cognitive behavioral treatment in clinically referred chronic insomniacs: group versus individual...
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Cognitive Behavioral Treatmentin Clinically Referred ChronicInsomniacs: Group VersusIndividual TreatmentIngrid H. Verbeek , Gerdy M. Konings , Albert P.Aldenkamp , August C. Declerck & Ed C. KlipPublished online: 07 Jun 2010.
To cite this article: Ingrid H. Verbeek , Gerdy M. Konings , Albert P. Aldenkamp ,August C. Declerck & Ed C. Klip (2006) Cognitive Behavioral Treatment in ClinicallyReferred Chronic Insomniacs: Group Versus Individual Treatment, Behavioral SleepMedicine, 4:3, 135-151, DOI: 10.1207/s15402010bsm0403_1
To link to this article: http://dx.doi.org/10.1207/s15402010bsm0403_1
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Cognitive Behavioral Treatment in
Clinically Referred Chronic Insomniacs:
Group Versus Individual Treatment
Ingrid H. Verbeek, Gerdy M. Konings,
Albert P. Aldenkamp, and August C. Declerck
Center for Sleep and Wake Disorders Kempenhaeghe
Heeze, The Netherlands
Ed C. Klip
Department of Medical Psychology
Groningen Academic Hospital
Groningen, The Netherlands
In this study, we compared the effect of group and cognitive behavioral treatment
(CBT) in clinically referred patients with chronic insomnia. The participants were 32
individually treated primary insomniacs and 74 individuals with either primary or
secondary insomnia treated in a group (5–7 patients per group). The primary out-
come measures were subjective sleep, quality of life (QOL), and psychological
well-being. CBT produced significant changes in sleep onset latency, total sleep
time, sleep efficiency, and wake after sleep onset. For total sleep time and sleep effi-
ciency, the improvements were maintained at follow-up as well. In the question-
naires, significant improvements from treatment were seen for the Sickness Impact
Profile, Sleep Evaluation Form, and Dysfunctional Beliefs and Attitudes About
Sleep. All these improvements remained significant at follow-up. We conclude that
CBT for insomnia is effective for both individual and group treatment. Improvements
were seen in subjective sleep parameters, QOL, attitudes about sleep, and sleep eval-
uation in general, both posttreatment and at follow-up.
In the last decade, behavioral treatment strategies have been established as a sub-
stitute or support for pharmacological treatment in insomnia (Chesson et al., 1999;
BEHAVIORAL SLEEP MEDICINE, 4(3), 135–151
Copyright © 2006, Lawrence Erlbaum Associates, Inc.
Correspondence should be addressed to Ingrid H. Verbeek, Center for Sleep and Wake Disorders
Kempenhaeghe, Sterkselseweg 65, 5590 AB, Heeze, The Netherlands. E-mail:
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Edinger & Wohlgemuth, 1999; Espie, 1991; Hauri, 1997; Morin, 1993; Oosterhuis
& Klip, 1993, 1997; Verbeek, Schreuder, & Declerck, 1999). These behavioral
techniques include sleep information, sleep hygiene guidelines, relaxation, stimu-
lus control, sleep restriction, and cognitive techniques. The format of treatment
may vary from individual to group or even self-help treatment. In addition to its
cost effectiveness, group therapy has several advantages. First, it provides the op-
portunity for patients to share a problem with fellow patients. Second, model pa-
tients may be strong allies of the therapist in convincing other patients to comply
with the prescribed regime. It is not always possible or desirable to treat insomnia
patients in a group. Some patients may simply prefer individual treatment, or the
clinician may decide that a patient’s individual psychopathology is severe enough
that it would interfere with the group process. Several studies have been published
on the results of group therapy for insomnia. A meta-analysis of 59 outcome stud-
ies that used a group design showed that nonpharmacological interventions pro-
duce reliable and durable changes in the sleep patterns of patients with chronic in-
somnia (Morin, Culbert, & Schwartz, 1994). Oosterhuis and Klip evaluated the
effect of group therapy on chronic insomniacs in primary care. The therapy was
implemented as a course consisting of eight meetings. A group of 27 people who
followed the course was compared with a wait-list control group of 17 people.
Quality of sleep increased significantly in the experimental group. Espie, Inglis,
Tessier, and Harvey (2001) found that group cognitive behavioral treatment (CBT)
offered by primary care nurses instead of clinical psychologists was found to be an
effective treatment for insomnia. Backhaus, Hohagen, Voderholzer, and Riemann
(2001) showed long-term effectiveness in group CBT of six weekly sessions. After
therapy, patients improved their total sleep time and sleep efficiency and reduced
their sleep latency, depression scores, and negative sleep-related cognitions. Re-
cently, a comparison between individual, group, and telephone consultation
showed that there were no significant differences across these three methods of
treatment implementation (Bastien, Morin, Ouellet, Blais, & Bouchard, 2004).
Unfortunately, there were no quality-of-life (QOL) parameters in these studies.
Assessment of QOL may provide important information regarding the actual se-
verity and functional limitations of insomnia, as well as the value of its treatment.
One generally accepted definition of QOL is “the functional impact of an illness
and its consequent therapy upon the patient, as perceived by the patient” (Schipper,
Clinch, & Powell, 1990). Idzikowski (1996) reported the following domains:
physical (ability to conduct activities of daily living), psychological (emotional
problems), and social (interactions with family, friends, and community). Insom-
nia affects all three of these domains. In spite of several attempts to develop a con-
dition-specific QOL measure for insomnia, none has been well validated and
widely used. The coexistence of insomnia with mood disorders and numerous
other health and environmental conditions adds to the challenge of developing a
QOL measure for insomnia (Reimer & Flemons, 2003). A study by Zammit,
136 VERBEEK ET AL.
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Weiner, Damato, Sillup, and McMillan (1999) showed that significant QOL im-
pairments are associated with insomnia. Individuals were recruited through media
advertisements, and data were obtained from individuals with insomnia and from
individuals without sleep complaints (controls). The insomnia group reported
greater impairments on specific QOL domains of the Short-Form Health Survey
(SF–36; Ware & Sherbourne, 1992). No differences were found between partici-
pants receiving pharmacological treatment for insomnia and those who were un-
treated. The influence of CBT on QOL and psychological well-being in connec-
tion with insomnia has not been carefully investigated, and previous articles often
lacked follow-up data. Verbeek, Sweere, and Klip (2005) found improvements in
QOL in individually treated patients (fewer problems with work, improved alert-
ness, more social interactions, and more recreational activities). The improve-
ments were maintained at 6- and 12-month follow-ups. Few data are currently
available about the effect of group treatment on QOL.
The vast majority of insomnia studies has been carried out on participants re-
cruited through media ads. To date, only a few clinical studies have been performed
onpatients seeking treatment inclinical settings.This is important becauseevidence
based on psychometric measures and daytime alertness shows that recruited partici-
pants may not be representative of insomniacs seeking medical attention. Physi-
cian-referred participants with chronic insomnia had higher scores in the pathologi-
cal range on psychometric measures than self-referred participants (Stepanski,
Koshorek, Zorick, Glinn, Roehrs, & Roth, 1989). In his review of the efficacy of
nonpharmacological treatment of chronic insomnia, Morin (Morin, Hauri, et al.,
1999)described that additionaloutcomeresearch isneeded toexamine theeffective-
ness of treatment when it is implemented in clinical settings. Martin and Ancoli-Is-
rael (2002) found significant differences between clinic-based and research-based
studies in the screening assessments, exclusion criteria, and participant drop-out
rate. This heterogeneity in assessment and diagnosis makes cross-study participant
comparisons challenging. They advised replicating in clinical practice the interven-
tions that were carried out in research settings. The value of our study lies in the fact
that it concerns clinically referred patients, and we included QOL parameters.
Theaim of this studywas toevaluate the short- and long-term effectsof groupand
individual CBT in clinically referred patients with chronic insomnia. The primary
outcome measures were subjective sleep, QOL, and psychological well-being.
METHOD
Participants
The participants for individual treatment were 32 chronic primary insomniacs (20
females, 12 males). These participants participated in a study in 1999 that analyzed
CHRONIC INSOMNIACS 137
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the effects of short-term CBT on subjective sleep and QOL in primary insomniacs
without regular use of hypnotics. From 2000, we switched to group therapy; from
that time on, individual treatment was offered only according to the following ex-
clusion criteria. We did not use these individually treated patients in the analyses.
Group treatment included both primary and secondary insomniacs. The partici-
pants for group treatment were 74 chronic insomnia patients (45 females, 29
males) divided over 12 groups (5–7 participants per group). Analyses were made
only for patients who had usable sleep log and questionnaire data at all four mea-
surement times: (a) baseline, (b) postwait-list, (c) after therapy, and (d) 9 months
after therapy. For group treatment and for individual treatment, 40 patients and 18
patients, respectively, had usable data for sleep logs and questionnaires according
to these criteria. All patients were referred to a specialized sleep center by their
general practitioner or specialist and had a primary complaint of insomnia. They
all received a sleep questionnaire that included medical history and a sleep log for
a 2-week period. All patients were screened by a physician for medical history and
sleep history. As needed, polysomnography according to the international criteria
(American Sleep Disorders Association, 1997, 1995) was performed. We only in-
cluded insomniacs without organic sleep disorders. Inclusion criteria were (a) pri-
mary symptom of insomnia defined as having, on at least 4 nights per week, symp-
toms of a sleep onset latency and/or wake after sleep onset of at least 30 min and a
sleep efficiency of no more than 85%; (b) negative effect during waking hours
(e.g., fatigue, impaired functioning, mood disturbances) attributed to insomnia; (c)
insomnia duration of at least 0.5 years; and (d) indication for CBT (bad sleep hy-
giene and/or dysfunctional sleep habits and/or dysfunctional thoughts about
sleep). Exclusion criteria (a) present psychopathology as determined by the psy-
chological interview with a potentially interfering effect on group therapy (e.g., se-
vere depression or burn-out; n = 66). For individual treatment, exclusion was based
on the Symptom Check List (SCL–90) scores of anxiety (score above 22 for men,
above 27 for women) and depression (above 34 for men, above 42 for women; n =
73); (b) patients who refused group therapy (only for group therapy; n = 8); (c) reg-
ular use of hypnotics (greater than or equal to 3 nights a week) and the use of anti-
depressants or over-the-counter medication (only for individual therapy; n = 39).
All patients participated voluntarily in the study, and none were paid or had to pay
for their participation.
Treatment
All participants underwent CBT, psychoeducation, sleep hygiene, stimulus control,
sleep restriction, relaxation exercises, and cognitive restructuring. Sleep restriction
is designed to consolidate sleep. The essential features of this intervention are an ini-
tial reduction in time spent in bed, followed by a gradual and slow extension of time
in bed that begins once sleep is consolidated. The instructions for stimulus control
138 VERBEEK ET AL.
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are based on the principle of classical conditioning and are designed to strengthen
the bed as a cue for sleep while weakening it as a cue for activities that are incompati-
ble with sleep (only go to bed when sleepy, use the bed only for sleep, get out of bed
when unable to sleep, wake up at the same time regardless of how much you slept).
Both group and individual treatment contained six consecutive weekly sessions
(each group session lasted 2.5 hr; each individual session lasted 1 hr). The length of
the group sessions was much longer compared with the individual sessions because
for each participant, homework was discussed. Of course, this takes more time in a
group. The content of therapy was the same in both treatments. Follow-up sessions
wereplanned1,3, and6monthsafter thesixth therapysession.Asession-by-session
overview of the treatment protocol is presented in Table 1.
Measures
Sleep logs that were maintained for 1 week (except for 2 at baseline) as well as
questionnaires were examined at four different times: (a) at baseline, (b) just be-
fore the start of treatment after a waiting period (1–3 months), (c) posttreatment,
and (d) follow-up. Patients did not have to fill in questionnaires at baseline if group
therapy began within 1 month after their first clinical interview. The main outcome
measures for the sleep log were sleep onset latency, total sleep time, sleep effi-
ciency, wake after sleep onset, and number of times awake. The data from the sleep
logs consisted of the means of 7 consecutive nights.
An index of QOL was derived from selected items of two validated question-
naires: the Sickness Impact Profile (SIP; Bergner, Bobbitt, Pollard, Martin, &
CHRONIC INSOMNIACS 139
TABLE 1Outline of Insomnia Treatment Protocol
Session Treatment
1 Program overview; acquaintance; general information about insomnia; goal
setting; sleep hygiene
2 Behavioral component (stimulus control and sleep restriction); relaxation
(Jacobson)
3 Behavioral and cognitive components (cognitive restructuring); medication
withdrawal
4 Behavioral and cognitive components; relaxation (Schultz); medication
withdrawal
5 Review of all therapy components; programming generalization of newly learned
skills; thought stopping
6 Evaluation; identification of high-risk situations; review of relapse prevention
strategies; further consolidation of therapeutic gains
Follow up (3x) Consolidation of therapeutic gains; discussing problems. Follow-up 1: 1 month
after sixth session; Follow-up 2: 3 months after Follow-up 1; Follow-up 3: 6
months after Follow-up 2
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Gilson, 1976; Luttik et al., 1987) and the RAND–36 (Brazier et al., 1992; Van der
Zee & Sanderman, 1993). To limit the number of questions, we excluded items
with little relevance for chronic insomnia (e.g., items that dealt with physical limi-
tations like mobility). Because we only used the questionnaires to compare out-
come before and after treatment, we think this choice is justified, although no anal-
yses of internal consistency are done. The SIP has three subscales: social
interactions (range = 0–20), alertness/intellectual functioning (range = 0–10) and
recreation (range = 0–8). The sum score of SIP subscales ranges from 0 to 38; the
lower the score, the better. The RAND–36 is the validated Dutch version of the
MOS SF–36 (Ware & Sherbourne, 1992). With the same rationale as the SIP, we
used only four subscales of the RAND–36: general health (range = 1–5), problems
at work (range = 5–10), social occupation (range = 1–5) and feeling (range =
9–54). The sum score of the SF–36 subscales ranges from 16 to 74; the higher the
score, the better.
Sleep was subjectively evaluated with a Sleep Evaluation Form (SEF), devel-
oped by our center and based on Morin’s Sleep Impairment Index (Morin, 1993).
The SEF has six items: satisfaction with sleep, coping with bad sleep, concerns
about sleep, tiredness, concentration, and mood. All scores range from 1 to 5. The
sum score of SEF ranges from 6 to 30; the higher the score, the better.
Psychological well-being was evaluated with SCL–90 (Arrindell & Ettema,
1986). From the SCL–90, five subscales were selected: anxiety (10 items, range
= 10–50), depression (16 items, range = 16–80), somatization (12 items, range =
12–60), insufficiency (9 items, range = 9–45), and sensibility (18 items, range =
18–90). The sum score of SCL–90 ranges from 65 to 325; the lower the score,
the better.
Beliefs and attitudes about sleep were assessed with an abbreviated version of
the Dysfunctional Beliefs and Attitudes About Sleep scale (DBAS; Morin, 1993).
Patients complete the DBAS by indicating whether they agree with the statements
in the DBAS that express dysfunctional ideas about sleep. The DBAS has five
subscales: unrealistic expectations about sleep (2 statements), beliefs about con-
trol over sleep (7 statements), beliefs about the consequences of insomnia (6 state-
ments), beliefs about the causes of insomnia (1 statement), and beliefs about
sleep-promoting habits (7 statements). The sum score of DBAS ranges from 23 to
115; the lower the score, the better.
Characteristic coping behavior was assessed with the Utrecht Coping List (UCL;
Schreurs, van de Willige, Tellegen, & Brosschot, 1996). The UCL measures coping
behavior when a person is confronted with problems or events that need adjustment.
The questionnaire contains seven subscales: active tackling (7 items, range = 7–28),
palliative reaction (8 items, range = 8–32), avoidance (8 items, range = 8–32), seek-
ing social support (6 items, range = 6–24), depressive reaction (7 items, range =
7–28), expression of emotions (3 items, range = 3–12), and reassuring thoughts (5
items, range = 5–20). The sum score of the UCL ranges from 44 to 176.
140 VERBEEK ET AL.
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Patient characteristics like age, gender, level of education (low = primary edu-
cation, middle = secondary education, high = higher education), employment sta-
tus (employed, homemaker, sick, retired), and use of medication were all recorded.
Statistics
Analyses were only made for the subgroup of patients with data on all four measure-
ment times (n = 18 individual treatment, n = 40 group treatment). Chi-square analy-
ses were conducted for categorical variables, and t tests (or analyses of variance
[ANOVAs]) were conducted for continuous variables. Chi-square analysis was per-
formed between both groups for demographic data. The level of significance of all
analyses was set at p ≤ .05. A mixed-model ANOVA with repeated measures was
used to determine variances over time for the whole group, between the two groups
(individual and group therapy), and interaction of group over time. Post-hoc analy-
ses following significant effects was performed with Bonferroni corrections.
RESULTS
Demographic data are given in Table 2. The mean ages were 43.68 years for indi-
vidually treated patients and 45.11 years for patients treated in a group (Table 2).
The percentages of women were 56% (individual) and 60% (group). The mean du-
rations of insomnia were 17.92 years (individual) and 11.96 years (group). The
percentages of highly educated patients were 56% (individual) and 30% (group).
The percentages of patients with a middle level of education were 33% (individ-
ual) and 35% (group). The percentages of patients with a low level of education
were 11% (individual) and 23% (group). The percentages of patients who were
employed were 78% (individual) and 68% (group). No significant differences
were seen between individually treated patients and patients treated in a group for
age, gender, duration of insomnia, education, and employment status. At baseline,
13 (33%) of the patients treated in a group and 6 (33%) individually treated pa-
tients took no medication. Twenty-two (55%) of the patients treated in a group and
9 (50%) individually treated patients took hypnotics. The subgroup of patients
with data on all four measurement times was different only from the larger sample
in the number of patients that took no medication (50% in larger sample, 33% in
subgroup). Tables 3 through 5 show the results from the sleep logs and question-
naires. Analyses were made only for the group of patients with data at all four mea-
surement times. Figure 1 shows total sleep time; Figure 2 shows DBAS over time.
Sleep Logs
As measured by the sleep logs, there was a significant Time effect for sleep on-
set latency, F(3, 57) = 11.88, p = .000; total sleep time, F(3, 56) = 9.87, p = .000;
CHRONIC INSOMNIACS 141
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sleep efficiency, F(3, 56) = 32.74, p = .000; and wake after sleep onset, F(3, 56)
= 9.17, p = .000 (Table 4). Post-hoc analyses (with Bonferroni corrections for
multiple comparisons) for the factor Time showed significant improvements af-
ter therapy compared to postwait-list for sleep onset latency (p = .013), total
sleep time (p = .002), sleep efficiency (p = .000), and wake after sleep onset (p =
.000). For sleep onset latency and sleep efficiency, significant improvements
were also seen from baseline to postwait-list (p = .021 and p = .029, respec-
tively). For total sleep time and sleep efficiency, follow-up data were also signif-
icantly improved compared to postwait-list (p = .003 and p = .000, respectively;
Table 3, Figure 1). There was no significant Group effect (Table 4). Only for
wake after sleep onset, there was a modestly significant Group × Time effect,
F(3, 56) = 2.68, p = .049.
Despite these significant effects in subjective sleep parameters, the percentages
of good sleepers posttreatment (according to the definition of sleep onset latency
142 VERBEEK ET AL.
TABLE 2Demographic Data for Patients With Data on All Four Measurement Times
M ± SD
Demographic Data Groupa Individualb
Age 43.68 ± 10.10 45.11 ± 11.15
Gender 24 female, 16 male 10 female, 8 male
Duration of insomnia (years) 11.96 ± 12.16 17.92 ± 15.38
% n % n
Education
High 30 12 56 10
Middle 35 14 33 6
Low 23 9 11 2
Unknown 13 5 0 0
Employment status
Employed 68 27 78 14
Homemaker 10 4 17 3
On sick leave 18 7 6 1
Student 2 1 0 0
Unknown 2 1 0 0
Medication
None 33 13 33 6
Hypnotics 55 22 50 9
Anxiolytics 3 1 11 2
Antidepressants 8 3 0 0
Over-the-counter 0 0 6 1
Unknown 3 1 0 0
an = 40. bn = 18.
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TAB
LE3
Sle
epLo
gsat
Bas
elin
e(A
),P
ostW
ait-
List
(B),
Pos
ttrea
tmen
t(C
),an
dF
ollo
wU
p(D
)fo
rP
atie
nts
With
Dat
aon
All
Fou
rM
easu
rem
entT
imes
A:
Ba
seli
ne
B:
Po
st
Wa
it-L
ist
C:
Postt
reatm
ent
D:
Foll
ow
Up
Gro
up
Indiv
idual
Gro
up
Indiv
idual
Gro
up
Indiv
idual
Gro
up
Indiv
idual
Sle
ep
Log
Param
ete
rs
MSD
MSD
MSD
MSD
MSD
MSD
MSD
MSD
SO
L(i
nm
inute
s)
68.6
958.0
456.7
748.5
849.5
334.4
244.1
546.7
840.3
131.0
323.9
324.8
042.4
130.3
829.4
426.7
8
TS
T(i
nm
inute
s)
324.3
160.4
4316.7
179.3
4323.6
963.0
3323.0
180.1
2345.0
572.9
0367.3
368.0
8357.1
581.8
1367.0
581.4
0
SE
(%)
62.4
513.4
461.9
914.8
069.1
512.3
265.4
916.7
977.4
713.0
180.2
413.4
374.4
412.0
075.5
816.6
1
WA
SO
(in
min
ute
s)
58.9
545.2
763.5
844.7
148.7
344.6
969.5
656.0
539.1
830.3
332.9
926.0
344.2
336.0
661.3
655.5
7
AW
AK
(no.)
1.2
90.9
41.5
51.1
21.1
40.9
91.4
40.9
01.2
50.8
71.2
91.1
01.2
80.9
81.5
00.9
5
No
te.
Gro
up
treatm
ent(n
=40);
indiv
idualtr
eatm
ent(n
=18).
SO
L=
sle
ep
onsetla
tency;T
ST
=to
talsle
ep
tim
e;S
E=
sle
ep
eff
icie
ncy;W
AS
O=
wake
aft
er
sle
ep
on-
set;
AW
AK
=num
ber
of
aw
akenin
gs.
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≤ 30 min, SE ≥ 85%, and total sleep time ≥ 300 min) are disappointing (34% in-
dividual and 16% group treatment).
Questionnaires
Table 5 and Figure 2 show the sum scores for the various questionnaires. QOL im-
proved significantly for the whole group after therapy. There was a significant Time
effect for both QOL questionnaires: SF–36, F(3, 31) = 10.60, p = .000, and SIP, F(3,
33) = 8.85, p = .000; the SEF, F(3, 333) = 55.00, p = .000; the SCL–90, F(3, 29) =
6.80, p = .000; and the DBAS, F(3, 33) = 41.43, p = .000 (Table 4). Post-hoc analyses
(with Bonferroni corrections for multiple comparisons) for the factor Time showed
significant improvements from baseline to postwait-list for SF–36 and SEF. Signifi-
cant improvements from postwait-list to after therapy and for postwait-list to fol-
low-up were seen for SIP (p = .000 and p = .025, respectively), SEF (p = .000 and p =
.000, respectively), and DBAS (p = .000 and p = .000, respectively; Table 5, Figure
2). Again, there was no significant Group effect. A significant Group × Time effect
was seen for the SEF scores, F(3, 33) = 4.93, p = .003.
DISCUSSION
The findings presented here complement previous studies showing that CBT is an
effective treatment for chronic primary insomnia (Edinger, Wohlgemuth, Radtke,
Marsh, & Quillian, 2001a; Espie, Inglis, Tessier, & Harvey, 2001; Morin,
144 VERBEEK ET AL.
TABLE 4Mixed Model Analysis of Variance Results for Sleep Log and
Questionnaires
Mixed Model Effects
Domain Time Interactiona Group × Timea Groupb
Sleep onset latency 11.88*** 0.45 1.98
Total sleep time 9.87*** 0.90 0.13
Sleep efficiency 32.74*** 1.10 0.00
Wake after sleep onset 9.17*** 2.68* 0.83
SF–36 10.60*** 1.53 0.44
Sickness Impact Profile 8.85*** 0.08 2.21
Sleep Evaluation Form 55.00*** 4.93** 0.00
SCL–90 6.80*** 0.35 0.21
DBAS 41.43*** 0.99 0.12
Note. n = 40, for group; n = 18, for individual. SF–36 = social functioning; SCL–90 = Symptom
Check List; DBAS = Dysfunctional Beliefs and Attitudes About Sleep.
adf = 3. bdf = 1.
*p < .05. **p < .01. ***p < .001.
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TAB
LE5
Que
stio
nnai
res
atB
asel
ine
(A),
Pos
tWai
t-Li
st(B
),P
osttr
eatm
ent(
C),
and
Fol
low
Up
(D)
for
Pat
ient
sW
ithD
ata
onA
llF
our
Mea
sure
men
tTim
es
A:
Ba
seli
ne
B:
Po
st
Wa
it-L
ist
C:
Postt
reatm
ent
D:
Foll
ow
Up
Gro
up
Indiv
idual
Gro
up
Indiv
idual
Gro
up
Indiv
idual
Gro
up
Indiv
idual
Questi
onnair
es
(Min
–M
ax)
Sum
SD
Sum
SD
Sum
SD
Sum
SD
Sum
SD
Sum
SD
Sum
SD
Sum
SD
SF
–36
(16–74)
44.2
56.6
147.3
47.8
947.2
88.1
251.6
97.7
153.1
59.1
855.7
29.6
253.2
98.0
555.1
49.2
4
SIP
(0–38)
10.6
75.1
28.4
75.4
99.7
05.3
17.8
94.7
46.3
55.0
34.5
94.5
36.3
84.9
64.6
15.5
4
SE
F(6
–30)
13.6
72.0
614.0
33.0
015.2
12.6
714.6
42.7
319.2
82.9
920.8
12.9
320.1
02.6
620.7
54.6
8
SC
L–90
(65–325)
112.4
027.7
2108.3
525.2
8113.2
134.5
298.0
219.0
197.7
827.5
394.1
127.1
897.6
122.5
595.6
126.0
4
DB
AS
(23–115)
67.4
511.4
770.7
113.5
463.5
613.6
465.5
612.0
148.0
510.1
546.3
310.9
946.7
011.8
849.7
815.6
9
CO
PIN
G(4
4–176)
83.2
56.8
492.4
49.5
079.4
38.6
792.5
69.9
981.0
010.1
891.3
111.0
780.5
910.1
991.2
210.0
0
No
te.
Gro
up
treatm
ent:
n=
40;in
div
idualtr
eatm
ent:
n=
18.Q
uali
tyof
life
ism
easure
dby
SF
–36
and
SIP
.Im
pro
vem
enton
SF
–36
and
SE
Fis
show
nby
hig
her
score
s.
Impro
vem
ent
on
SIP
,S
CL
–90,and
DB
AS
isshow
nby
low
er
score
s.S
F–36
=socia
lfu
ncti
onin
g;
SIP
=S
ickness
Impact
Pro
file
;S
EF
=S
leep
Evalu
ati
on
Form
;S
CL
–90
=
Sym
pto
mC
heck
Lis
t;D
BA
S=
Dysfu
ncti
onal
Beli
efs
and
Att
itudes
About
Sle
ep.
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146
FIGURE 1 Mean values for total sleep time, both for individual and group treatment. Stars
indicate time points with significant post-hoc difference (with Bonferroni corrections for multi-
ple comparisons) for the whole group (p < .01). Comparisons are made from postwait-list to af-
ter therapy and follow up. There were no significant group effects.
FIGURE 2 Mean values for Dysfunctional Beliefs and Attitudes About Sleep (DBAS), both
for individual and group treatment. Stars indicate time points with significant post-hoc differ-
ence (with Bonferroni corrections for multiple comparisons) for the whole group (p < .01).
Comparisons are made from postwait-list to after therapy and follow up. There were no
significant group effects.
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Colecchi, et al., 1999). In our analysis, the comparison of postwait-list to after ther-
apy and follow-up is most interesting because these comparisons reflect the
changes that can be attributed to treatment. These comparisons show that CBT
produced significant changes in sleep onset latency, total sleep time, sleep effi-
ciency, and wake after sleep onset. For total sleep time and sleep efficiency, signifi-
cant improvements were seen at follow-up as well. Sleep onset latency and sleep
efficiency already improve during the waiting time. This can be due to the fact that
some patients already received some sleep hygiene advice after the first interview.
Our study did not show different outcomes between individual and group treat-
ment. Bastien et al. (2004) also showed that individual and group treatments are
equallyeffective.Thereareafewadvantagesofgrouptreatment thatarenotshownin
the results, however. First of all, group treatment is cost effective. Although the
group sessions took longer (2.5 hr) compared to individual treatment (1 hr), group
treatment is cost effective by3 participants per group. There is another, perhaps even
more important advantage of group treatment. After the 6-week program, written
evaluations were completed by the patients treated in a group. The most frequent an-
swer to the open question, “What part of the sleep course was most helpful for you?,”
was the behavioral component (sleep restriction and stimulus control). “Cognitive
restructuring” was mentioned second most frequently, and “meeting with other peo-
plewith insomnia”wasmentionedthirdmost frequently(e.g.,moreoften thanrelax-
ationexercises). Ingroup treatment, there is theopportunitytomeetotherchronic in-
somniacs, and it is evident that this is appreciated by the participants.
The different selection criteria between group and individually treated patients
may be a possible explanation for the higher percentage of good sleepers after ther-
apy in individually treated patients compared to patients treated in a group. Only in
the individually treated patients were there exclusion criteria for secondary insom-
nia and the regular use of hypnotics. Another explanation may be that patients for
whom individual treatment was not successful were excluded for follow-up be-
cause of other treatment (e.g., antidepressants). This is confirmed by the finding
that the patients with no data for at least one of the four measurement times (n = 13;
all patients did not have follow-up data) had significantly lower total sleep time
and sleep efficiency at baseline than the group with data at all measurement times
(n = 18). Morin (2003) recently described the need to broaden the scope of out-
come assessment beyond the simple reduction of insomnia symptoms as seen in
the sleep parameters. Effective treatment should also produce clinically meaning-
ful changes in daytime functioning, fatigue, mood, and QOL. The results of our
study show significant improvements in QOL and psychological well-being after
treatment. Again, there was no significant effect between individual and group
treatment. Most of these changes were maintained at follow-up. No significant
changes in coping on the UCL were seen either posttreatment or at follow-up. The
UCL measures characteristic coping behavior when confronted with problems or
events that need adjustment. Specific coping with insomnia is not measured with
CHRONIC INSOMNIACS 147
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this list. This may explain why we did not find any significant improvements in this
list. The changed beliefs and attitudes about sleep as seen in the DBAS make it
likely that CBT leads to a different attitude and experience of sleep. Edinger et al.
(2001b) also found that CBT is effective for reducing dysfunctional beliefs about
sleep. In their study, the improvements were significantly correlated with improve-
ments on both objective and subjective measures of insomnia symptoms.
Thus, CBT improves not only sleep, but also general well-being and QOL. This
finding is in contrast with that of Zammit et al. (1999), who found no differences in
QOL between participants who received pharmacological treatment for insomnia
versus those who did not. Both studies are hard to compare because their patients
received pharmacological treatment instead of CBT and were recruited instead of
clinically referred. Stepanski et al. (1989) found that physician-referred partici-
pants had higher scores on the pathological range on all psychometric parameters
than those who were self-referred. It is an interesting finding that, in our clinically
referred patients, improvements were seen in daytime functioning (psychological
well-being, QOL, sleep evaluation in general). This is in contrast with the study by
Means, Lichstein, Epperson, and Johnson (2000), where the effect of progressive
relaxation led to improvements in sleep but not to improvements in daytime func-
tioning. Perhaps the behavioral and cognitive elements of CBT are crucial in ob-
taining these daytime improvements. Recent literature confirms that the critical el-
ements for CBT are reported home use of stimulus control, sleep restriction, and
cognitive restructuring (Harvey, Inglis, & Espie, 2002). Besides differences in
QOL, there are more changes between recruited and clinically referred patients.
The recruited patients from the studies of Morin, Colecchi, et al. (1999) and
Edinger et al. (2001a) reflect an older patient population. The mean ages of our pa-
tients were 45.1 years (individual treatment) and 43.7 years (group treatment)
compared to 64.4 years (Morin, Colecchi, et al., 1999) and 55.3 years (Edinger et
al., 2001a). The mean ages of onset of sleep complaints in our population ranged
from 27.2 to 31.7 years, compared to 42 to 48 years in the recruited participant
studies mentioned before. It is well known that sleep deteriorates with age. Even
without the correction for age, our patients experienced subjectively worse sleep
than the recruited patients from the literature studies mentioned previously. When
looking at the demographic data, no significant differences were seen in age, gen-
der, education, or duration of insomnia between individually treated patients and
patients treated in a group. The percentage of patients with a high level of educa-
tion was much higher in individual therapy (46.9% compared to 27.0% in group
therapy). This was not significant, however. Compared to individual treatment,
significantly more patients in group treatment took hypnotics at baseline. In the
subgroup of patients for which the analyses were made, however, no significant
difference was seen between hypnotic usage and no usage at baseline. Espie,
Inglis, and Harvey (2001) already found that patients using hypnotics respond
equally well to CBT.
148 VERBEEK ET AL.
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The limitations of our study lie in the fact that there was no randomization for
individual or group treatment and that the criteria for allocation to group or indi-
vidual treatment were different. The individually treated patients in this analysis
were primary insomniacs and no regular users of hypnotics. The fact that there
were no significant changes between group and individual treatment, even though
the selection criteria were different, supports the finding that both treatment mo-
dalities have comparable effects. Bastien et al. (2004) also found no difference be-
tween group and individual treatment. Another limitation of our study lies in the
fact that there was no control group. Although we had a waiting-list control, there
were already some significant improvements from baseline to postwait-list (sleep
onset latency, sleep efficiency, SF–36, and SIP). These improvements may be ex-
plained from the sleep hygiene advice patients already received after the first inter-
view. Short-term CBT, however, adds more significant improvements in subjective
sleep, QOL, and psychological well-being.
We conclude that CBT for insomnia is equally effective for both individual and
group treatment. Improvements was seen in subjective sleep parameters, QOL, at-
titudes about sleep, and sleep evaluation in general, both posttreatment and at fol-
low-up. Group CBT has two extra advantages: It allows participants to meet fellow
patients, and it is cost effective.
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