ClinicalTrials.gg
CompletedNCT02853877HELPUpdated Apr 18, 2017

Helping Employees Lose Pounds

An interventional study of Weekly Incentive in Weight Loss, sponsored by University of Michigan. Completed at 1 site in United States. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2017-04-18.

Sponsored by University of Michigan · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
62
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

This study will evaluate the effectiveness of financial incentives and messaging tailored to individual goals and aspirations to promote and sustain weight loss. This is a 2-arm randomized controlled trial that will recruit eligible employees at a large university to participate in a 3-month weight loss program, followed by a 3-month follow-up period. The primary outcome will be change in autonomous motivation for weight loss.

The study hypothesis is that intervention group participants will have a greater increase in autonomous motivation for weight loss than participants in the control group at 12 weeks.

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Conditions studied

  • Weight Loss

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03

In context

Weight Loss

1,820 studies on the registry are indexed under Weight Loss; 286 are open to participants now.

This study's enrollment of 62 is below the median of 73 across 1,540 interventional studies indexed under Weight Loss.

Browse Weight Loss studies →

Lead sponsor

University of Michigan is the lead sponsor of 1,503 studies on the registry; 189 are open to participants now.

Of its 167 completed or terminated interventional studies of FDA-regulated products, 132 (79%) have results posted.

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

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Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Interested in losing weight
  • Body Mass Index between 30 and 40 kg/m2
  • Have wireless internet at home
  • Have Android or iOS smart device
  • Willing to record themselves weighing in on a scale or let a family member record them weighing in on a scale

Exclusion criteria

Exclusion Criteria:

  • Pregnant or lactating, or intending to become pregnant in the next 6 months
  • Taking medication (other than metformin) for diabetes to control blood sugar
  • Having a serious psychiatric diagnosis, unstable medical conditions or experienced a heart attack or stroke in the past 6 months
  • Having a history of drug or alcohol abuse or addiction to prescription medications
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Study design

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

Study arms

  • Experimental
    Weekly Incentive

    Participants in the Weekly Incentive arm will be asked to weigh in each week during a 12 week intervention period. They will receive tailored messages and have an opportunity to win a financial reward each week they meet their weight loss goal. Participants will be asked to complete a final weight measurement at week 24.

    Behavioral: Weekly Incentive

  • No intervention
    Weekly Weigh-In

    Participants in the Weekly Weigh-In arm will be asked to weigh in each week during a 12 week intervention period. Participants will be asked to complete a final weight measurement at week 24.

Interventions

  • BehavioralWeekly Incentive

    The tailored incentives intervention aims to assess the impact of tailored messaging and financial incentives on weight loss among obese employees.

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What researchers measure

Primary outcomes

  1. Change in autonomous motivation as measured by the Treatment Self-Regulation Questionnaire

    Time frame: 12 weeks

Secondary outcomes

  1. Change in weight as measured by participant weight measurements using Withings scales

    Time frame: 12 weeks and 24 weeks

Other outcomes

  1. Change in autonomous motivation as measured by the Treatment Self-Regulation Questionnaire

    Time frame: 24 weeks

  2. Change in physical activity as measured by the short form of the International Physical Activity Questionnaire

    Time frame: 12 weeks and 24 weeks

  3. Change in eating behaviors as measured by the Three Factor Eating Questionnaire

    Time frame: 12 weeks and 24 weeks

  4. Change in participation in weight-related wellness programs as measured by responses to the question "In the past 3 months, have you participated in any health and wellness programs?"

    Time frame: 12 weeks and 24 weeks

  5. Change in self-efficacy to lose weight as measured by the Perceived Competence Scale

    Time frame: 12 weeks and 24 weeks

  6. Change in stage of change for weight loss as measured by responses to the questions "Are you currently trying to lose weight?" and "Do you intend to try to lose weight in the near future?"

    Time frame: 12 and 24 weeks

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Study locations

1 site
  • University of Michigan
    Ann Arbor, Michigan 48109, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Aug 2016 to primary completion in Jan 2017, 5 months.

Of 682 non-industry interventional studies with no phase under Weight Loss, half reached primary completion within 22 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 43. This study's 5 months is below that.

Counting every sponsor, half of 737 studies reached it within 22 months; a quarter within 9 and three quarters within 41.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 27, 2016
First posted
Aug 3, 2016
StartActual
Aug 2, 2016
Primary completionActual
Jan 4, 2017
CompletionActual
Apr 7, 2017
Last update
Apr 18, 2017
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 18, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02853877
Responsible party
Jeffrey T. Kullgren (Assistant Professor, University of Michigan) — Principal investigator
First posted
Aug 3, 2016
Start date
Aug 2, 2016
Primary completion
Jan 4, 2017
Completion
Apr 7, 2017
Last update
Apr 18, 2017

Study contacts

Jeffrey T Kullgren, MD,MS,MPH
principal investigator · University of Michigan

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2017. You cannot join it, but the record below documents what was studied.

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