Hosiana Fajar Wulan Jurnal
Hosiana Fajar Wulan Jurnal
DOI: 10.1111/ppc.12325
ORIGINAL ARTICLE
1
Postgraduate Program: Psychiatry and
Behavioral Science, Universidade Federal do Abstract
Rio Grande do Sul (UFRGS), Porto Alegre (RS), Purpose: Our aim was to evaluate the effects of deep breathing exercises in subjects
Brazil
2 with bipolar disorder.
Laboratory of Molecular Psychiatry, Hospital
de Clínicas de Porto Alegre (HCPA), Porto Design and Methods: This was an open‐label, uncontrolled clinical trial with three
Alegre, Brazil
assessments: preintervention, postintervention, and follow‐up.
Correspondence Findings: The Hamilton Anxiety Rating Scale, BECK‐A, Hamilton Depression Rating
Mauricio Kunz, Laboratory of Molecular
Scale, and Young Mania Rating Scale had significant preintervention, postinterven-
Psychiatry, Hospital de Clínicas de Porto
Alegre (HCPA), Ramiro Barcelos 2350, Porto tion, and follow‐up differences. The results indicated that the deep breathing protocol
Alegre, RS 90035003, Brazil.
was effective in reducing anxiety levels in patients with bipolar disorder. The deep
Email: [email protected]
breathing protocol has no negative side effects and might be applied to decrease
anxiety symptoms in individuals with bipolar disorder.
Practice implications: The results provide direction for providing quality care that
reduces anxiety levels in patients with bipolar disorder.
KEYWORDS
anxiety, bipolar disorder, deep breathing
Therefore, our goal was to verify if a deep breathing protocol is a of the scale, and the result ranges from 0 to 56.17,18 In anxiety
feasible and effective treatment of anxiety in patients with BD. studies, response to the treatment was defined as a ≥ 50% decrease
in HAM‐A, whereas the definition of remission was based on a
score less than or equal to 7 on HAM‐A.19 The BAI is a self‐reported
2 | METHODS
scale consisting of 21 questions, rated on a 4‐point Likert scale, which
referred to the experience of symptoms last week. Scores for the 21
2.1 | Participants
items are summed to produce a single anxiety index, ranging from 0
The Ethics and Research Committee of the Hospital de Clínicas de to 84 points.20 BAI has adequate test‐retest reliability and
Porto Alegre (HCPA) approved the study. Patients were 20 convergent validity.21
outpatients from the Bipolar Disorder Program and the Support
Group for Patients and relatives with BD at the HCPA. Inclusion
2.5 | Quality of life
criteria were patients who had a diagnosis of BD according to the
diagnostic and statistical manual of mental disorders (DSM-5), were The quality of life of each patient was evaluated with the Short‐Form
male or female, were between 18 and 69 years old, had euthymia for Health Survey (SF‐36) that comprises 36 questions and is subdivided
at least 1 month before the assessment confirmed by the Hamilton into eight domains: functional capacity, body pain, vitality, general
Depression Rating Scale (HAM‐D‐17) and Young Mania Rating Scale health, social function, physical and emotional function, and mental
(YMRS) less than or equal to 7, had a stable pharmacological health. The values range from 0 to 100, and larger numbers
treatment for at least 3 months, and had current complaints of represented a better health‐related quality of life.22
anxiety symptoms as evaluated by the attending physician. Patients
who met the inclusion criteria and who gave their written informed
2.6 | Functionality
consent were invited to the preintervention evaluation.
Patients who had obstructive and restrictive respiratory diseases, The Functional Assessment Short Test (FAST) was used to evaluate
patients diagnosed with a clinical contraindication, and patients the functionality of patients in the last 15 days. It consisted of 24
meeting the criteria for acute mania or depression and needed a items that are divided into six areas of functionality: autonomy, work,
modification in their current medication regimen were excluded from cognition, finance, interpersonal relationships, and leisure. The items
the study. were scored on a 4‐point scale, where 0 is no difficulty; 1, few
difficulties; 2, moderate difficulties; and 3, serious difficulties. The
higher the score was, the more serious the difficulties were.23
2.2 | Study design
This was an open‐label, uncontrolled clinical trial with three
2.7 | Biological rhythms
assessments: preintervention, postintervention, and follow‐up.
The biological rhythms of the patients were evaluated through the
Biological Rhythms Interview for Assessment in Neuropsychiatry
2.3 | Assessments
(BRIAN) scale. The BRIAN scale evaluated the regularity of biological
Three evaluations were performed. Initially, a clinical and socio- rhythms in four different domains: sleep, activities, social, and food.
demographic evaluation questionnaire was applied, usually by This scale consists of 21 items, 18 divided into three specific areas:
researchers at the Laboratory of Molecular Psychiatry of the HCPA, sleep/social, activity, and food. Total scores range from 18 to 72, and
and included the structured interview Mini International Neuropsy- higher scores indicated a greater disruption in the biological
chiatric Interview 5.0 for the diagnostic evaluation and scaling of rhythm.24
mood symptomatology (eg, the HAM‐D and the YMRS).
To verify breathing patterns, cirtometry was used, which
2.8 | Satisfaction of the patients with deep
consisted of a set of measurements of the circumferences of the
breathing
thorax and abdomen during respiratory movements and aimed to
quantify thoracoabdominal mobility.16 To evaluate the patient satisfaction with the deep breathing protocol,
the adapted Andrews Face Scale was used with scores varying from 0
to 10, with 0 being totally dissatisfied and 10 being totally satisfied.25
2.4 | Anxiety
Although there is no validation study for the Brazilian population,
The Hamilton Anxiety Rating Scale (HAM‐A) and the Beck Anxiety this scale has been widely used.
Inventory (BAI) were used to assess anxiety symptoms. The HAM‐A
comprises 14 items distributed in two groups: the first group of
2.9 | Physical activity
seven items is related to symptoms of anxious mood, and the second
group of seven items is related to physical symptoms of anxiety. The To evaluate the level of physical activity, the International Physical
total score is obtained by summing the assigned values in all 14 items Activity Questionnaire scale was used, which is an instrument to
SERAFIM ET AL. | 3
F I G U R E 1 Deep breathing protocol. BRIAN, Biological Rhythms Interview for Assessment in Neuropsychia try; FAST, Functional
Assessment Short Test; HAM‐D, Hamilton Depression Rating Scale; SF‐36, Short‐Form Health Survey; YMRS, Young Mania Rating Scale
estimate the level of habitual practice of activity. It is composed of performed. In the fifth session, patients performed the deep
eight open‐ended questions and estimates the time spent per week in breathing exercises and were also given written instructions on the
different aspects of physical activity (eg, moderate physical activity, deep breathing techniques for further practice at home. The patient
vigorous walking, and physical exertion) and physical inactivity was seen for the final follow‐up assessment and evaluation (Figure 1).
(sitting position). It classifies the patient into a number of categories,
including sedentary (patient does not perform any regular activity for
2.12 | Statistical analysis
10 continuous minutes) and irregularly active (one that performs
physical activity but at a level insufficient to be classified as active Statistical analyses were performed in R (https://www.Rproject.org/).
because it does not comply with the recommendations regarding Descriptive statistics were collected from clinical and demographic
frequency or duration). Irregularly active is divided into two data. The means (with standard deviation) and frequencies (numbers
subgroups: irregularly active B (someone who did not meet any of or percentages) were used to describe the characteristics of the
the criteria of the recommendations regarding frequency or duration) sample.
and irregularly active A (someone who meets at least one of the To test the effect of the intervention, the “easyanova” package
criteria of the recommendations regarding the frequency (5 days/ was used.29 The comparison of the preintervention, postintervention,
week) or duration (150 min/wk) of the activity. It also ranks people as and follow‐up evaluations was performed by analysis of variance of
active (ie, the patient fulfilled the recommendations of vigorous the following variables: HAM‐D, YMRS, FAST, HAM‐A, BAI,
activity ≥ 3 days/wk and ≥20 min/session, or moderate activity or SF‐36, and BRIAN. The Scott–Knott test was performed to compare
walking, ≥5 days/wk and ≥30 min/session or 5 days/wk and the means of the variables that presented significant differences in
≥150 min/week [walk + moderate + vigorous]) and very active (pa- ANOVA (P < 0.05). The breathing pattern, because it was a
tient met the recommendations of vigorous activity, ≥5 days/wk and categorical variable, was analyzed in an organizational tree model,
≥30 min/session, vigorous activity ≥ 3 days/wk ≥ 20 min/session + using the "rpart" package,30 and the significance of the intervention
moderate activity and/or walking ≥5 days/wk and ≥30 min/ was obtained by the chi‐square test with the package “stats” (native
session).26 R package). The χ2 test was applied when the dependent and
independent variables were categorical, by comparing the group
variances and between groups.31
2.10 | Estimated intellectual functioning (IQ)
The graphs for the presentation of the results were produced
Estimated IQ was assessed with two subtests from the Wechsler with the package "ggplot2".32
Abbreviated Scale of Intelligence: Vocabulary and Matrix Rea-
soning.27,28
3 | RESULTS
2.11 | Intervention
Twenty patients were asked to participate in the study and
The deep breathing protocol was performed at the Clinical Research completed the preintervention evaluation, but 14 patients completed
Center of Hospital de Clínicas de Porto Alegre. The protocol the protocol, as three of the patients dropped out of the study due to
comprised seven sessions that lasted between 30 and 60 minutes, logistical issues and three were excluded from the study because
and during these weekly, individualized sessions, the patient was they did not meet all the inclusion criteria. Of the 20 patients who
guided by the same physiotherapist throughout the protocol. In the performed the first evaluation, 14 patients (70%) were female. The
first session, the preintervention assessment was performed, and mean age was 42.80 (±12.06) years. Thirteen patients (65%) were
information about the deep breathing was shared. During the second sedentary, five patients (25%) were irregularly active A, and two
session, the patient was shown how to perform deep breathing. In patients (10%) were irregularly active B and so remained in the
the third and fourth sessions, the deep breathing training was subsequent assessments. The other data can be seen in Table 1.
4 | SERAFIM ET AL.
T A B L E 1 Demographic and clinical characteristics of participants The comparisons of preintervention, postintervention, and
Abbreviations: BRIAN, Biological Rhythms Interview for Assessment in Neuropsychia try; FAST, Functional Assessment Short Test; HAM‐D, Hamilton
Depression Rating Scale; SF‐36, Short‐Form Health Survey; YMRS, Young Mania Rating Scale.
a,b
Means followed by the superscript letters did not differ according to Scott–Knott test at 5% significance.
SERAFIM ET AL. | 5
F I G U R E 3 HAM‐A and BAI preintervention , postintervention, and follow‐up assessment. HAM‐A, Hamilton Anxiety Rating Scale; BAI, Beck
Anxiety Inventory
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