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Method
Participants
Data were collected from 175 Pakistani Muslim patients
(105 males and 70 females) diagnosed as suffering from severe
psychotic depression. Participants were between 22 and 50 years
of age (mean age = 32.37 years, SD = 5.94) and were in-patients
at the Punjab Institute of Mental Health in Lahore. Participants
were matched for age and then assigned randomly to one of seven
groups as detailed below. Each group consisted of 25 patients
comprising 15 males and 10 females (consistent with the sex
distribution of patients).
Measures
Four measures were employed in the research. The Beck
Depression Inventory (BDI) consists of 21 groups of statements,
with each group consisting of four statements scored as 0, 1, 2, or
3 depending on their severity. The respondent selects the one
statement out of each group that best describes how they feel at
the present time. A total BDI score of 0-9 is considered normal,
scores of 10-16 are considered mild, scores of 17-29 are
considered moderate, and scores of 30-63 are considered
indicative of severe depression (Beck, Ward and Mendelson,
1961). The Hospital Anxiety Scale (HAS) and Hospital
Depression Scale (HDS) were developed to screen for clinically
significant anxiety and depression respectively in patients
attending medical clinics. Each scale comprises 7-item measures.
Each item has a 4-choice response format, scored as 0, 1, 2, or 3
depending on severity.
Patients are asked to tick the response that they feel seems
to be closest to what they have felt in the last few days. Their
score on the Hospital Anxiety Scale (HAS) and Hospital
Depression Scale (HDS) is then calculated. Scores higher than 10
are considered abnormal and the patient is diagnosed as suffering
from anxiety or depression (or both) respectively (Zigmond and
Snaith, 1983). Finally, doctors’ / psychologists’ / psychiatrists’
reports (DPPRs) were employed to gather information from the
medical duty officer under whose supervision the patient was
being treated: at the start of the study, information was collected
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Procedure
A randomized pre-test post-test group design was used.
The BDI HAS, and HDS were administered to all the participants
at the start of the study and DPPRs were also obtained. All the
participants were given similar doses of antidepressant drugs
(Fluoxetine and Amitryptiline) and antipsychotic drugs
(Haloperidol and Chloropromazine) daily, and they all attended
the same morning psychotherapy sessions thrice a week. Every
evening one hour of the participants’ time was employed for the
purposes of the study. During this time period, the patients of the
control group were free to pursue their own leisure interests (e.g.
watch TV, walk in the grounds etc.), whereas the patients of the
six experimental groups were taken to six different rooms, where
they were subjected to further treatment conditions. In each room,
a tape recorder was provided by the researcher and they were
asked to sit quietly and listen to the specific cassettes being
played in each room. Participants in each group listened to the
specific audio cassette assigned for their group for 60 minutes
daily over 30 days for six days a week. Sunday was a designated
family day that patients could spend entirely with their relatives.
Participants assigned to a ‘spoken religious’ group heard a
spoken lecture on the importance of the pillars of Islam.
Participants belonging to a ‘sung religious’ group heard the qirrat
EFFECT OF QURANIC RECITATION ON DEPRESSION 45
Table1
Mean Differences between the conditions
Change
in HAS 124.9 +.92 -4.00 - 9.52 +.44 -4.76 +.28 +.24
Change
in HDS 59.28 +.56 -.56 - 8.68 -.12 -4.96 -.12 4.0
Amount
of 11.03 - .76 - .96 - 3.40 -.92 -1.56 -.56 -.84
improvem
ent
(DPPR)
*p<0.001, df = 6 for each variable.
Key: CG, control group; EC1=Spoken religious words; EC2 = Sung religious
words; EC3 = Spoken uplifting words; EC4 = Sung uplifting words; EC5 = Spoken
Secular words; EC6 = Sung secular words
Table 2
Number of participants who improved
Any improvement
Group No Yes
Control group 18 7
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