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Percent Weight Loss
Description
We calculated percent weight loss from baseline to 4 months.
Time Frame
Baseline to 4 months
Title
Diet
Description
The number of intervention days that a participant tracked diet and/or exercise in MyFitnessPal app. Any entry was counted as a day of tracking.
Time Frame
4 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Participants must be: 18-65 years of age; have a BMI 30-45 kg/m²; have written clearance from their primary care provider to participate; and have daily internet access; Exclusion Criteria: Age under 18 or over 65; BMI under 25 or over 45; No medical clearance from primary care provider; Inactive on Facebook; Does not currently use a smartphone; Is not familiar with using phone apps; Plans to move during study; Pregnant/lactating; Had bariatric surgery, plans to during the study, or had recent weight loss; 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; Is a UMass/UConn employee and is uncomfortable participating in a Facebook group with other UMass/UConn employees Unable to attend the orientation visit; Inability to provide consent; Prisoners; and Has concerns about being audiotaped Friends of the subjects participating in the FB+friends and FB w/o friends conditions: Must be: at least 18 years old; BMI of 25 or over; and Have an interest in losing weight.
Facility Information:
Facility Name
University of Connecticut
City
Storrs
State/Province
Connecticut
ZIP/Postal Code
06269
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35900824
Citation
Xu R, Divito J, Bannor R, Schroeder M, Pagoto S. Predicting Participant Engagement in a Social Media-Delivered Lifestyle Intervention Using Microlevel Conversational Data: Secondary Analysis of Data From a Pilot Randomized Controlled Trial. JMIR Form Res. 2022 Jul 28;6(7):e38068. doi: 10.2196/38068.
Results Reference
derived
PubMed Identifier
35522466
Citation
Pagoto SL, Schroeder MW, Xu R, Waring ME, Groshon L, Goetz JM, Idiong C, Troy H, DiVito J, Bannor R. A Facebook-Delivered Weight Loss Intervention Using Open Enrollment: Randomized Pilot Feasibility Trial. JMIR Form Res. 2022 May 6;6(5):e33663. doi: 10.2196/33663.
Results Reference
derived

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

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