CClinicalTrials.gg
CompletedNCT02731768Updated Sep 18, 2018

Nutrition, Exercise, and Technology for Weight Loss

An interventional study of Standard and Social support-enhanced in Overweight and Obesity, sponsored by University of South Carolina. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-09-18.

Sponsored by University of South Carolina · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to evaluate whether a social support-enhanced, technology-based, behavioral weight control intervention can improve weight loss over existing best practices.

Read the detailed description

This 4-month randomized controlled trial is designed to investigate the short-term efficacy and feasibility of a novel, social support-enhanced behavioral weight control intervention. Participants will be recruited via email listservs, fliers, and word of mouth. They will be randomized to a standard behavioral weight control treatment (SBT) or a social support-enhanced behavioral weight control treatment which receives the same intervention as SBT plus social support resources (specifically, additional self-monitoring technologies) for weight loss.

02

Conditions studied

  • Overweight
  • Obesity
03

In context

Overweight

3,670 studies on the registry are indexed under Overweight; 849 are open to participants now.

This study's enrollment of 36 is below the median of 73 across 3,175 interventional studies indexed under Overweight.

Browse Overweight studies →

Lead sponsor

University of South Carolina is the lead sponsor of 191 studies on the registry; 41 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Body mass index (BMI) between 25 kg/m2 and 55 kg/m2
  • Age 18 years or older
  • Access to a computer with an Internet connection
  • Smartphone ownership (Android or iOS)
  • Willing to be randomized to either one of the two study groups
  • Only one member of the same household eligible to participate

Exclusion criteria

Exclusion Criteria:

  • Currently lactating, pregnant, or planning to become pregnant during the length of the study
  • Been diagnosed with type 1 or type 2 diabetes
  • Medical or physical contraindications or limitations for engaging in physical activity
  • History of major medical or psychiatric conditions
  • Recent changes in medication known to affect weight
  • Schedule that would prohibit or restrict attendance at a designated time for weekly in- person group meetings
  • Currently participating in a weight management program
  • Currently on medication that might affect weight loss
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
36 participants (actual)

Study arms

  • Active comparator
    Standard

    Participants will receive an evidence-based behavioral weight control program focused on physical activity and reducing caloric intake. They will be provided with a Fitbit Zip and digital body weight scale for self-monitoring of physical activity and body weight, respectively. They will track caloric intake via the MyFitnessPal smartphone application. They will have access to a study website and attend weekly, in-person group counseling sessions.

    Behavioral: Standard · Device: Fitbit Zip · Device: Digital body weight scale

  • Experimental
    Social support-enhanced

    Participants will receive the same intervention components as the Standard group, as well as two extra Fitbit Zips and digital body weight scales to share with up to two persons in their social circle who will be invited to serve as their support partners.

    Behavioral: Social support-enhanced · Device: Fitbit Zip · Device: Digital body weight scale

Interventions

  • BehavioralStandard

    Participants will receive an evidence-based behavioral weight control program focused on physical activity and reducing caloric intake. They will be provided with a Fitbit Zip and digital body weight scale for self-monitoring of physical activity and body weight, respectively.They will track caloric intake via the MyFitnessPal smartphone application. They will have access to a study website and attend weekly, in-person group counseling sessions.

  • BehavioralSocial support-enhanced

    Participants will receive the same intervention components as the Standard group.Participants will also be provided with two extra Fitbit Zips and digital body weight scales to share with up to two persons in their social circle who will be invited to serve as their support partners.

  • DeviceFitbit Zip
  • DeviceDigital body weight scale
06

What researchers measure

Primary outcomes

  1. Change from Baseline Body Weight at 4 and 12 months

    Time frame: 0, 4, and 12 months

Secondary outcomes

  1. Change from Baseline in Social Support for Exercise (Social Support for Exercise Scale) at 4 and 12 months

    Item scores will be averaged for each respective scale, yielding a final score for each participant. Change in average scores on each scale for each group will be computed.

    Time frame: 0, 4, and 12 months

  2. Change from 2-month Autonomy Support (Important Other Climate Questionnaire) at 4 and 12 months

    Item scores will be averaged for the questionnaire, yielding a final score for each participant. Change in average scores for each group will be computed.

    Time frame: 2, 4, and 12 months

  3. Change from Baseline Motivation for Weight Control (Treatment Self-regulation Questionnaire) at 4 months

    Item scores will be averaged for the questionnaire on three subscales (autonomous, controlled, and amotivation), yielding a final score for each subscale for each participant. Change in average scores on each subscale for each group will be computed.

    Time frame: 0 and 4 months

  4. Change from Baseline Appropriate and Inappropriate Weight Control Practices (Weight Control Practices Checklist) at 4 and 12 months

    Total number of reported appropriate and inappropriate weight control practices will be computed for each participant. Change in the mean number of reported appropriate and inappropriate weight control practices for each group will be computed.

    Time frame: 0, 4, and 12 months

  5. Change from Baseline Social Support Through Technology (2-item questionnaire - level of support and type of support through technology) at 4 and 12 months

    Change in average score on level of support obtained through technology for each group will be computed. Change in the type of support obtained through technology will be described using frequency counts and percentages for each group.

    Time frame: 0, 4, and 12 months

  6. Change from Baseline Average Daily Step Counts measured via BodyMedia SenseWear armband (one-week time period) at 4 and 12 months

    Time frame: 0, 4, and 12 months

  7. Change from Baseline in Social Support for Eating Habits (Social Support for Eating Habits Scale) at 4 and 12 months

    Time frame: 0, 4, and 12 months

  8. Change from Baseline in Social Support for Weight Loss (Social Support for Weight Loss Scale) at 4 and 12 months

    Time frame: 0, 4, and 12 months

Other outcomes

  1. Participant Satisfaction (Satisfaction Questionnaire)

    Time frame: 4 and 12 months

  2. Participant Engagement-chat sessions

    Number of chat sessions attended - recorded by investigator; number of days self-monitored diet on MyFitnessPal and physical activity on Fitbit - recorded by investigator; number of days self-monitored weight - self-reported via a weekly question on study website; number of log-ins to study website - objectively tracked via computer

    Time frame: 0-4 months (all weeks)

  3. Participant Engagement-diet and physical activity

    Number of days self-monitored diet on MyFitnessPal and physical activity on Fitbit-recorded by investigator

    Time frame: 0-4 months (all weeks)

  4. Participant Engagement-weight

    Number of days self-monitored weight-self-reported via a weekly question on study website

    Time frame: 0-4 months (all weeks)

  5. Participant Engagement-log-ins

    Number of log-ins to study website-objectively tracked via computer

    Time frame: 0-4 months (all weeks)

07

Study locations

1 site
  • University of South Carolina
    Columbia, South Carolina 29208, United States
08

References and documents

Individual participant data

Plan to share: No — Data will only be reported in aggregate.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02731768
Lead sponsor
University of South Carolina
Responsible party
Sponsor
First posted
Apr 8, 2016
Start date
Jan 2016
Primary completion
Feb 2017
Completion
Feb 2017
Last update
Sep 18, 2018

Study contacts

Courtney Monroe, PhD
principal investigator · University of South Carolina

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2018. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion