ArticlePDF Available

Voucher-Based Incentives for Naltrexone Treatment Attendance in Schizophrenia and Alcohol Use Disorders

Authors:

Abstract

This study assessed the feasibility of voucher-based incentives for attendance for directly observed naltrexone treatment in a controlled trial for alcohol use disorders in schizophrenia. Cash-value voucher-based incentives were contingent on attendance at three research visits per week over 12 weeks for 61 participants. Vouchers increased in value based on consecutive attendance. Missed visits resulted in reduction of voucher value. Participants attended 82% of all research visits. Average value of vouchers earned was $330 (78% of the maximum possible). Psychotic symptom severity at baseline did not affect the utilization of vouchers, and 94% of participants perceived the incentive system as helpful. The incentive system was well accepted and used despite psychosis severity, and the attendance rate was high, although causality between incentives and attendance could not be examined. A voucher-based incentive system for attendance can be successfully applied in a clinical trial for alcohol dependence treatment in schizophrenia.
PSYCHIATRIC SERVICES ps.psychiatryonline.org March 2008 Vol. 59 No. 3
331100
Objective: This study assessed the
feasibility of voucher-based in-
centives for attendance for di-
rectly observed naltrexone treat-
ment in a controlled trial for al-
cohol use disorders in schizo-
phrenia. Methods: Cash-value
voucher-based incentives were
contingent on attendance at three
research visits per week over 12
weeks for 61 participants. Vouch-
ers increased in value based on
consecutive attendance. Missed
visits resulted in reduction of
voucher value. Results: Partici-
pants attended 82% of all re-
search visits. Average value of
vouchers earned was $330 (78%
of the maximum possible). Psy-
chotic symptom severity at base-
line did not affect the utilization
of vouchers, and 94% of partici-
pants perceived the incentive sys-
tem as helpful. Conclusions: The
incentive system was well accept-
ed and used despite psychosis
severity, and the attendance rate
was high, although causality be-
tween incentives and attendance
could not be examined. A vouch-
er-based incentive system for at-
tendance can be successfully ap-
plied in a clinical trial for alcohol
dependence treatment in schizo-
phrenia. (Psychiatric Services 59:
310–314, 2008)
Comorbid alcohol use disorders
are known to have significant
adverse effects on the course of
schizophrenia and are associated
with worsening of psychiatric symp-
toms and increased risk of rehospi-
talization (1). Naltrexone is an effec-
tive pharmacotherapy for alcohol
dependence, and several studies
have found that it can reduce alco-
hol use by patients with schizophre-
nia (2,3). Adherence is essential to
naltrexone’s effectiveness; recent
studies have shown significant dif-
ferences in outcomes between nal-
trexone and placebo among only pa-
tients who demonstrated adherence
to more than 80% of possible nal-
trexone doses (4).
Poor adherence to medication is
well documented for patients with
schizophrenia, and among the pa-
tients with this disorder, substance
abuse and dependence are strongly
associated with nonadherence (5).
Patients with serious mental illness
also have poor treatment attendance
and high dropout rates in clinical re-
search trials. Recent meta-analyses
have shown pooled dropout rates
that ranged from 28% to 55% (6). Pa-
tients with schizophrenia also have
poor attendance at outpatient visits,
particularly if they have co-occurring
substance use disorders (7).
Adherence to naltrexone or other
medications could be improved by
ensuring attendance at scheduled
visits. Attendance is particularly cru-
cial for directly observed treatment
interventions, because patients must
be present in order to receive med-
ication. In clinical trials, attendance
is essential for pharmacotherapy, psy-
chotherapy, and administration of re-
search measures. The use of incen-
tives is one possible method to in-
crease attendance and thereby facili-
tate treatment adherence. This ap-
proach has its roots in the token-
economy social learning studies of
the past several decades (8). More
recently, voucher-based incentives
have been shown to be effective in
the treatment of substance use disor-
ders (9). Silverman and colleagues
(10) have shown that abstinence is in-
creased by an incentive system with
escalating rates of reimbursement
based on consecutive drug-free urine
tests.
Only a few studies have extended
the use of incentives in substance
abuse treatment to patients with co-
morbid severe mental illness (3,11–
13). For example, Petrakis and col-
leagues (3) studied a sample of 31 pa-
Voucher-Based Incentives for Naltrexone
Treatment Attendance in Schizophrenia
and Alcohol Use Disorders
LLuubbaa LLeeoonnttiieevvaa,, MM..DD..,, PPhh..DD..
JJaaccqquueelliinnee AA.. DDiimmmmoocckk,, PPhh..DD..
PPaauull WW.. GGaatteellyy,, BB..AA..
LLiissaa GGaalllliinnggeerr
RRoobbeerrtt PPlloouuttzz--SSnnyyddeerr,, PPhh..DD..
SStteevveenn LL.. BBaattkkii,, MM..DD..
Dr. Leontieva, Dr. Dimmock, Mr. Gately,
and Ms. Gallinger are affiliated with the
Department of Psychiatry, State Universi-
ty of New York Upstate Medical Universi-
ty, 750 East Adams St., Syracuse, NY
13210 (e-mail: leontiel@upstate.edu). Dr.
Ploutz-Snyder is also with the university,
at the Center for Outcomes Research and
Evaluation. Dr. Batki is with the Depart-
ment of Psychiatry, University of Califor-
nia, San Francisco, and the San Francisco
Veterans Affairs Medical Center.
BBrriieeff RReeppoorrttss
tients with schizophrenia or schizoaf-
fective disorder and provided incen-
tives in the form of cash reimburse-
ment at a fixed rate of $10 per each
weekly research visit. They achieved
81% retention in a 12-week trial of
naltrexone. Strong Kinnaman and
colleagues (13) used contingent, es-
calating, low-cost, voucher-based in-
centives to reinforce drug-negative
urine tests as a part of the behavioral
treatment of substance use among 59
patients with comorbid serious men-
tal illness, of whom 34% had schizo-
phrenia or schizoaffective disorder.
Although they found that severity of
psychiatric symptoms did not appear
to impair the ability of participants to
utilize incentives, a diagnosis of
schizophrenia was associated with
lower incentive earnings.
To our knowledge, there are no re-
ports of studies using contingent
voucher-based incentives to increase
treatment attendance of patients
with schizophrenia and substance
use disorders. Given that incentive
programs may be useful in research
or clinical treatment settings that re-
quire frequent visits, we report the
application of a voucher-based incen-
tive system for ensuring attendance
by patients with alcohol use disorders
and schizophrenia. We assessed the
effect of psychosis severity and other
variables on utilization of incentives.
Methods
This study analyzed data from the
first 61 participants who entered a
controlled clinical trial funded by the
National Institute on Alcohol Abuse
and Alcoholism, which involved di-
rectly observed treatment with oral
naltrexone or placebo for alcohol use
disorders co-occurring with schizo-
phrenia (14). The target number for
the parent trial is an eventual 90 par-
ticipants; the study is projected to be
completed by June 2008. The goal of
the parent study is to assess the ef-
fectiveness of directly observed nal-
trexone treatment. The incentive sys-
tem was used to recruit and retain
participants. All participants received
incentives for attendance, and there
was no control group because the
parent study was not designed to
evaluate the efficacy of incentives.
This report provides a description
of the voucher-based incentive sys-
tem and its feasibility for use with pa-
tients with schizophrenia or schizoaf-
fective disorder and an alcohol use
disorder. Participants were recruited
from community mental health clin-
ics in Syracuse, New York, and pro-
vided written informed consent ap-
proved by the State University of
New York Upstate Medical Universi-
ty Institutional Review Board. Data
were collected from November 2003
to August 2006. All participants were
confirmed to be in routine outpatient
clinical treatment; all were con-
firmed to be prescribed antipsychot-
ic medications by their clinical treat-
ment providers. The baseline demo-
graphic characteristics of participants
are outlined in Table 1. [A table list-
ing participants’ baseline clinical
characteristics is provided in an on-
line supplement to this brief report at
ps.psychiatryonline.org.] Overall, the
sample was primarily male, single,
Caucasian, and unemployed, and
they earned a low income (most pa-
tients received disability payments).
Participants were asked to attend
three visits per week for directly ob-
served treatment with oral naltrex-
one or placebo over 12 weeks. All re-
ceived weekly motivational counsel-
ing sessions and were seen in re-
search offices located at their respec-
tive outpatient clinical sites. If need-
ed, participants were provided assis-
tance with transportation (with bus
tokens, bus passes, or taxi service).
A monetary-value, voucher-based
incentive system was implemented to
maximize attendance and to reim-
burse participants for their time.
Vouchers were dispensed on comple-
tion of each study visit and could be
exchanged for goods or services at
any time. At each visit, participants
could choose to either use (“spend”)
the vouchers, by asking to exchange
them for items, or save them for fu-
ture use. The voucher-based incen-
tive system was modeled on the work
of Silverman and colleagues (10),
wherein cash-value vouchers in-
PSYCHIATRIC SERVICES ps.psychiatryonline.org March 2008 Vol. 59 No. 3 331111
TTaabbllee 11
Sociodemographic characteristics of 61 study participants with schizophrenia or
schizoaffective disorder and a co-occurring alcohol use disorder
Characteristic N %
Gender
Male 47 77
Female 14 23
Race
Caucasian 27 44
African American 22 36
Other 12 20
Ethnicity
Non-Hispanic 57 93
Hispanic 4 7
Married 5 8
Living independently 41 67
Income source
Disability benefits 44 72
Public assistance or welfare 10 16
Other 4 7
Employment 3 5
Employed 6 10
Payee manages participant’s money 24 39
Age (M±SD) 42±9
Education (M±SD years) 12±2
Monthly income
M±SD $736±$341
Median $666
Interquartile range $587–$912
Money under participant’s control
M±SD $489±$357
Median $482
Interquartile range $180–$690
creased in value with each visit at-
tended and were reset to a lower val-
ue after a missed visit.
In this study, vouchers began at $5
per visit and increased in increments
of $1 for each consecutively attend-
ed visit until a maximum of $10 per
visit was reached. This maximum
level was maintained unless the par-
ticipant missed an appointment. In
the event of an unexcused missed
visit, the voucher value for the next
visit was reset to $5. Participants
could earn a maximum of $425 in
vouchers during the 12-week treat-
ment phase. As in the Silverman
team’s design, this schedule was
meant not only to increase the ab-
solute number of attended visits but
also to reinforce the consistency of
attendance. On the basis of our prior
work (2), a wide range of items—
such as gift certificates to grocery
stores and restaurants, bus tokens,
and portable CD players—were of-
fered in an effort to provide specific
rewards that had high salience to
participants. [An appendix describ-
ing the voucher-based incentive sys-
tem in more detail is provided in an
online supplement to this brief re-
port at ps.psychiatryonline.org.]
The following measures were ad-
ministered at baseline: Positive and
Negative Syndrome Scale (PANSS),
Calgary Depression Scale for Schizo-
phrenia (CDSS), Addiction Severity
Index (ASI), and Time Line Follow
Back (TLFB). At the end of treat-
ment, participants completed an
end-of-study form that included a
question about the helpfulness of the
voucher incentive system (the 5-
point Likert scale of responses
ranged from not helpful at all to very
helpful).
On the basis of their attendance at
the three-times-per-week study vis-
its, participants were classified as ei-
ther consistent attendees, who at-
tended 80% or more of visits, or in-
consistent attendees, who attended
less than 80%. This dichotomy was
based on previous studies of naltrex-
one treatment in which adherence to
naltrexone was defined by whether
80% of doses were taken (4). To cal-
culate attendance percentage, the to-
tal number of completed study visits
was divided by the total number of
possible visits minus the number of
visits missed as a result of circum-
stances beyond the participant’s con-
trol (because of hospitalization, for
example). Voucher spending was as-
sessed by the percentage of visits at
which participants spent some or all
portions of their earned incentives.
Sociodemographic data, psychiatric
status (measured by the PANSS and
CDSS), and alcohol severity (meas-
ured by the ASI and TLFB) were
also measured at baseline.
We used Spearman’s rho correla-
tions to assess the relationships be-
tween spending rates and other con-
tinuous variables (PANNS, CDSS,
and TLFB results). We compared
spending rates by using categorical
variables and Student’s t test or one-
way analysis of variance. We com-
pared continuous outcomes by atten-
dance categories (consistent atten-
dance or inconsistent attendance) us-
ing Student’s t test. Data were ana-
lyzed with SPSS (version 14.1) for
Windows.
Results
Of a possible 38 total research visits
(with visits missed for hospitalization
or incarceration factored out), mean±
SD attendance was 31±10 visits
(82%). Of the 61 participants, 47
(77%) were consistent attendees,
present at 80% or more visits, and 14
(23%) were inconsistent attendees.
Consistent attendees made 96%±5%
of the visits; inconsistent attendees
made 49%±28% of the visits.
The total amount of incentives
earned by 61 participants over the
course of 12 weeks was $20,144. The
amount of incentives earned by each
participant was $330±$123 (78% of
the maximum possible), with a medi-
an of $386 (interquartile range
$274–$425, which was 91% of the
maximum possible). The participants
spent incentives at 42%±22% of their
visits. The descriptions and frequen-
PSYCHIATRIC SERVICES ps.psychiatryonline.org March 2008 Vol. 59 No. 3
331122
TTaabbllee 22
Description, quantity, cost, and frequency of incentives purchased by 61 patients with schizophrenia or schizoaffective
disorder and a co-occurring alcohol use disorder
Purchases Participants who
(N=1,599) Cost made purchases
Category and items N % Total ($)a%N%
Fast-food restaurant gift certificates 718 45 3,845 18 49 80
Groceries (certificates or items) 469 29 3,611 17 34 56
Electronicsb73 5 4,158 20 32 52
Shopping mall or retailer gift certificates 66 4 4,659 22 24 39
Transportation vouchers 162 10 1,492 7 24 39
Clothing 61 4 1,419 7 18 30
Entertainment (CDs, books, and movie
tickets) 19 1 340 2 9 15
Bill payments (for utilities or credit cards) 19 1 1,282 6 8 13
Household items 9 .6 297 1 7 11
Health items 3 .2 149 .7 2 3
aThe grand total of $21,252 is slightly higher than the total amount of incentives earned ($20,144) because some participants saved points earned in
screening visits to purchase items during the study.
bTelevisions, portable players, radios, DVD players or VCRs, and gift certificates to electronics stores
cies of incentives purchased as well
as their quantities and cost are dis-
played in Table 2. The incentives
purchased most frequently were
restaurant gift certificates, followed
by groceries and electronics items.
Spending was inversely correlated
with participants’ income (ρ=–.33,
p<.02) and the amount of funds un-
der participants’ direct control (ρ=
–.36, p<.005). The participants with
a payee who managed their money
were expected to have less direct
control over their funds and were
found to spend significantly more
frequently than participants without
a payee (at 58% of visits versus 28%,
p<.001).
Our t-test comparisons of consis-
tent attendees with inconsistent at-
tendees in regard to demographic
characteristics (age, gender, race,
ethnicity, years of education, marital
and employment status, living situa-
tion, income source, monthly in-
come and amount under control, and
payee status) and clinical character-
istics (measured by the PANSS,
CDSS, ASI, and TLFB) revealed no
significant differences between
groups. Consistent attendees also
were not significantly different from
inconsistent attendees in spending
frequencies.
Utilization of vouchers as meas-
ured by spending rates did not signif-
icantly vary by severity of psychotic
symptoms or depressive symptoms.
Of 53 respondents 94% perceived
the incentive system as very helpful
or helpful (very helpful, 37 partici-
pants, or 70%; helpful, 13 partici-
pants, or 25%). Only three partici-
pants (6%) indicated that their per-
ception of incentives was neutral.
Discussion
Voucher-based incentives that esca-
late in value to ensure attendance at
research visits for directly observed
alcohol pharmacotherapy are feasible
to use and are acceptable for patients
with schizophrenia spectrum disor-
ders. Although Medicaid and other
insurance programs do not cover the
cost of incentives, other potential
funding sources may include com-
munity-based agencies, local busi-
nesses, or government grants.
The incentive system used in this
study was established to maximize at-
tendance and was tailored to individ-
ual study participants. More than
three-quarters of participants were
consistent attendees, attending more
than 80% of visits. This result is par-
ticularly impressive in that the de-
mands placed on participants were
high, with a requirement to attend
three times per week for 12 weeks.
Although these high attendance rates
were attained in the presence of in-
centives, we cannot draw conclusions
regarding causality because there was
no control group and all participants
received incentives. Nearly three-
fourths of participants chose to save
their vouchers rather than immedi-
ately spending them at each visit.
These participants chose to purchase
higher-cost items rather than imme-
diately buying a lower-priced item.
Voucher utilization was not related
to severity of psychotic or other
symptoms, indicating that patients
with schizophrenia spectrum disor-
ders may be cognitively organized
enough to plan ahead and save
vouchers for larger purchases. Par-
ticipants preferred food items over
other incentives, which may be un-
derstandable given that most partici-
pants had low income and nearly
90% were receiving disability in-
come or public assistance. It may be
useful for researchers and clinicians
designing future incentive-based
programs to tailor potential incen-
tives to participants’ sociodemo-
graphic characteristics.
Patterns of spending appeared to
have no significant relationship to de-
mographic characteristics or severity
of psychiatric symptoms, a finding
that supports similar conclusions re-
garding the use of incentives by
Strong Kinnaman and colleagues
(13). Our data provide evidence that
such an incentive system is feasible
and applicable to a diverse popula-
tion with a wide range of demograph-
ic characteristics, psychopathology,
and severity of alcohol use disorder
symptoms.
Economic variables, such as in-
come and the amount of funds under
the participant’s control, affected the
rate of spending versus saving of
vouchers. Participants with more
money available to them under their
direct control may have been able to
better “afford” to save more in com-
parison with those with less money
available for their immediate needs.
Conclusions
It is feasible to apply an escalating
system of voucher-based incentives
to reinforce attendance for directly
observed medication of participants
with schizophrenia and alcohol use
disorders. Participants had high at-
tendance rates, were able to save in-
centives for future larger purchases,
and found the incentives helpful.
The incentive system described here
may be applicable to research and
clinical programs, particularly those
that require frequent attendance for
directly observed treatment or other
intensive interventions. A limitation
of the incentive system reported here
is that it is time-consuming and la-
bor-intensive to implement.
Although broad application of the
incentive system to clinical practice
with patients with co-occurring dis-
orders may be problematic because
of cost, the methodology can be mod-
ified to fit the needs of different clin-
ical settings. Less expensive ap-
proaches have been developed, using
intermittent reinforcement, for ex-
ample, by giving patients a chance to
draw from a jar to win prizes that are
of modest cost (15). Future con-
trolled studies are needed to meas-
ure the efficacy of voucher-based in-
centive systems in improving the
treatment of patients with schizo-
phrenia or schizoaffective disorder
and substance use disorders.
Acknowledgments and disclosures
This work was made possible by grant R01-
AA-013655 from the National Institute on Al-
cohol Abuse and Alcoholism. The authors
greatly appreciate the assistance of Michelle
Cavallerano, B.A., Sara DeRycke, B.S., and
Katherine Strutynski, B.A., in implementing
this research project. The authors also thank
the patients and staff of Hutchings Psychiatric
Center, Syracuse VA Medical Center, and St.
Joseph’s Mental Health for their assistance
with the project.
The authors report no competing interests.
References
1. Westermeyer J: Comorbid schizophrenia
and substance abuse: a review of epidemi-
ology and course. American Journal on Ad-
dictions 15:345–355, 2006
PSYCHIATRIC SERVICES ps.psychiatryonline.org March 2008 Vol. 59 No. 3 331133
PSYCHIATRIC SERVICES ps.psychiatryonline.org March 2008 Vol. 59 No. 3
331144
2. Batki SL, Dimmock JA, Wade M, et al:
Monitored naltrexone without counseling
for alcohol abuse/dependence in schizo-
phrenia-spectrum disorders. American
Journal on Addictions 16:253–259, 2007
3. Petrakis IL, O’Malley S, Rounsaville B, et
al: Naltrexone augmentation of neuroleptic
treatment in alcohol abusing patients with
schizophrenia. Psychopharmacology 172:
291–297, 2004 [Erratum, Psychopharma-
cology (Berlin) 174:300, 2004]
4. Chick J, Anton R, Checinski K, et al: A
multicentre, randomized, double-blind,
placebo-controlled trial of naltrexone in
the treatment of alcohol dependence or
abuse. Alcohol and Alcoholism 35:587–
593, 2000
5. Valenstein M, Blow FC, Copeland LA, et
al: Poor antipsychotic adherence among
patients with schizophrenia: medication
and patient factors. Schizophrenia Bulletin
30:255–264, 2004
6. Kemmler G, Hummer M, Widschwendter
C, et al: Dropout rates in placebo-con-
trolled and active-control clinical trials of
antipsychotic drugs: a meta-analysis.
Archives of General Psychiatry 62:1305–
1312, 2005
7. Coodin S, Staley D, Cortens B, et al: Pa-
tient factors associated with missed ap-
pointments in persons with schizophrenia.
Canadian Journal of Psychiatry 49:145–
148, 2004
8. Dickerson FB, Tenhula WN, Green-Paden
LD: The token economy for schizophrenia:
review of the literature and recommenda-
tions for future research. Schizophrenia
Research 75:405–416, 2005
9. Lussier JP, Heil SH, Mongeon JA, et al: A
meta-analysis of voucher-based reinforce-
ment therapy for substance use disorders.
Addiction 101:192–203, 2006
10. Silverman K, Chutuape MA, Bigelow GE,
et al: Voucher-based reinforcement of co-
caine abstinence in treatment-resistant
methadone patients: effects of reinforce-
ment magnitude. Psychopharmacology
146:128–138, 1999
11. Roll JM, Chermack ST, Chudzynski JE: In-
vestigating the use of contingency manage-
ment in the treatment of cocaine abuse
among individuals with schizophrenia: a
feasibility study. Psychiatry Research
125:61–64, 2004
12. Sigmon SC, Higgins ST: Voucher-based
contingent reinforcement of marijuana ab-
stinence among individuals with serious
mental illness. Journal of Substance Abuse
Treatment 30:291–295, 2006
13. Strong Kinnaman JE, Slade E, Bennett
ME, et al: Examination of contingency
payments to dually-diagnosed patients in a
multi-faceted behavioral treatment. Addic-
tive Behaviors 32:1480–1485, 2007
14. Batki SL, Dimmock JA, Ploutz-Snyder R,
et al: Naltrexone treatment for patients
with schizophrenia and alcohol depend-
ence: the role of adherence—preliminary
findings. Alcoholism Clinical and Experi-
mental Research 31(suppl 6):255A, 2007
15. Pierce JM, Petry NM, Spitzer ML, et al:
Effects of lower cost incentives on stimu-
lant abstinence in methadone maintenance
treatment. Archives of General Psychiatry
63:201–208, 2006
SSuubbmmiissssiioonnss ffoorr DDaattaappooiinnttss CCoolluummnn IInnvviitteedd
Submissions to the journal’s Datapoints column are invited. Datapoints encour-
ages the rapid dissemination of relevant and timely findings related to clinical
and policy issues in psychiatry. National data are preferred. Areas of interest in-
clude diagnosis and practice patterns, treatment modalities, treatment sites, pa-
tient characteristics, and payment sources. The analyses should be straightfor-
ward, so that the figure or figures tell the story. The text should follow the stan-
dard research format to include a brief introduction, description of the methods
and data set, description of the results, and comments on the implications or
meanings of the findings.
Datapoints columns, which have a one-page format, are typically 350 to 400
words of text with one or two figures. The maximum total word count—includ-
ing the title, author names, affiliations, references, and acknowledgments—is
500. Because of space constraints, submissions with multiple authors are dis-
couraged; submissions with more than four authors should include justification
for additional authors.
Inquiries or submissions should be directed to column editors Amy M. Kil-
bourne, Ph.D., M.P.H. (amy.kilbourne@va.gov), or Tami L. Mark, Ph.D. (tami.
mark@thomson.com).
... Naltrexone was associated with reduced drinking by alcohol dependent patients receiving antidepressants for mood and anxiety symptoms [525]. Voucher-based incentives were effective for naltrexone treatment attendance in schizophrenia and alcohol use disorders [565]. Persistence with oral naltrexone was a positive factor for alcohol treatment that might have been due to better prognosis by the patients [522]. ...
Article
This paper is the 31st consecutive installment of the annual review of research concerning the endogenous opioid system. It summarizes papers published during 2008 that studied the behavioral effects of molecular, pharmacological and genetic manipulation of opioid peptides, opioid receptors, opioid agonists and opioid antagonists. The particular topics that continue to be covered include the molecular-biochemical effects and neurochemical localization studies of endogenous opioids and their receptors related to behavior (Section 2), and the roles of these opioid peptides and receptors in pain and analgesia (Section 3); stress and social status (Section 4); tolerance and dependence (Section 5); learning and memory (Section 6); eating and drinking (Section 7); alcohol and drugs of abuse (Section 8); sexual activity and hormones, pregnancy, development and endocrinology (Section 9); mental illness and mood (Section 10); seizures and neurologic disorders (Section 11); electrical-related activity and neurophysiology (Section 12); general activity and locomotion (Section 13); gastrointestinal, renal and hepatic functions (Section 14); cardiovascular responses (Section 15); respiration and thermoregulation (Section 16); and immunological responses (Section 17).
... Based on the results of this study, the most helpful component for participants was the provision of voucher-based incentives for attendance. This finding is consistent with previous literature on the successful use of incentives to reinforce behavior change in patients with schizophrenia (10, 18, 19). The next most helpful aspects of the study for participants were the close monitoring provided by attending research visits three times per week and their report on drinking behavior to research staff. ...
Article
Full-text available
To describe the attitudes of patients and their mental health providers regarding participation in a controlled trial of directly monitored naltrexone (NTX) treatment for alcohol dependence in schizophrenia. Ninety participants with schizophrenia and their providers were asked to report opinions of treatment with oral NTX or placebo 3 times per week for 12 weeks, motivational counseling (MI), and voucher-based incentives (VBI) for attendance. Seventy-nine percent of participants "liked the study a lot," and 94% reported that it was helpful. Study components rated as helpful by participants were: VBI (95% of participants), meeting with staff 3 times per week (84%), reporting alcohol use (82%), MI (82%), reporting psychiatric symptoms (73%), breath alcohol testing (72%), and study medication (57%). Benefits reported by patients were: feeling better mentally (67%), drinking less (52%), feeling better physically (49%), and stopping drinking (27%). Seventy percent of providers reported that the study was helpful. Benefits noted by providers included: reduced drinking (33%), better treatment adherence (32%), stopping drinking (23%), and reduced psychiatric symptoms (22%). Patient/provider responses agreed on helpfulness with stopping or reducing drinking. Most participants with schizophrenia liked participating in a clinical trial of directly observed naltrexone treatment for alcohol dependence, and found incentives for attendance, frequent staff contact and monitoring of drinking, and motivational counseling to be the most helpful. Most participants reported improvement in mental health and reduced drinking. Mental health providers also reported that the study was helpful, but they did not describe the same degree of benefit as did patients.
Thesis
Full-text available
The purpose of this thesis is to examine the impact of financial incentives to promote health behaviour change. Financial incentives include tangible rewards as cash, vouchers and lotteries that are offered to individuals conditional to the fulfilment of health guidelines. Despite the growing use of such patient incentives in practice, some fundamental questions are yet to be answered: (1) Are financial incentives effective? (2) What type and size of incentive is more effective? (3) Do patient income and past health behaviour moderate the impact of incentives? These questions are analysed in the context of (a) blood donation and (b) compliance with health care including adherence to treatment, disease screening, immunisation and appointment keeping. Behavioural economics, in particular prospect theory, provide the theoretical foundations for this work and substantiate my hypotheses about the effect of financial incentives. I perform the first meta-analyses in the literature to quantify the impact of patient financial incentives to promote blood donation (chapter 3) and compliance (chapter 4). These results show that financial incentives do not promote blood donation but increase compliance with health care, particularly for low income patients. Two large field studies were developed to further examine the effect of incentives in compliance - testing pioneer incentive schemes. I test the impact of a certain (£5 voucher) versus uncertain (£200 lottery) incentive framed either as a gain or loss to promote Chlamydia screening (chapter 5). I also develop the first study ever testing preferences for sequences of events in the field – using the naturalistic setting of colorectal cancer. This study compared the effect of a €10 incentive offered at the end of screening versus two €5 incentives offered at the beginning and end of screening (chapter 6). The former showed the voucher framed as a gain was the most effective incentive and the latter showed that smaller two €5 incentives increase screening more than a single €10 incentive (which had a detrimental effect compared to no incentive). I fundamentally contribute to the literature by showing that (i) patient financial incentives do not increase the quantity of blood donations and may have an adverse effect on quality, providing empirical evidence to a long-standing policy debate. Furthermore (ii) small certain rewards around £5 are likely to be the optimal incentive for compliance with health care, (iii) higher incentives may be more effective if offered as smaller segregated incentives of the same amount and (iv) incentives have over twice the impact on low income patients than on more affluent patients.
Article
Full-text available
Many patients with schizophrenia are poorly adherent with antipsychotic medications. The newer, atypical antipsychotics may be more acceptable to patients and result in increased adherence. We used national Department of Veterans Affairs (VA) pharmacy data to examine whether patients receiving atypical agents are more adherent with their medication and explored patient factors associated with adherence. Patients who received a diagnosis of schizophrenia or schizoaffective disorder between October 1, 1998, and September 30, 1999, were identified in the VA National Psychosis Registry. We calculated medication possession ratios (MPRs) for patients filling prescriptions for one (n = 49,003) or two (n = 14,211) antipsychotics during the year. We examined cross-sectional relationships among adherence, type of antipsychotic, and patient characteristics and explored adherence among patients switching antipsychotics during the year. Among patients receiving one antipsychotic, 40 percent had MPRs < 0.8, indicating poor adherence. African-Americans and younger patients were more likely to be poorly adherent. Cross-sectionally, patients on atypical agents were more likely to be poorly adherent (41.5%) than patients on conventional agents (37.8%). However, among a small group of patients switching from a conventional to an atypical agent (n = 1,661) during the year, the percentage who were poorly adherent decreased from 46 percent to 40 percent. We describe the continuum of antipsychotic adherence among a large sample of patients with schizophrenia and confirm that poor adherence is common. African-Americans and younger patients are particularly at risk. Unfortunately, atypical antipsychotics may not be associated with substantial improvements in adherence. More intensive interventions are likely needed.
Article
Full-text available
Dropout rates in randomized clinical trials of antipsychotic drugs have consistently been reported to be high, and the use of a placebo-controlled design is hypothesized to be one of the reasons for this. To investigate this hypothesis in a meta-analysis of available data from pertinent clinical trials. Comprehensive search of PubMed- and MEDLINE-listed journals. Double-blind randomized controlled clinical trials of the second-generation antipsychotics risperidone, olanzapine, quetiapine, amisulpride, ziprasidone, and aripiprazole meeting the following criteria: unselected patient population with a diagnosis of schizophrenia or schizoaffective disorder, change in psychopathologic symptoms as the primary end point, and trial duration of 12 weeks or less. Sample size, mean age, baseline disease severity, dropout rate, trial design, trial duration, and publication year. Thirty-one trials meeting the inclusion criteria were found, comprising 10 058 subjects. Weighted mean dropout rates in the active treatment arms were significantly higher in placebo-controlled trials (PCTs) than in active-control trials: 48.1% (PCTs) vs 28.3% (active-control trials) for second-generation antipsychotics (odds ratio, 2.34; 95% confidence interval, 1.58-3.47) and 55.4% (PCTs) vs 37.2% (active-control trials) for classical antipsychotics (odds ratio, 2.10; 95% confidence interval, 1.29-3.40). Within PCTs, attrition rates were significantly higher in the placebo arms than with second-generation antipsychotics (60.2% vs 48.1%; odds ratio, 1.63; 95% confidence interval, 1.37-1.94). Within the subset of trials in which both second-generation and classical antipsychotics were used, dropout rates were significantly higher with classical antipsychotics. Use of a placebo-controlled design had a major effect on the dropout rates observed. Because high dropout rates affect the generalizability of such studies, it is suggested that, in addition to the PCTs, studies with alternative designs need to be considered when evaluating an antipsychotic's clinical profile.
Article
Voucher-based reinforcement of cocaine abstinence has been one of the most effective means of treating cocaine abuse in methadone patients, but it has not been effective in all patients. This study was designed to determine if we could promote cocaine abstinence in a population of treatment-resistant cocaine abusing methadone patients by increasing the magnitude of voucher-based abstinence reinforcement. Participants were 29 methadone patients who previously failed to achieve sustained cocaine abstinence when exposed to an intervention in which they could earn up to $1155 in vouchers (exchangeable for goods/services) for providing cocaine-free urines. Each patient was exposed in counterbalanced order to three 9-week voucher conditions that varied in magnitude of voucher reinforcement. Patients were exposed to a zero, low and high magnitude condition in which they could earn up to $0, $382, or $3480 in vouchers for providing cocaine-free urines. Analyses for 22 patients exposed to all three conditions showed that increasing voucher magnitude significantly increased patients' longest duration of sustained cocaine abstinence (P<0.001) and percent of cocaine-free urines (P<0.001), and significantly decreased patients' reports of cocaine injections (P=0.024). Almost half (45%) of the patients in the high magnitude condition achieved >/=4 weeks of sustained cocaine abstinence, whereas only one patient in the low and none in the zero magnitude condition achieved more than 2 weeks. Reinforcement magnitude was a critical determinant of the effectiveness of this abstinence reinforcement intervention.
Article
The opioid antagonist, naltrexone, is reported, in single centre studies, to improve the clinical outcome of individuals with alcohol dependence participating in outpatient psychosocial programmes. This is the first multicentre controlled study to evaluate the efficacy and safety of naltrexone as adjunctive treatment for alcohol dependence or abuse. Patients who met criteria for alcohol dependence (n = 169) or alcohol abuse (n = 6) were randomly assigned to receive double-blind oral naltrexone 50 mg daily (n = 90) or placebo (n = 85) for 12 weeks as an adjunct to psychosocial treatment. The primary efficacy variable was time to first episode of heavy drinking; secondary efficacy assessments included time to first drink, alcohol consumption, craving, and changes in the serum biological markers gamma-glutamyl transferase (GGT), and aspartate and alanine aminotransferases. Compliance was assessed by tablet counts and, in the naltrexone-treated group, by measurement of urinary concentrations of 6-ss-naltrexol. Forty-nine (58%) patients randomized to placebo and 53 (59%) randomized to naltrexone did not complete the study. In intention-to-treat analyses, there was no difference between groups on measures of drinking. The median reduction from baseline of serum GGT (P: < 0.05) and the reductions in alcohol craving (Obsessive and Compulsive Drinking Scale: OCDS) were greater in the naltrexone group (P: < 0.05), from approximately half-way through the study. Of 70 patients (35 placebo; 35 naltrexone) who met an a priori definition of compliance (80% tablet consumption, attendance at all follow-up appointments), those allocated to naltrexone reported consuming half the amount of alcohol (P: < 0.05), had greater median reduction in serum GGT activity (P: < 0.05), and greater reduction in alcohol craving (OCDS total score: P: < 0.05; Obsessive subscale score: P: < 0.05), compared to patients in the placebo group. Use of naltrexone raised no safety concerns. Naltrexone is effective in treating alcohol dependence/abuse in conjunction with psychosocial therapy, in patients who comply with treatment.
Article
This small-scale study was conducted to examine the feasibility of using voucher-based reinforcement therapy (VBRT) as a treatment modality for cocaine abuse among individuals with schizophrenia. Cocaine use was reduced in three individuals with a diagnosis of schizophrenia during a VBRT intervention. Interestingly, all of the abstinence occurred during the first half of the intervention. This early period of sobriety may represent a clinically relevant window of opportunity during which intensive psychosocial or social work interventions might have a greater chance for success.
Article
There is limited research on factors that may predict missed appointments. This study examined correlates to missed appointments in a sample of persons attending an outpatient schizophrenia program. We measured the rate of missed appointments for 342 outpatients with severe and persistent mental illness (that is, with diagnoses of schizophrenia, schizoaffective disorder, and delusional disorder) attending a psychiatric outpatient clinic over a period of 2 years and 3 months. We collected and analyzed demographic and clinical variables to ascertain differences between patients with high and low rates of nonattendance. Patients who missed 20% or more of their appointments were significantly younger, were more likely to abuse drugs and alcohol, and manifested lower levels of community functioning. This profile may be useful in helping clinicians to schedule appointments for this clinical population, to identify those who may need community outreach services, and to improve their treatment prospects.
Article
The token economy is a treatment intervention based on principles of operant conditioning and social learning. Developed in the 1950s and 1960s for long-stay hospital patients, the token economy has fallen out of favor since that time. The current review was undertaken as part of the 2003 update of the schizophrenia treatment recommendations of the Patient Outcomes Research Team (PORT). A total of 13 controlled studies of the token economy were reviewed. As a group, the studies provide evidence of the token economy's effectiveness in increasing the adaptive behaviors of patients with schizophrenia. Most of the studies are limited, however, by methodological shortcomings and by the historical context in which they were performed. More research is needed to determine the specific benefits of the token economy when administered in combination with contemporary psychosocial and psychopharmacological treatments.
Article
To systematically investigate the effectiveness of voucher-based reinforcement therapy for the treatment of substance use disorders. Effect sizes and 95% confidence intervals were calculated for studies published between January 1991 and March 2004 that utilized voucher-based reinforcement therapy (VBRT) or related monetary-based incentives to treat substance use disorders (SUDs). Thirty studies involved interventions targeting abstinence from drug use using experimental designs where effects on treatment outcome could be attributed to the VBRT intervention. The estimated average effect size (r) for those studies was 0.32 (95% CI 0.26-0.38). Analyses of variables thought to moderate VBRT effect sizes revealed that more immediate voucher delivery and greater monetary value of the voucher were associated with larger effect sizes. Additional studies were identified wherein VBRT was used to target clinic attendance (n = 6) or medication compliance (n = 4). VBRT studies targeting attendance produced average effect sizes of 0.15 (95% CI 0.02-0.28), while those that targeted medication compliance produced an average effect of 0.32 (95% CI 0.15-0.47). No significant moderators were identified for these 10 studies. Overall, VBRT generated significantly better outcomes than did control treatments. These results further support the efficacy of VBRT, quantify the magnitude of its effects, identify significant moderators and suggest potential directions for future research.
Article
Previous studies by our group have used money given contingent on abstinence to reduce drug use by individuals with schizophrenia. In this study, we examined the sensitivity of marijuana use by individuals with serious mental illness to voucher-based contingent reinforcement, which represents the first study to date investigating the efficacy of voucher incentives with this population. This within-subject reversal design consisted of three conditions: 4-week baseline, 12-week voucher intervention, and 4-week baseline. During baseline periods, subjects received 10 US dollars vouchers per urine specimen, independent of urinalysis results. During voucher intervention, only specimens testing negative for marijuana earned vouchers, with total possible earnings of 930 US dollars. Seven adults with schizophrenia or other serious mental illnesses participated in the study. The percentage of marijuana-negative specimens was significantly greater during voucher intervention than during baseline periods. These results provide evidence that marijuana use among individuals with serious mental illness is sensitive to voucher-based incentives and further support the potential feasibility of using voucher-based contingency management to reduce substance abuse in this challenging population.
Article
Alcohol abuse in patients with schizophrenia is associated with psychiatric and social complications. While two medications have been approved by the Federal Drug Administration (FDA) for the treatment of alcoholism: disulfiram and naltrexone, no medications have been approved for individuals with alcohol dependence and comorbid schizophrenia. The purpose of this study was to evaluate the efficacy of naltrexone in alcohol-abusing schizophrenic patients. Thirty-one patients with schizophrenia and comorbid alcohol abuse or dependence were treated for 12 weeks in an outpatient study using naltrexone or placebo in a randomized, double-blind fashion in addition to their neuroleptic medication. Patients also participated in a weekly therapy using cognitive-behavioral drug relapse prevention strategies combined with skills training. Outcomes included drinking measured by the time line follow-back method, craving using the Tiffany Craving Questionnaire, psychotic symptoms using the Positive and Negative Symptoms Scale (PANSS), side effects and a measures of abnormal involuntary movements. There were no significant differences in treatment exposure or medication compliance between groups. Naltrexone treated patients had significantly fewer drinking days, heavy drinking days (>5 drinks) and reported less craving compared to the placebo treated patients. Naltrexone did not affect symptoms of schizophrenia, such as psychosis. The medication was well tolerated and there were no group differences in side effects. These data suggest that naltrexone may be an effective medication for individuals with comorbid alcohol dependence and schizophrenia. Given the widespread problems associated with alcohol misuse in this population, and the lack of effective pharmacotherapies, these findings represent an exciting clinical development.