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University Of Pennsylvania Weight Loss Study

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University of Pennsylvania

Status

Completed

Conditions

Weight Loss

Treatments

Behavioral: Deposit Contract with no match
Behavioral: Deposit contract with a 2:1 match
Behavioral: Deposit contract with a 1:1 match

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

This is a 4-arm, randomized controlled trial to evaluate the effectiveness of financial incentives to motivate and sustain long-term weight loss. The study will recruit eligible employees at a large health management company to participate in a 6-month weight loss program and have weight measurements for an additional 3-month follow-up period. The primary outcome measure in this randomized controlled trial will be pounds of weight lost. The experimental groups will include variations of deposit contracts (participants put their own money at risk, and lose that money if they fail to achieve their weight loss goal) and fixed payments. The use of deposit contracts is a powerful mechanism for inducing behavior change that is based on loss aversion, a psychological concept first described by Nobel Prize winner Daniel Kahneman and Amos Tversky in 1979. A deposit contract takes advantage of the fact that people typically feel the pain of a loss more than the pleasure of a gain, increasing ones motivation to reach a goal.

The study hypotheses are 1) mean weight loss will be greater in all intervention groups compared to the control group by the end of 24 weeks; and 2) individuals in the intervention groups will have a lower mean weight at the end of the 3-month follow-up period than individuals in the control group.

Enrollment

132 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 18 to 70 (inclusive)
  • BMI between 30 and 50 (inclusive)

Exclusion criteria

  • Inability to consent
  • No known Illiteracy and/or inability to speak, read, and write English
  • Participation in another weight loss program
  • Participation in another research study
  • Current treatment for drug or alcohol use
  • Consumption of 5 alcoholic drinks per day
  • Myocardial infarction or stroke within the past 6 months
  • Uncontrolled hypertension (defined as BP170 mm Hg systolic or BP110 mm Hg diastolic)
  • Current addiction to prescription medicines or street drugs
  • Serious psychiatric diagnoses (severe depression, schizophrenia)
  • Pregnancy
  • Diabetic and using any medicine besides metformin to control blood sugars
  • Metastatic cancer
  • Unstable medical conditions that would likely prevent the subject from completing the study
  • Previous diagnosis of an eating disorder
  • History of unsafe weight loss behaviors such as binging or the use of laxatives

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

132 participants in 4 patient groups

1
No Intervention group
2
Experimental group
Description:
Deposit contract with a 1:1 match
Treatment:
Behavioral: Deposit contract with a 1:1 match
3
Experimental group
Description:
Deposit contract with a 2:1 match
Treatment:
Behavioral: Deposit contract with a 2:1 match
Experimental 4
Experimental group
Description:
Deposit contract with no match
Treatment:
Behavioral: Deposit Contract with no match

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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