Vvpt.be
Eur Child Adolesc Psychiatry (2007)16:157–167 DOI 10.1007/s00787-006-0584-x
ORIGINAL CONTRIBUTION
Childhood depression: a place for
Ilan JoffeJesse Campbell
Carmen ClementeFredrik Almqvist
An outcome study comparing individual psychodynamic
psychotherapy and family therapy
Ulla Koskenranta-AaltoSheila WeintraubGerasimos KolaitisVlassis TomarasDimitris AnastasopoulosKate GraysonJacqueline BarnesJohn Tsiantis
j Abstract Background
disorder rates were seen for both
Accepted: 14 October 2006Published online: 2 January 2007
Although considered clinically
Individual Therapy and Family
effective, there is little systematic
Therapy. A total of 74.3% of cases
Original lead researcher: Prof Issy Kolvin
research confirming the use of
were no longer clinically depressed
Individual Psychodynamic Psy-
following Individual Therapy and
chotherapy or Family Therapy as
75.7% of cases were no longer
J. Trowell, MBBS, DCH, DPM, FRCPsych
treatments for depression in chil-
clinically depressed following
(
&)Professor of Child Mental Health
dren and young adolescents. Aims
Family Therapy. This included
West Midlands NIMHE/CSIP
A clinical trial assessed the effec-
cases of Dysthymia and ‘‘Double
Honorary Consultant Child &
tiveness of these two forms of
Depression'' (co-existing Major
Adolescent Psychiatrist
psychotherapy in treating moder-
Depressive Disorder and Dysthy-
ate and severe depression in this
mia). There was also an overall
London NW3 5BA, UK
age group. Methods A randomised
reduction in co-morbid conditions
Tel.: 01707 652205 (UK)
control trial was conducted with 72
across the study. The changes in
patients aged 9–15 years allocated
both treatment groups were per-
I. Joffe, MRCPsych
to one of two treatment groups.
sistent and there was ongoing
Hertfordshire Partnership NHS Trust,
Results Significant reductions in
improvement. At follow up six
Child & Family Clinic
months after treatment had ended,
Marlowes Health Centre
100% of cases in the Individual
Hemel Hempstead HP1 1HE, UK
G. Kolaitis, MD
Æ D. Anastasopoulos, MDJ. Tsiantis, MD, DPM, FRCPsych
Therapy group, and 81% of cases in
Department of Child Psychiatry,
the Family Therapy group were no
Aghia Sophia Children's Hospital
longer clinically depressed. Con-
Athens University Medical School
London NW3 5BA, UK
clusions This study provides evi-
Thivon & Levadias115 27 Athens, Greece
dence supporting the use of focused
C. Clemente, MRCPsychRoyal Free Hampstead NHS Trust
forms of both Individual Psycho-
Department of Child &
dynamic Therapy and Family
Department of Psychiatry,
Adolescent Psychiatry
Eginition Hospital
Therapy for moderate to severe
Royal Free Hospital
Athens University Medical School
depression in children and young
72 Vas. Sophias Av
London NW3 3DP, UK
115 28 Athens, Greece
F. Almqvist, MD, PhD
K. Grayson, BA, MSc, FRSS
j Key words treatment –
Statistics By Design
U. Koskenranta-Aalto, MD
childhood depression –
6 Southampton Close, Blackwater
individual psychotherapy –
Camberly, Surrey G U17 0HB, UK
Department of Child Psychiatry
The Hospital for Children & Adolescents,
J. Barnes, BSc, MSc, PhD
Faculty of Medicine
Institute for the Study of Children, Families
University of Helsinki
and Social Issues, Birkbeck
University of London
00250 Helsinki, Finland
7 Bedford Square WC1B 3RA, UK
European Child & Adolescent Psychiatry (2007) Vol. 16, No. 3 Steinkopff Verlag 2007
family environment can contribute to childhooddepression Depressed children who live in a
Although considered clinically effective, there is little
confrontational environment also have higher rates of
systematic research into the efficacy of Individual
Psychodynamic Psychotherapy or Family Therapy in
There is strong evidence of an association between
the treatment of depression in children and young
depression in children and problems in family
adolescents. Most available evidence concerning
members, including dysfunctional family relation-
psychological treatments is for Cognitive Behavioural
ships ]. Factors such as high parental criticism,
Therapy (CBT) or Inter-personal Therapy []. While
family discord and poor communication between
CBT is promising in the short-term, previous studies
parent and child have been associated with the onset
, ] have found high rates of relapse, suggesting
and course of juvenile depressive disorder. Goodyer
the need for continuation or booster treatment. Psy-
et al. [] concluded that psychosocial interventions
chodynamic psychotherapy holds the promise of
with first-degree relatives and current close friend-
effecting more lasting changes in childhood depres-
ships should be considered as part of a treatment
sion by improving the capacity to resolve internal and
strategy for first episode Major Depressive Disorder in
external conflicts over time
With the serious nature of childhood/adolescent
The aim of this study was to conduct a trial of two
depression it is crucial that treatments with efficacy
established but as yet unvalidated forms of psycho-
and more than transitory effects, and with the po-
therapy for major depression in childhood/adoles-
tential for a reduction in the cumulative risks, be
provided promptly and skilfully.
Psychotherapy (‘‘Individual Therapy'') with a focus
There is some evidence to support the use of
on interpersonal relationships, life stresses and dys-
antidepressant medication in the treatment of child-
functional attachments based on the model of Malan
hood depression. Previous placebo-controlled studies
] and Davenloo who provide guidelines about
have reported response rates to Fluoxetine mono-
psychodynamics, training and techniques in brief
therapy of 52% and 56% [in cases of major
dynamic psychotherapy. (ii) Systems Integrative
depression. The TADS study reported a response
Family Therapy (‘‘Family Therapy'') with a focus on
rate of 60.6% to Fluoxetine monotherapy for Major
family dysfunction, but without specific attention to
Depressive Disorder, and 71% when Fluoxetine was
unresolved intra-psychic conflicts and early child-
combined with CBT. However, the use of Selective
hood These treatments were compared in
Serotonin Re-uptake Inhibitors in the under 18 pop-
three culturally diverse settings, using a manualised
ulation is becoming more restricted because of the
risk/benefit ratio [It is therefore important to
It was hypothesised that Individual Therapy would
identify alternative treatment modalities for depres-
be an effective treatment for depression and that
sion in children and young adolescents.
improvement would be maintained and ongoing.
While CBT has been found to be superior to
Family therapy could also be effective in the treatment
comparison interventions in the treatment of Major
of depression. Based on the findings of Brent et al. [
Depressive Disorder (MDD) in children/adolescents
which demonstrated a 37.9% response rate for
in 4 out of 6 randomised trials [], some limitations
depression with Family Therapy, it was hypothesised
have been identified: severe cases of depression
that Family Therapy might not be as effective as
have not been included, nor were cases with many co-
Individual Therapy in the treatment of depression.
morbid problems such as conduct disorder or
Further hypotheses were made with regard to the
repeated self-harm. A number of methodological
sequence of response (internal change vs social
limitations in the existing research to date were also
interaction) and predictors of response between the
identified in a review of the treatment research
two therapy groups using other measures as well as
Muratori et al. [] have shown that psychody-
changes of psychosocial functioning based on the
namic psychotherapy is effective in treating inter-
Social Adjustment Scale for Children and the Family
nalising disorders in routine outpatient care; the
Assessment Device. These will be reported in sub-
benefits of such treatment were manifest both
sequent papers.
immediately and with delayed onset (‘‘sleeper effect'').
A number of factors suggest a place for Family
Therapy in the treatment of depression in children.
Parents can be important agents for behaviouralchange, as a positive parental attitude may be a
A randomised control trial was conducted in London
powerful contributor to self-worth in childhood/ado-
(Tavistock Clinic), Athens (Aghia Sophia Children's
lescence There is now much evidence that the
Hospital) and Helsinki (Children's Hospital), with 72
J. Trowell et al.
Childhood depression: a place for psychotheraphy
patients aged 9–15 years allocated to either Individual
Kiddie-SADS ], a standardised semi-structured
Therapy (FIPP) or Family Therapy (SIFT), based on
standard randomisation methods. Caseness was the
Children had to be living with at least one bio-
only factor considered at randomisation. Patients in
logical parent, and any antidepressants or other psy-
each centre were randomly allocated to one of the two
chotropic medication had to have been stopped at
least 4 weeks prior to commencement of therapy, to
Ethical approval for the study was obtained locally
ensure the exclusion of confounding variables.
in each of the three centres. The use of placebo con-
Exclusion criteria included: depressive disorders
trols was ruled out on ethical grounds [,
meriting urgent hospitalisation, Bipolar and Schizo-
Based on previous studies of therapy with malad-
affective disorder, severe conduct disorder (consid-
justed children [, a power calculation was done
ered likely to respond only moderately to psycho-
to detect a difference in outcome of 30% between the
therapy) and parents with psychotic disorder or
two treatment groups. Accordingly, it was expected
severe personality disorder.
that 44 patients per group would be required to detect
Following screening, 24 cases entered into therapy
a 30% difference with 80% power, using a 5% test of
in each country, divided equally between therapy
significance. Following difficulties with recruitment, a
types in London and Helsinki, with 11 in Individual
further power calculation was carried out based on
therapy and 13 in Family therapy in Athens.
another review of the literature; using the Brent et al.
Treatment was conducted over a 9-month period
study [] sample size as a guide, where there were 35–
and consisted of eight to fourteen 90 min sessions of
37 subjects in each treatment arm, the size of the
Family Therapy (mean = 11), or sixteen to thirty
treatment groups in this study was adjusted accord-
50 min sessions of Individual Therapy (mean = 24.7)
plus Individual Parent sessions (one per 2 sessions of
All participants were referred into the study from
child's psychotherapy) by a separate case worker.
community Child Mental Health Services. The pa-
There were between 4 and 6 individual therapists, and
tients' progress within the study is illustrated in the
4 and 6 family therapists in each of the three centres.
CONSORT diagram [in Fig.
The therapists in Athens and Helsinki had received
Entry to the trial followed screening using the
training from the London team prior to the com-
Child Depression Inventory a brief self-report
mencement of the study. Treatment manuals were
measure. Children scoring >13 were included pro-
used to ensure comparability across all three centres,
vided they subsequently met criteria for Major
supplemented by cross-centre training.
Depressive Disorder (MDD) and/or Dysthymia on the
Assessment took place prior to treatment (‘‘Base-
line''), at the end of therapy (‘‘End of Therapy'', pri-mary endpoint) and again 6 months later (‘‘Followup'', secondary endpoint). Patients ‘‘lost to follow up''
Recruited subjects (CDI>13): 110
were those who did not return for ‘‘End of therapy'' or‘‘Follow up'' assessment. They had attended a variablenumber of therapy sessions.
Baseline assessment:
An extensive battery of instruments was adminis-
Met inclusion criteria
tered at each time point (full details available from the
authors) collecting information about the child, theparents, their families, as well as relevant schoolmeasures. The findings of the following instruments
are reported here:
1. The Demography Interview [a semi-structured
Individual therapy: 35
Family therapy: 37
2. The Kiddie-SADS [this semi-structured clinical
interview provides a measure of Major Depressive
End of therapy assessment
End of therapy assessment
Disorder and Dysthymia (based on DSM IV crite-
Lost to follow-up: 0
Lost to follow-up:
ria), and psychiatric co-morbidity. These includedanxiety disorders (Generalised, Phobias, Separa-tion anxiety and Panic disorder), behavioural dis-
Follow-up assessment
Follow-up assessment
orders (ODD, Conduct disorder), OCD, ADHD and
Anorexia nervosa.
Lost to follow-up: 0
Lost to follow-up: 1
3. The Childhood Depression Inventory (CDI)
this 27 item self-report questionnaire indicates the
Fig. 1 CONSORT diagram
European Child & Adolescent Psychiatry (2007) Vol. 16, No. 3 Steinkopff Verlag 2007
number of depressive symptoms and has a cut off
factors related to improvement in each of the therapy
indicating the presence of depression. A score of 13
was used as the threshold for entry into the study,based on research by Garvin et al. [] for use ofthe CDI in clinical settings.
4. Moods & Feelings Questionnaire (MFQ, 1): this 16
item self-report questionnaire provides a measure
j Characteristics of the sample
of depression. A threshold of 8 or more defineshigh scorers.
The mean age of participants was 12 years, almost
5. The Children's Global Assessment Scale (C-GAS,
two thirds (62%) were male, the majority were white
[]): this clinician rated scale provides a measure
and they represented all social class groups (see Ta-
of overall impairment of child functioning (range
ble Almost two thirds (62%) came from two-par-
of scores: 0 (lowest) to 100 (highest)).
ent families (although not necessarily both biologicalparents). Just under half (44%) had a history ofmaternal psychiatric illness while 15% had a historyof depression in their extended family (siblings,
j Statistical analysis
grandparents, aunts and uncles). Three quarters(76%) had been depressed for more than 6 months.
Mixed Model Repeated Measures ANOVA was used to
Overall, the sample characteristics were similar in
examine the extent of depression (as measured by the
each therapy type, except for a significantly higher
continuous instruments CDI, MFQ and C-GAS) at
percentage of males in the Individual therapy group
each of the three time points. v2 and Exact tests were
(v2 = 4.036; df = 1; P < 0.05) and a significant higher
used for the comparison of the presence/absence of
prevalence of paternal psychiatric history in the
depression using cut-offs and the Kiddie-SADS.
Due to the small sample size in each country, most
P < 0.05). A possible explanation for these findings is
of the analysis was done for the three countries
that demographic factors were not taken into con-
sideration at randomisation. These differences may
With regards to the Kiddie-SADS data, results have
have disappeared had the sample size been larger.
been calculated for separate disorders, but since theyare known to occur together it was deemed appro-priate to adjust the significance level to control for
j Prevalence of depressive disorders
this association. A significance level of P < 0.01 wasused therefore instead of P < 0.05. Also the associa-
The prevalence of cases of MDD and/or Dysthymia,
tions between these disorders are stated where
only MDD, only Dysthymia and both MDD and
applicable, and the significant results using these
Dysthymia (‘‘double depression'') have been exam-
criteria are reported.
ined. This was done to examine any differences in
There were four ‘‘lost to follow up'' cases (1 in
treatment effects in these clinically distinct groups of
Athens, 3 in London, all in the SIFT group). Inten-
tion-to-treat analysis principles were applied for thesecases, with regard to the K-SADS scores, in order not
Prevalence of Depression (Major Depressive Disorder
to weaken the power of the sample size. Last available
and/or Dysthymia) before and after therapy based on
scores were carried forward. With regard to the CDI
and MFQ, we used a ‘‘mean substitution'' method fordealing with missing data, where feasible and appro-
At baseline assessment all the participants were
priate. Means were calculated for each instrument
diagnosed as depressed, with either MDD and/or
splitting by centre, time point and therapy type and
Dysthymia, based on the Kiddie-SADS. By the end of
imputed. Analysis carried out on the pre- and post
therapy, of those receiving Individual Therapy, 74.3%
imputed data sets for each instrument confirmed that
were no longer diagnosed as depressed and none were
this did not change the statistical significance of any
diagnosed as depressed at follow up, (see Table ). Of
of the findings, other than to maintain the power of
those receiving Family Therapy, 75.7% of cases of
depression had improved by the end of therapy and at
A secondary analysis using Multi-level modelling
follow up only 18.9% were still diagnosed as de-
(ML-WIN) on the pre-imputed data was also carried
out on the CDI, MFQ and C-GAS data. The results of
The change in prevalence of depression over the 3
this (not presented here) confirmed the findings of the
time points in the Individual Therapy group, was
primary analysis. This also allowed us to examine
J. Trowell et al.
Childhood depression: a place for psychotheraphy
Table 1 Characteristics of thesamplea
Individual therapy
Standard deviation
v2 = 4.036; df = 1; P < 0.05
Socio-economic statusb
Parental marital status
Married/living with partner
Maternal psychiatric history
Paternal psychiatric history
v2 = 5.449; df = 1; P < 0.05
Depression in extended family (excluding parents)
One family member
Two family members
Duration of depressive illness
a Demography interview (Kolvin et al. 1991)
b UK Register General's Classification (Social class 1 = highest, Social Class 5 = lowest)
P < 0.001). Further 2 · 2 v2 were performed to con-
The prevalence of depression in the two groups
firm between which times points the significant
was similar at the end of therapy. At follow-up there
changes had occurred. It was found that there was a
were significantly more cases with depression in the
statistically significant change in prevalence of
Family Therapy group (v2 = 7.335; df = 1; P < 0.01).
depression from Baseline to End of Therapy
However, when the ‘‘lost to follow up'' cases were
(v2 = 41.364; df = 1; P < 0.001), from Baseline to
excluded, the prevalence of depression in the Family
Follow up (v2 = 70.00; df = 1; P < 0.001) and also
Therapy group at End of Therapy was 13.4%, and at
from End of Therapy to Follow up. (v2 = 10.328;
Follow up 8.1%. The comparison at Follow up be-
df = 1; P < 0.001).
tween the therapy types was not statistically signifi-
The change in prevalence of depression over the 3
cant when the ‘‘lost to follow up'' cases were excluded.
time points in the Family Therapy group, was alsostatistically
Prevalence of Major Depressive Disorder (MDD) before
P < 0.001). The 2 · 2 v2 performed as above found
and after therapy based on the Kiddie-SADS
that there was a statistically significant change inprevalence of depression from Baseline to End of
At the start of therapy more than 90% of the partic-
Therapy (v2 = 45.043; df = 1; P < 0.001), from Base-
ipants were diagnosed as having Major Depressive
line to Follow up (v2 = 50.455; df = 1; P < 0.001) but
Disorder (see Table By the end of therapy only 6
not from End of Therapy to Follow up.
(17.1%) still had this diagnosis in the Individual
European Child & Adolescent Psychiatry (2007) Vol. 16, No. 3 Steinkopff Verlag 2007
Table 2 Presence of Depression(Major Depressive Disorder and/or
Individual therapy N = 35
Family therapy N = 37
Dysthymia), Major DepressiveDisorder (MDD), Dysthymia, and
Double Depression (MDD andDysthymia) at three time points by
therapy type, based on the Kiddie-
SADS (percentages in brackets)
Double depression
a Including imputed data for 4 ‘‘lost to follow-up'' cases
Therapy group and by follow-up none received this
lence of MDD in the Individual Therapy group com-
diagnosis. In the Family Therapy group, the propor-
pared to the Family Therapy group at Follow up was
tion with a diagnosis of MDD had dropped from 34
not statistically significant.
(91.9%) at baseline to 8 (21.6%) at the end of therapyand 7 (18.9%) at the follow-up contact.
Prevalence of Dysthymia before and after therapy
The reduction in prevalence of MDD over the 3
based on the Kiddie-SADS
time points in the Individual Therapy group wasstatistically
At the start of therapy more than 50% of the partic-
P < 0.001). Further 2 · 2 v2 were performed to con-
ipants were diagnosed as having Dysthymia (see Ta-
firm between which time points the significant chan-
ble By the end of therapy only 6 (17.1%) still
ges had occurred. It was found that there was a
gained a diagnosis of Dysthymia in the Individual
statistically significant change in prevalence of MDD
Therapy group and by follow-up none received this
from Baseline to End of Therapy (v2 = 38.914; df = 1;
diagnosis. In the Family Therapy group, the propor-
P < 0.001), from Baseline to Follow up (v2 = 58.947;
tion with a diagnosis of Dysthymia had dropped from
df = 1; P < 0.001) but not from End of Therapy to
20 (54.1%) at baseline to 7 (18.9%) at the end of
therapy and 4 (10.8%) at the follow-up contact.
The change in prevalence of MDD over the 3 time
As shown in Table the change in prevalence of
points in the Family Therapy group was also statis-
Dysthymia over the 3 time points in the Individual
tically significant (v2 = 51.371; df = 2; P < 0.001).
The 2 · 2 v2 performed as above found that there was
(v2 = 32.308; df = 2; P < 0.001). Further 2 · 2 v2
a statistically significant change in prevalence of MDD
were performed to confirm between which time
from Baseline to End of Therapy (v2 = 37.220; df = 1;
points the significant changes had occurred. It was
P < 0.001), from Baseline to Follow up (v2 = 39.871;
found that there was a statistically significant change
df = 1; P < 0.001) but not from End of Therapy to
in prevalence of Dysthymia from Baseline to End of
Therapy (v2 = 11.993; df = 1; P < 0.005), from Base-
The prevalence of MDD in the Individual Therapy
line to Follow up (v2 = 28.00; df = 1; P < 0.001) but
group compared to the Family Therapy group at End
not from End of Therapy to Follow up.
of Therapy was not statistically significant. The
The change in prevalence of Dysthymia over the 3
prevalence of MDD in the Individual Therapy group
time points in the Family Therapy group was also
compared to the Family Therapy group at Follow up
P < 0.001). The 2 · 2 v2 performed as above found
P < 0.01). However, this difference resulted from the
that there was a statistically significant change in
inclusion of the 4 ‘‘lost to follow up'' cases in the
prevalence of Dysthymia from Baseline to End of
Family Therapy group (there were no ‘‘lost to follow
Therapy (v2 = 9.855; df = 1; P < 0.005), from Base-
up'' cases in the Individual Therapy group). When the
line to Follow up (v2 = 15.787; df = 1; P < 0.001) but
‘‘lost to follow up'' cases were excluded, the preva-
not from End of Therapy to Follow up.
J. Trowell et al.
Childhood depression: a place for psychotheraphy
The prevalence of Dysthymia in the Individual
Table 3 Mean scores for depression based on the Childhood Depression
Therapy group compared to the Family Therapy
Inventory (CDI) and the Moods & Feelings Questionnaire (MFQ), and Meanscores for the global functioning based on the C-GAS, at three time points by
group at End of Therapy was not statistically signifi-
cant. This was also the case at Follow up.
Individual therapy
Prevalence of ‘‘Double Depression'' (Major Depressive
Disorder and Dysthymia) before and after therapybased on the Kiddie-SADS
At the start of therapy 48.6% in the Individual Therapy
group and 45.9% in the Family Therapy group were
diagnosed as having double depression (see Table ).
By the end of therapy only 3 (8.6%) still gained a
diagnosis of double depression in the Individual
Therapy group and by follow-up none received this
diagnosis. In the Family Therapy group, the propor-
tion with a diagnosis of double depression had drop-
ped from 17 (45.9%) at baseline to 6 (16.2%) at the endof therapy and 4 (10.8%) at the follow-up contact.
In the Individual Therapy group, the mean drop in
As shown in Table , the change in prevalence of
CDI score from Baseline to End of Therapy was 7.77,
double depression over the 3 time points in the
with a further drop of 5.49 from End of Therapy to
Individual Therapy group was statistically significant
Follow up (Total drop: 13.26). In the Family Therapy
(v2 = 30.512; df = 2; P < 0.001). Further 2 · 2 v2
group, the mean drop in CDI score from Baseline to
were performed to confirm between which time
End of Therapy was 13.08, but with only a further
points the significant changes had occurred. It was
mean drop of 1.18 from End of Therapy to Follow up.
found that there was a statistically significant change
(Total drop: 14.26).
in prevalence of double depression from Baseline to
Secondary analysis using ML WIN confirmed the
End of Therapy (v2 = 13.720; df = 1; P < 0.001), from
above findings.
Baseline to Follow up (v2 = 22.453; df = 1; P < 0.001)but not from End of Therapy to Follow up.
The change in prevalence of double depression
Moods & Feelings Questionnaire (MFQ)
over the 3 time points in the Family Therapy group
There was a significant difference in the mean MFQ
was also statistically significant (v2 = 14.389; df = 2;
scores for both therapy groups at the different time
P = 0.001). The 2 · 2 v2 performed as above found
points, with the scores going down for both types of
that there was a statistically significant change in
therapy (see Table P < 0.001, power > 99%). There
prevalence of double depression from Baseline to End
was a slightly significant difference between the
of Therapy (v2 = 7.633; df = 1; P < 0.01), from
Individual Therapy and Family therapy groups by
Baseline to Follow up (v2 = 11.236; df = 1; P < 0.005)
Follow up (P < 0.05) but at low power (52%). There
but not from End of Therapy to Follow up.
was also a slightly significant difference between the 2
The prevalence of double depression in the Indi-
therapy groups over time (P < 0.05).
vidual Therapy group compared to the Family Ther-
In the Individual Therapy group, the mean drop in
apy group at End of Therapy was not statistically
MFQ score from Baseline to End of Therapy was 6.21,
significant, and this remained the case at Follow up.
with a further drop of 2.34 from End of Therapy toFollow up. (Total drop: 8.55) In the Family Therapy
j Additional measures of depression:
group, the mean drop in MFQ score from Baseline toEnd of Therapy was 9.95, but with only a further mean
Childhood Depression Inventory (CDI)
drop of 1.19 from End of Therapy to Follow up. (Totaldrop: 11.14)
There was a significant difference in the mean CDIscores for both therapy groups at the different timepoints, with the scores going down for both types of
j Measure of impairment/level of functioning
therapy (see Table , P < 0.001, power > 99%). Therewas no significant difference between the Individual
Children's Global Assessment Scale (C-GAS)
Therapy and Family therapy groups by Follow up.
There was a slightly significant difference between the
There was a significant difference in the mean C-GAS
2 therapy groups over time (P < 0.05, power < 80%).
scores for both therapy groups at the different time
European Child & Adolescent Psychiatry (2007) Vol. 16, No. 3 Steinkopff Verlag 2007
Table 4 Cases with one or more co-morbid conditions at three time points, by therapy type, based on the Kiddie-SADS
Individual therapy N = 35 (%)
Family therapy N = 37 (%)
Double depression
No double depression
Double depression
No double depression
Double depression
No double depression
a including imputed data for 4 ‘‘lost to follow-up'' cases
points, with the scores increasing for both types of
6 months following therapy. In addition, all remain-
therapy (see Table , P < 0.001, power > 99%). There
ing cases of depression (MDD, Dysthymia, and
was no significant difference between the Individual
‘‘double depression'') had resolved at the follow-up
Therapy and Family therapy groups by Follow up.
point. This suggests an ongoing response to therapy
There was also no significant difference between the 2
following completion, the sleeper effect.
therapy groups over time, specifically at End of
In the Family Therapy group, 75.7% of cases were
no longer clinically depressed following therapy, and
In the Individual Therapy group, the mean rise in
81% of cases were no longer clinically depressed
C-GAS score from Baseline to End of Therapy was
6 months later. Family therapy also appears to have
16.13, with a further rise of 3.84 from End of Therapy
been effective in cases of Major Depressive Disorder,
to Follow up (Total rise: 19.97). In the Family Therapy
Dysthymia and ‘‘double depression''. This effective-
group, the mean rise in C-GAS score from Baseline to
ness appears to have been persistent, with no relapses
End of Therapy was 17.05, with a further rise of 2.03
6 months following therapy. In addition, further
from End of Therapy to Follow up (Total rise: 19.08).
improvement in some of the remaining cases of
Secondary analysis using ML WIN confirmed the
depression (MDD, Dysthymia and ‘‘double depres-
above findings.
sion'') was found at the follow-up point, particularlyin cases of Dysthymia and ‘‘double depression''.
Response rates for depression in the Individual
Therapy and Family Therapy groups were not sig-nificantly different by End of Therapy. While re-
The presence of co-morbid conditions was assessed
sponse rates appear to have been approximately 20%
using the Kiddie-SADS (based on DSM IV criteria).
greater in the Individual Therapy group, compared to
The change in prevalence of cases with co-mor-
the Family Therapy group, at Follow up, this is very
bidity over the 3 time points in the Individual Ther-
largely influenced by the inclusion of the four ‘‘lost to
apy group, as depicted in Table was statistically
follow up'' cases in the Family Therapy group, who
significant (v2 = 19.821; df = 2; P < 0.001). The
were considered as unsuccessfully treated cases fol-
change in prevalence of cases with co-morbidity over
lowing therapy. Without these four cases, the differ-
the 3 time points in the Family Therapy group was not
ences in response rates between the two groups are
statistically significant, because of the absence of any
not statistically significant.
decrease from End of Therapy to Follow up. The
In addition to improvement as measured by cases
prevalence of cases with co-morbidity in the Indi-
no longer meeting diagnostic criteria for Major
vidual Therapy group compared to the Family Ther-
Depressive Disorder or Dysthymia, similar improve-
apy group at each of the three time points, however,
ment was found in both treatment groups in terms of
was not statistically significant.
level of impairment and level of functioning.
While final outcome appears to have been similar
in the two groups in many respects, the results from
the CDI and MFQ suggest a different pattern of re-sponse or improvement. With regard to the MFQ, the
In this study the following was found:
Family Therapy group had a lower score at End of
In the Individual Therapy group, 74.3% of cases
Therapy, despite having had a higher score than
were no longer clinically depressed following therapy,
the Individual Therapy group at Baseline. While the
and 100% of cases were no longer clinically depressed
power of this test was low (<80%), it does reflect the
6 months later. Individual therapy appears to have
slightly different ‘‘path'' for each of the therapy
been effective in cases of Major Depressive Disorder,
Dysthymia and ‘‘double depression''. This effective-
The Family Therapy group appears to have made
ness appears to have been persistent, with no relapses
greater improvement, in some respects, by End of
J. Trowell et al.
Childhood depression: a place for psychotheraphy
Therapy, compared to the Individual Therapy group.
therapy or supportive therapy with regard to rates of
These differences, though, had disappeared by Follow
remission, recovery, recurrence or level of function-
ing. In that study, the median onset of recurrence was
By Follow up, many of the Family Therapy trajec-
4 months after recovery, whereas in this study, there
tories appear to have plateaued, while the Individual
had been no recurrences, and ongoing improvement,
Therapy group trajectories suggest the possibility of
6 months post psychotherapy. Further research will
further, and possibly more rapid, improvement to
explore which components of the therapy were sig-
The population groups in the three countries ap-
pear to have responded similarly to the treatment.
Although not presented here, virtually no significantdifferences were found when similar analysis was
done comparing the three treatment centres (London,Athens, Helsinki), in terms of response rates and
Analysis has shown that both Focused Individual
Psychodynamic Psychotherapy (with Parent support
A significant number of cases in both therapy
work) and Systems Integrative Family Therapy were
groups had co-morbid conditions. Almost a third of
both effective in treating moderate to severe depres-
cases in the study had 3 or more co-morbid condi-
sion in children and young adolescents in three
tions. Following therapy, there was a decrease in co-
morbid conditions, particularly anxiety disorders and
This includes cases of dysthymia and ‘‘double
conduct disorders, which are often associated with
depression'' which are generally considered to be
depressive disorders. This occurred in both therapy
more difficult to treat. There has also been an overall
reduction in co-morbid conditions across the study.
The results of this study suggest both Individual
Therapy (response rate 74% by End of Therapy) andFamily therapy (response rate 75% by End of Ther-
Clinical implications
apy) may be more effective in the treatment ofdepression than other forms of treatment. Previousstudies have found a response rate in the region of
1. This study provides evidence supporting the use of
60% to CBT [] and 52–56% to Fluoxetine [
both Individual Psychodynamic Therapy and
and 71% to CBT and Fluoxetine combined [A
Family Therapy in this age group.
NNT analysis was undertaken using the End of
2. It may be possible for trained therapists, with the
Therapy results in this study. Using the Placebo data
help of the manuals, to deliver effectively, these
in the TADS study as a comparator, the NNT for both
focused forms of therapy.
Individual Therapy and Family Therapy is 3. This
3. Both treatments also appear to be exportable to
compares favourably with the NNTs reported in the
wider settings in culturally diverse populations.
TADS study, where the NNT for Fluoxetine and CBTcombined was 3, Fluoxetine was 4 and CBT was 12. Inthe absence of a control group in our study, a NNTanalysis was also conducted using the Nondirective
supportive therapy (NST) group from the Brent studyas an alternative comparator. The NNT for both
1. The study is limited by the sample size, which was
Individual therapy and Family therapy was 6. It is
influenced by recruitment difficulties. This be-
important to note in both the Individual and Family
comes even more significant when comparing
therapy groups, further improvement was reported at
smaller sub-groups e.g. countries, and therapy
Follow up. We would therefore expect to find lower
groups within countries.
NNTs at the Follow up point, were comparable data
2. The effect of the 4 ‘‘lost to follow up'' cases is also
significant, especially in relation to the total sample
The chronicity and severity of the depression in
size, and more so, because all of them were in the
our study led us to believe that spontaneous remis-
Family Therapy group. Intention to treat analysis
sion was unlikely to have occurred in the vast
principles were used in order not to lessen the
majority of cases, particularly in light of the extent of
power of the study or over-rate the effect of the
co-existing dysthymia. Furthermore, the TADS study
demonstrated a response rate of only 35% to placebo.
3. The absence of an ‘‘untreated'' control group limits
The Brent/Birmaher study , ] found that CBT did
the study's ability to prove with certainty the effi-
not confer any long-term advantage over family
cacy of the therapies provided.
European Child & Adolescent Psychiatry (2007) Vol. 16, No. 3 Steinkopff Verlag 2007
Jane Cassidy, Lois Colling, Carol Desousa (statistician), EmiliaDowling, Elspeth Earle, Anna Fitzgerald, Henia Goldberg, IngeGregorious, Agathe Gretton, Judith Loose, Ryan Lowe, Sue McNab,
Further analysis will be looking at whether differential
Gillian Miles, Renos Papadopoulos, David Pentacost, Maria Rhode,
predictors of response can be identified in the two
Margaret Rustin.
therapy groups, and whether there are any significant
Members of the Athens project team: Alexandra Alexopoulou, Evi
differences across the three different cultural settings.
Athanassiadou, Maria Belivanaki, Vaso Chantzara, Stelios Chris-togiorgos, Kostas Francis, Dimitris Georgiadis, Georgios Gritzelas,
Data from additional instruments about the child, his/
Terpsi Korpa, Olga Lanara, Effie Lignos, Dimitris Magriplis, Maria
her parents and family, and his/her environment will
Marangidi, Olga Maratos, Vasso Moula, Valeria Pomini, Eleni
provide further insight into the current findings. It
Stavrou, Marianna Tassi, Irene Tsanira, L. Tsarouhi.
will also be important to establish if any specific
Members of the Helsinki project team: Christina Bostrom, Taru
components of the respective forms of therapy were
Forst, Reija Graeffe, Susanne Friman, Kaarina Hastbacka, LiisaHisinger, Eija Korpinen, Anna Kuikka, Sakari Lehtonen, Helena
likely to have contributed to the patients' response.
Lounavaara-Rintala, Kaija Mankinen, Pirkko Pingoud, Liisa Pi-
Further studies should take measures to counteract
rhonen, Marja Schulman, Esko Varilo, Leena Varilo, Maija von
the limitations as discussed above. Other factors to
Fieandt, Pirjo Vuornos, Jan-Christer Wahlbeck, Hanna Westerinen.
consider would include gender distribution and
We would also like to thank the young people and their families fortheir contribution to the study.
family mental health history, as well as user prefer-
This study was partly funded by the European Community: Con-
ence for therapy type.
certed action contract No. BMH4-CT98-3231 DG12-SSMI. Centralco-ordination of the project took place at the Tavistock Clinic,London. Prof Kolvin was funded whilst developing the project by
j Acknowledgements Members of the London project team: Anne
the Leverhulme Foundation.
Alvarez, Sarah Barratt, Vicky Bianco, Susan Bliss, David Campbell,
1. Angold A, Costello EJ, Pickles A, et al.
7. Byng-Hall J, Campbell DC (1981)
12. Elkin I, Shea MT, Watkins JT, et al.
(1987) The development of a ques-
Resolving conflicts in distance regula-
(1989) National Institute of Mental
tionnaire for use in epidemiological
tion: an integrative approach. J Marital
Health treatment of depression collab-
studies of depression in children and
Fam Ther 7:321–330
adolescents. Institute of Psychiatry,
8. Committee on Safety of Medicines
effectiveness of treatment. Arch Gen
London University, London
(CSM) (2003) Selective Serotonin Re-
Psychiatry 46:971–983
2. Asarnow JR, Tompson M, Hamilton
uptake Inhibitors (SSRIs): overview of
13. Emslie GJ, Rush AJ, Weinberg WA, et
EB, et al. (1994) Family-expressed
regulatory status and CSM advice relat-
al. (1997) A double-blind, randomised
emotion, childhood-onset depression,
ing to major depressive disorder (MDD)
placebo-controlled trial of fluoxetine in
in children and adolescents including a
children and adolescents with depres-
spectrum disorders: is expressed emo-
summary of available safety and effi-
sion. Arch Gen Psychiatry 54:1031–
tion a non-specific correlate of child
cacy data: http://medicines.mhra.gov.
psychopathology or a specific risk fac-
14. Emslie GJ, Heiligenstein JH, Hoog S, et
tor for depression? J Abnorm Child
al. (2000) Fluoxetine for acute treat-
Psychol 22:129–146
9. Chambers W, Puig-Antich J, Hirsch M,
ment of depression in children and
3. Begg C, Cho M, Eastwood S, et al.
et al. (1985) The assessment of affective
disorders in children and adolescents
randomised clinical trial. Paper pre-
reporting of Randomised Controlled
by semi-structured interview: test–ret-
sented at 39th Annual Meeting of the
est reliability of the Schedule for
American College of Neuropsycho-
JAMA 276:637–639
Affective Disorders and Schizophrenia
pharmacology, December 10–14, 2000,
4. Birmaher B, Brent D, Kolko D, et al.
for school-age children, present epi-
San Juan, Puerto Rico
(2000) Clinical outcome after short-
sode version. Arch Gen Psychiatry
15. Garvin V, Leber D, Kalter N (1991)
term psychotherapy for adolescents
Children of divorce: predictors of
with major depressive disorder. Arch
10. Davenloo H (1978) Basic principles and
change following preventive interven-
Gen Psychiatry 57(1):29–36
techniques in short term dynamic
tion. Am J Orthopsychiatry 61(3):438–
5. Brent DA, Holder D, Kolko D, et al.
psychotherapy. Spectrum Publications,
(1997) A clinical psychotherapy trial
16. Goodyer IM, Herbert J, Secher SM, et
for adolescent depression comparing
11. Diamond G, Serrano A, Dickey M, et al.
al. (1997) Short-term outcome of major
cognitive, family, and supportive ther-
(1995) Current status of family-based
depression: I. Comorbidity and severity
apy. Arch Gen Psychiatry 54:877–885
outcome and process research. J Am
at presentation as predictors of persis-
6. Byng-Hall J (1995) Re-writing family
Acad Child Adolesc Psychiatry 35(1):6–
tent disorder. J Am Acad Child Adolesc
scripts: improvisation and systems
Psychiatry 36:179–187
change. Guilford Press, New York &
17. Harrington R, Dubicka B (2002) Ado-
lescent depression: an evidence-basedapproach to intervention. Curr OpinPsychiatry 15:369–375
J. Trowell et al.
Childhood depression: a place for psychotheraphy
18. Harrington R, Whittaker J, Shoebridge
25. Kolvin I, Trowell J, Tsiantis J et al
31. Parloff MB (1986) Placebo controls in
P (1998a) Psychological treatment of
(1999) Psychotherapy for childhood
psychotherapy research: a sine qua non
depression in children and adolescents.
depression. In: Maj M, Sartorius N
or a placebo for research problems. J
A review of treatment research. Br J
(eds) Evidence and experience in psy-
Consult Clin Psychol 54:79–87
chiatry, WPA Series, vol 1. John Wiley
32. Shaffer D, Gould MS, Brasic J (1993) A
19. Harrington R, Whittaker J, Shoebridge
children's global assessment scale (C
P, et al. (1998b) Systematic review of
26. Kovacs M (1981) Rating scales to assess
GAS). Arch Gen Psychiatry 40:1228–
efficacy of cognitive behaviour thera-
depression in school aged children.
pies in childhood and adolescent
Acta Paedopsychiatr 46:305–315
33. Tsiantis J, Kolvin I, Anastasopoulos D,
27. Kovacs M, Bastiaens LJ (1995) The
et al. (2005) Psychotherapy for early
adolescent depression (PEAD): a com-
20. Harter S (1990) Causes, correlates and
major depressive and dysthymic dis-
the functional role of global self-worth:
orders in childhood and adolescence,
interventions in three European coun-
a life-span perspective. In: Sternberg
issues and prospects. In: Goodyer IM
tries. In: Hibbs ED, Jensen P (eds)
RJ, Kolligian J (eds) Competence con-
(ed) The depressed child and adoles-
Psychosocial treatments for child and
sidered. Yale University Press, New
adolescent disorders: empirically based
Haven, pp 67–97
strategies for clinical practice. Ameri-
21. Kazdin AE (1986) Comparative out-
28. Malan DH, Osimo F (1992) Psychody-
can Psychological Association, Wash-
come studies of psychotherapy: meth-
namics, training and outcome in brief
ington, DC, pp 267–293
odological issues and strategies. J
psychotherapy. Butterworth, London
34. Will D, Wrate RM (1985) Integrated
Consult Clin Psychol 54:95–105
29. March J, Silva S, Petrycki JC, et al.
Family Therapy. Tavistock Publica-
22. Kolvin I, Garside RE, Nicol AR, et al.
(2004) Fluoxetine, Cognitive-Behavio-
(1981/5) Help starts here: the malad-
ural Therapy, and their combination
35. Wood A, Harrington R, Moore A
justed child in the ordinary school
(1996) Controlled trial of brief cogni-
Tavistock Publications, London
tive behavioural intervention in ado-
23. Kolvin I, MacMillan A, Nicol AR, et al.
Depression Study (TADS) Randomised
(1988) Psychotherapy is effective. J R
Controlled Trial. J Am Med Assoc
disorders. J Clin Psychol Psychiatry
Soc Med 261–266
24. Kolvin I, Barrett L, Bhate SR, et al.
30. Muratori F, Picchi L, Bruni G, et al.
(1991) The Newcastle child depression
(2003) A two-year follow-up of psy-
project: diagnosis and classification of
chodynamic psychotherapy for inter-
depression. Br J Psychiatry 159(11):9–
nalising disorders in children. J Am
Acad Child Adolesc Psychiatry 42(3):331–339
Source: http://www.vvpt.be/download/i/mark_dl/u/4012215687/4603890715/trowell-2007.pdf
Functional Foods in Health and Disease 2012, 2(3):48-61 Page 48 of 61 Research Article Open Access Anti-ulcer activity of Ipomoea batatas tubers (sweet potato) Vandana Panda*and Madhav Sonkamble Department of Pharmacology & Toxicology, Prin. K. M. Kundnani College of Pharmacy, Jote Joy Building, Rambhau Salgaonkar Marg , Cuffe Parade, Colaba, Mumbai 400005, India *Corresponding author: Vandana Sanjeev Panda, PhD, Prin. K. M. Kundnani College of Pharmacy, Colaba, Mumbai 400005, India Submission date: December 30, 2011, Acceptance date: April 31, 2012; Publication date: April 31, 2012 Abstract Background: Peptic ulcers occur in that part of the gastrointestinal tract which is exposed to gastric acid and pepsin, i.e., the stomach and duodenum. Gastric and duodenal ulcers are common pathologies that may be induced by a variety of factors such as stress, smoking and noxious agents including non-steroidal anti-inflammatory drugs. Ipomoea batatas tubers (sweet potato) contain ample amounts of antioxidants. It has been proven already by many scientific studies that antioxidants have ulcer healing properties. In reference to this, we tried assessing the ulcer healing effect of Ipomoea batatas tubers. Methods: The anti-ulcer activity of the tubers of Ipomoea batatas (sweet potato) was studied in cold stress and aspirin-induced gastric ulcers in Wistar rats. Methanolic extracts of Ipomoea batatas tubers (TE) at two doses, viz., 400 and 800 mg /kg were evaluated in cold stress and aspirin-induced gastric ulcer models using cimetidine and omeprazole respectively as standards. The standard drugs and the test drugs were administered orally for 7 days in the cold stress model and for 1 day in the aspirin-induced gastric ulcer model. Gastroprotective potential, status of the antioxidant enzymes {superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) and glutathione reductase(GR)} along with GSH, and lipid peroxidation were studied in both models. Results: The results of the present study showed that TE possessed gastroprotective activity as evidenced by its significant inhibition of mean ulcer score and ulcer index and a marked increase in GSH, SOD, CAT, GPx, and GR levels and reduction in lipid peroxidation in a dose dependant manner. Conclusion: The present experimental findings suggest that tubers of Ipomoea batatas may be useful for treating peptic ulcers. Key Words: Sweet potato tubers, cold stress, aspirin, ulcer, antioxidants.
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