Financial Incentive–Based Approaches for Weight Loss A Randomized Trial Context Identifying effective obesity treatment is both a clinical challenge and a pub-
lic health priority due to the health consequences of obesity. Objective To determine whether common decision errors identified by behavioral
economists such as prospect theory, loss aversion, and regret could be used to designan effective weight loss intervention. Design, Setting, and Participants Fifty-seven healthy participants aged 30-70
years with a body mass index of 30-40 were randomized to 3 weight loss plans: monthlyweigh-ins, a lottery incentive program, or a deposit contract that allowed for partici-
pant matching, with a weight loss goal of 1 lb (0.45 kg) a week for 16 weeks. Par-
ticipants were recruited May-August 2007 at the Philadelphia VA Medical Center in
Pennsylvania and were followed up through June 2008. Main Outcome Measures Weight loss after 16 weeks. Results The incentive groups lost significantly more weight than the control group (mean, 3.9 lb). Compared with the control group, the lottery group lost a mean of
13.1 lb (95% confidence interval [CI] of the difference in means, 1.95-16.40; P=.02)
and the deposit contract group lost a mean of 14.0 lb (95% CI of the difference in
means, 3.69-16.43; P =.006). About half of those in both incentive groups met the
16-lb target weight loss: 47.4% (95% CI, 24.5%-71.1%) in the deposit contract group
to help reduce the rate of obesity in the
and 52.6% (95% CI, 28.9%-75.6%) in the lottery group, whereas 10.5% (95% CI,
1.3%- 33.1%; P=.01) in the control group met the 16-lb target. Although the net
weight loss between enrollment in the study and at the end of 7 months was larger in
the incentive groups (9.2 lb; t=1.21; 95% CI, −3.20 to 12.66; P=.23, in the lotterygroup and 6.2 lb; t=0.52; 95% CI, −5.17 to 8.75; P=.61 in the deposit contract group)
than in the control group (4.4 lb), these differences were not statistically significant.
However, incentive participants weighed significantly less at 7 months than at the study
start (P=.01 for the lottery group; P=.03 for the deposit contract group) whereas con-
Conclusions The use of economic incentives produced significant weight loss dur-
ing the 16 weeks of intervention that was not fully sustained. The longer-term use of
Trial Registration clinicaltrials.gov Identifier: NCT00520611
efits, such as enjoying good health.4,5Drawing on prior work suggesting thatthe same decision errors that hurt
Author Affiliations are listed at the end of this article. Corresponding Author: Kevin G. Volpp, MD, PhD, Center for Health Incentives, Leonard Davis Institute
of Health Economics, University of Pennsylvania School
of Medicine and the Wharton School, VA Center for
Health Equity Research and Promotion, 1232 Block-ley Hall, 423 Guardian Dr, Philadelphia, PA 19104-
2008 American Medical Association. All rights reserved.
(Reprinted) JAMA, December 10, 2008—Vol 300, No. 22 2631 Randomization Procedures Figure 1. Flow of Study Participants
Participants were randomized evenly tothe 3 groups using a block size of 6, with
958 Potentially eligible individuals were
stratification based on sex and age(30-49 years vs 50-70 years). Sealed en-
velopes generated by the statisticianwere used within each of the strata so
that the research coordinator who en-rolled the participants did not know the
randomization assignment of the nextparticipant until it had been assigned.
dinator could be blinded to the ran-domization assignment given the na-
Study Protocol
delphia Veterans Affairs Medical Cen-ter and the University of Pennsylvania.
participants were randomly assignedto participate in either a weight-
monitoring program involving monthlyweigh-ins, or the same program with1 of 2 financial incentive plans (de-
posit contract or lottery). At initial en-
covering diet and exercise strategies for
a free scale with precision to 0.2 lb (to
convert to kilograms, multiply by 0.45).
given a chart at the initial visit depict-
ticipation either infeasible (inability to
Study Population
consent, illiteracy, participation in an-
is shown in FIGURE 1. Participants
ments were recruited using mailings.
if they met or exceeded their weight loss
goal. As an incentive for participants to
race or ethnicity selecting from a list on
2632 JAMA, December 10, 2008—Vol 300, No. 22 (Reprinted)
2008 American Medical Association. All rights reserved.
goal at the end of the month weigh-in.
the end of each month to be weighed.
tract group could earn as little as $0 or
10/19 in the lottery group), of those, 18
but only if, prior to the lottery being re-
or below their weight loss goal. The lot-
who lost at least 20 lb). In addition, all
Statistical Analyses
ated every day. If the first digit gener-
ated was a “2” or the last digit was a“7”
intervals for those failing to attain goals.
tent-to-treat analyses, adjusted for base-
ber was “27” (a 1 in 100 chance), the
deposit contract group, those in the lot-
using F tests. All participants lost to fol-
rate and still attain the final 16-lb weight
higher than their weight loss goal at the
start” in which the overall weight loss
“binge diet” to resume receiving incen-
nating, record their weights, and call in
their weight to the project staff by noon.
ticipant lost 2 lb instead of 4 lb in first
2008 American Medical Association. All rights reserved.
(Reprinted) JAMA, December 10, 2008—Vol 300, No. 22 2633
tions using 2-sided t tests to compare
for the stratification variables (sex and
in the baseline characteristics of any of
by Pearson 2 test for categorical vari-
the groups (TABLE 1). The sample was
ables and the t test or Wilcoxon rank
ticipants, a greater proportion of the in-
Table 1. Characteristics of the Study Samplea No. / Total (%) Entire Sample Contract Participant Characteristics
Median total annual household income from all sources
Self-rated importance of controlling weight measured on a
Confidence in ability to lose weight measured on a 0-10 scale,
Abbreviations: BMI, body mass index, calculated as weight in kilograms divided by height in meters squared; GED, general education development. Conversion factor: To convert from pounds to kilograms, multiply by 0.45; from feet to meters, multiply by 0.3; and inches to centimeters, multiply by 2.54.
a No significant differences were found between groups in any of these conditions. 2634 JAMA, December 10, 2008—Vol 300, No. 22 (Reprinted)
2008 American Medical Association. All rights reserved. Table 2. 16-Week Weight Loss Measures by Group
(F1,35 = 6.20; P = .02; 95% CI of the
Contract
1 , 3 5 = 8.55; P = .006; 95% CI of
(TABLE 2). Although only 10.5% (95%
Abbreviation: CI, confidence interval. Conversion factor: To convert pounds to kilograms, multiply by 0.45.
a Difference between incentive and control conditions significant at PՅ.05.
contract group (22=8.59, P=.01). Theodds of achieving the 16-lb weight lossgoal were significantly greater in both
Figure 2. Weight Loss From Enrollment Through Intervention and 7-Month
the daily call-in rate was extremely high
vealed qualitatively similar patterns re-
gardless of age, income, or initial BMI.
tery group (F2.43; P=.13, 95% CI of the
for blacks; t = 3.57; P = .001; 95% CI of
justing for race did not affect the rela-
Participants in each group regained weight following
of 7 months (FIGURE 2). Although the
the conclusion of the intervention. At 4 months, those
in the incentive groups lost significantly more weightthan those in the control group (P=.02 in the lottery
group and P=.006 in the deposit contract group), but
at the 7-month follow-up after enrollment, the weightdifference between groups was no longer statisti-
for the lottery group; 6.2 lb for the de-
cally significant (P=.23 for the lottery group and P=.61
in the deposit contract group). Nevertheless, those in
the incentive groups experienced a net loss betweenenrollment and at the 7-month interval, whereas those
were not statistically significant (t=1.21;
in the control group did not. Error bars indicate 95%
2 = 5.58, P = .06). These participants
P = .23; 95% CI, −3.20 to 12.66 lb for
the lottery group; t = 0.52; P = .61; 95%
CI, −5.17 to 8.75 lb for the deposit con-
(t18= −1.97; P = .06, 95% CI, −9.19 to
posit contract participants was less than
at baseline to only a marginally signifi-
study (t18 = −2.87, P = .01; 95% CI,
cant degree (P = .10); otherwise, fol-
−15.89 to −2.47 for the lottery group;
t18= −2.41; P = .03; 95% CI, −11.67 to
2008 American Medical Association. All rights reserved.
(Reprinted) JAMA, December 10, 2008—Vol 300, No. 22 2635
change that is based on loss aversion, a
weight loss. Lost to follow-up rates were
concept of decision isolation; people re-
effects identified in the behavioral eco-
is the relative cost-effectiveness of dif-
end of the weight loss phase and the fol-
are particularly emotionally attracted to
weight loss in studies of 6 to 12 month’s
loss lost 4.7 pounds and participants of-
frey and colleagues12,13 had earlier dem-
be useful. The persistence of weight loss
feedback was an intrinsic part of the in-
2636 JAMA, December 10, 2008—Vol 300, No. 22 (Reprinted)
2008 American Medical Association. All rights reserved. Role of the Sponsor: Neither the sponsors nor the fun-
challenge of reducing cocaine abuse. In: Chaloupka
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Additional Contributions: We thank Daniel McDonald, 17. Giuffrida A, Torgenson DJ. Should we pay the
MS, Carnegie Mellon University, Pittsburgh, Pennsyl-
patient? review of financial incentives to enhance
significant weight loss. Study staff could
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2008 American Medical Association. All rights reserved.
(Reprinted) JAMA, December 10, 2008—Vol 300, No. 22 2637
BRIEF SUMMARY; CONSULT THE PACKAGE INSERT FOR FULL PRESCRIBING INDICATIONS AND USAGE: Potassium citrate is indicated for the management of renal tubular acidosis (RTA) with calcium stones, hypocitraturic calcium oxalate nephrolithiasis of any etiology, and uric acid lithiasis with or without calcium stones. CONTRAINDICATIONS: UROCIT®-K is contraindicated in patients with hyperkalem
Formulary Drugs Requiring Prior Authorization (PA) for Medical Necessity PLEASE NOTE: HOME SELF-ADMINISTERED INJECTABLES (HSIs) REQUIRE PRIOR AUTHORIZATION **Drugs listed in bold with dual asterisks will have prior authorization requirements lifted for the first 90 days of eligibility when requested in advance by the group. Diagnosis Exceed Before Prior Author