Siddiqui Shah Depression Scale SSDS Deve
Siddiqui Shah Depression Scale SSDS Deve
non-clinical samples respectively. The Alpha coefficients for the clinical and
non-clinical samples were 0.91 and 0.89 respectively. The scale correlated sig-
nificantly with Zung’s Depression Scale, r 0.55 (p < .001) and psychiatrists’ rat-
=
ings of depression r 0.40 (p < .05). The scale showed a significant correlation
=
with subjective mood ratings for the clinical group r 0.64 (p < . .001) as com-
=
pared to the non-clinical group r = 0.14 (p: n.s.). The scale also demonstrated
high sensitivity and specificity. The percentiles and cut-off scores for the clinical
as well as non-clinical groups have been determined.
Siddiqui-Shah Depression
Scale (SSDS): Development
and Validation
SALMA SIDDIQUI
Quaid-i-Azam University
Islamabad
Method
Phase I
Phase II
As the items for the scale were generated by the student sam-
ple,it was considered necessary to estimate the intensity of the
250/
denoted normal sadness, &dquo;2&dquo; mild depression, and &dquo;3&dquo; severe de-
pression. If an item appeared more characteristic of normal sad-
ness, it was rated as &dquo;1&dquo;, if it was found to be reported more
frequently by mildly depressed persons, the item was given a rat-
ing of &dquo;2&dquo;, and if the item was considered as characteristic of se-
verely depressed patients, it was rated as &dquo;3&dquo;. This helped
determine the classification of items as characteristic of normal
sadness, mild depression or severe depression. On the basis of
this pilot study, the items for the final scale were selected. Fre-
quencies and percentages were obtained forwach item, which in-
dicated the judges’ consensus for assigning items to one of the
three categories (see Table 1). Items which had above 50% con-
sensus among the judges were selected for the final scale. How-
ever, in the categories of normal sadness and &dquo;severe depression&dquo;
the criterion had to be lowered to 47% for a few items so as to
have an equal number of items in each category. In all, 36 items
were retained, 12 in each category, that is, normal sadness, mild
Phase III
Results
The data obtained in phase III of the study provided the differ-
ential analysis of the 36-item scale between the clinical and
non-clinical groups. The clinical group had a higher mean and
SD (mean: 51.93, SD: 18.33) than the non-clinical group (mean:
27.93, SD: 12.7).
Item Analysis
Split-half Reliability
As the items of the scales were randomly ordered (in terms of
the relevance of the items) into two equal halves, split-half reli-
Table 1
Item-total Score Correlation for Indigenous Depression Scale
Table 1 continued
/ 253
Table 1 continued
*
p < 0.05, ** p < 0.01.
Table 2
Correlation Coefficients for Split-half Reliability and Spearman-Brown
Correction of the Scale for Clinical and Non-clinical Groups
254 /
sistency of the scale. The value obtained for the clinical group
was 0.91 (p < .001) and for the non-clinical group 0.89 (p < .001).
Table 3
Internal Consistency of the Scale for Clinical and Non-clinical Groups
Construct Validity
The correlation between the scores of the non-clinical group
on the 36-item scale and Zung’s Depression Scale indicated a
value of r: 0.55 (p < .001). The scores of the clinical group were
significantly correlated with the psychiatrists’ ratings for depres-
sion (r: 0.4, p < .05). The scores of the clinical group on the scale
correlated significantly with their self-reported mood (r: -0.64, p
< .001), whereas the correlation of the scores of the non-clinical
group with their subjective mood ratings was not significant (r:
0.14, p>.05).
Table 4
Construct and Concurrent Validity of Indigenous Depression Scale
255
Factorial Validity
Table 5
Eigen Values and Percentage of Variance Explained by the
Extracted Factors
Cut-off Scores
As the scale measures the frequency of the indicators of depres-
sion, the subject’s score is determined by the category of en-
dorsement of his/her responses. The frequency distribution of
the computed for both the clinical and non-clinical
score was
Discriminant Validity
A discriminant index for each cut-off score (26, 37 and 50) was
obtained by dichotomising the frequencies of false positives and
’alse negatives around each cut-off score. This resulted in 3 2 x 2
:ontingency tables (Tables 6, 7 and 8). It can be seen from Table
/ 257
Table 6
Discriminant Validity of the Sccsle for tbe Cutting Score oJ below and
above, 26 for Depressed and Non-depressed Groups
Table 7
Discriminant Validity of tbe Scale for the Cutting Score of below and
above, 37 for Depressed and Non-depressed Groups
Table 8
’
Discriminant Validity of the Scale for the Cutting Score of, below and
above, 50 for Depressed and Non-depressed Groups
high discriminant validity for the cut-off score of 26 (phi: 0.42; chi
square: 46.9, df: 1, p < .0001).
It can be seen from Table 7 that below the cut-off score of 37,
the frequency of non-cases in the non-clinical sample was 173,
whereas 33 individuals in the non-clinical group were classified
as false positive at this cut-off point. In comparison, only 14 cases
in the clinical group were labelled as non-cases and 46 were
258 /
Further, Table 8 shows that below the cut-off score of 50, the
frequency of non-cases in the non-clinical sample was 193,
whereas 13 individuals in the non-clinical group were classified
as false positive at this cut-off point. In comparison, 30 cases of
the clinical group were labelled as non-cases and 30 were diag-
nosed as depressives at this cut-off score. The phi-coefficient
demonstrated a significantly high discriminant validity for the
cut-off score of 50 (phi: 0.48; chi square: 60.45, df: 1, p < .0001).
Discussion
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Syed Ashiq Ali Shah is Associate Professor of Psychology at the International Is-
lamic University, Selangor, Malaysia. His research interests are in the areas of
culture and psychopathology.