Skip to main content
PLOS One logoLink to PLOS One
. 2025 Jan 24;20(1):e0318062. doi: 10.1371/journal.pone.0318062

Validation of the somatic symptom disorder—B Criteria Scale (SSD-12) in Bangladesh

Sumaiya Habib 1, Muhammad Kamruzzaman Mozumder 1,*
Editor: Kenta Matsumura2
PMCID: PMC11760037  PMID: 39854595

Abstract

Background

The absence of a reliable and valid Bangla instrument for measuring somatic symptom disorder hinders research and clinical activities in Bangladesh. The present study aimed at translating and validating the Somatic Symptom Disorder-B criteria (SSD-12).

Method

A cross-sectional design was used with purposively selected clinical (n = 100) and non-clinical (n = 100) samples. The clinical sample was collected from psychiatric departments at three hospitals, while the non-clinical sample was drawn from the local community. Exploratory (EFA) and confirmatory factor analysis (CFA) were conducted on the SSD-12, along with reliability and validity assessments.

Results

Results indicated satisfactory internal consistency reliability (Cronbach’s alpha = .94, split-half r = .93); criterion-related validity (r = .86, with Morey’s Somatic Complaints Scale); and construct validity (r = .64 with anxiety subscale and r = .57 with depression subscale of the Hospital Anxiety and Depression Scale) of the translated scale. In contrast to the three-factor structure of the original SSD-12, the Bangla version indicated a single-factor structure (accounting for 61.29% of the total variance). This scale also demonstrates its ability to distinguish between clinical and non-clinical participants (t198 = 16.74, p < .01).

Conclusion

The Bangla translated SSD-12 has demonstrated strong psychometric properties, indicating its suitability for use in Bangladesh. This tool is expected to aid mental health practitioners in their clinical work by providing them with a quick assessment of their patients having somatic complaints.

Introduction

Patients at all stages of healthcare, frequently experience physical complaints such as pain in various body parts, exhaustion, or other problems with the bodily systems. The severity spectrum of these complaints and sufferings may range from minor signs with little functional impairments to diseases that are entirely incapacitating. However, a significant portion of these presentations are the result of a psychogenic process [1]. Psychiatric diagnoses such as Somatic Symptom Disorder (SSD) [DSM-5; 2] or Bodily Distress Disorder [ICD-11; 3] are often missed for these patients [1]. This misdiagnosis often contributes to lengthy and ultimately ineffective therapy resulting in a substantial increase in the cost of treatment, burden of disease, and distress in the treating physicians [4]. Early and accurate identification of the disorder is therefore crucial for somatic symptoms.

Somatization disorders are characterized by a lifetime history (generally beginning before age 30) of seeking treatment for or becoming impaired by multiple physical complaints that cannot be fully interpreted by medical causes and are not intentionally feigned [5]. Somatization is generally characterized by three distinct features [6]. Firstly, it presents with medically unexplained somatic symptoms such as pain, weakness, or shortness of breath. Secondly, patients exhibit somatic preoccupation or hypochondriacal worry demonstrating excessive engagement (in terms of time and effort), and concerns about their bodily symptoms. These concerns often are overtly disproportionate and may be accompanied by excessive body checking and reassurance-seeking [7]. Thirdly, patients may present these somatic symptoms as part of the clinical manifestations of anxiety, affective, or other psychiatric disorders [6].

Somatization may present with a range of symptoms, Bangladeshi children and adolescents diagnosed with somatoform disorder report an average of 12 to 16 somatic symptoms [8]. Pain is the most common symptom among patients. In Bangladesh, abdominal pain is the most frequent somatic symptom in children and adolescents [8], while a German study of 7,925 adults aged 40 to 80 years found that pain complaints (arms, legs, joints, back pain) were most common, followed by back pain, headaches, nausea, constipation/diarrhea, shortness of breath, dizziness, and heart racing or pounding [9].

Across the globe, including Bangladesh, somatic symptom disorders have been reported to be the third most prevalent mental disorder after anxiety disorders and depression [10, 11]. Mohit [12] found that 6.6% of the patients from the outpatient department at the specialized mental hospital suffer from somatoform disorder, while a recent nationwide survey revealed a prevalence of about 2.1% among the adult population (105 million) in Bangladesh [11].

Somatoform disorders are among the most common psychiatric disorders in general medical settings. Somatoform disorders often coexist with other comorbidities, with 8% of primary care patients meeting the criteria for ’multi-somatoform disorder’[13]. Depression, conversion disorder, hypochondriasis, somatization, and pain disorders are the most common comorbid conditions associated with somatization [14]. Apart from comorbidity, somatization disorder has been reported to be strongly associated with depression and anxiety, moderately with schizophrenia and mania, and weakly with substance use and antisocial personality [15]. Accurate diagnosis, support, and reassurance are the cornerstones of the treatment of somatization disorder [16]. Approaches typically involve psychotropic medications and psychological therapies (such as, cognitive behavior therapy) focusing on cognitive, emotional, and behavioral aspects [17]. The prognosis for somatic symptom disorder shows improvement in 50–75% of patients, while 10–30% experience a worsening of their condition under combination treatment (medication and psychological therapy) [18]. Fewer symptoms and higher baseline functioning have been linked with a better prognosis [19].

An accurate identification and assessment of somatic symptom disorders in a clinical setting is necessary for effective intervention. However, the assessment of SSD is challenging due to a variety of diagnostic difficulties including symptom overlap. Such overlap may be observed with medical conditions [20] and with other mental illnesses such as illness anxiety disorder, conversion disorder, psychological factors affecting medical conditions, and factitious disorder [21]. Numerous questionnaires such as the somatization subscale of the Symptom Checklist-90 [22] and the Patient Health Questionnaire (PHQ-15) [23] are available for assessing somatic symptoms in the general population. However, none of them are suitable for diagnostic purposes as they fail to capture psychological attributes.

In clinical settings, the Structured Clinical Interview for DSM-5 [SCID-5; 24] is considered the gold standard for diagnosing DSM-5 disorders. However, as a time-consuming process, conducting SCID is often not feasible, especially in resource-constrained settings such as Bangladesh. Although the recently available Bangla tool "Morey’s Somatic Complaints Scale (SCS)" [25] is utilized for assessing somatic complaints as part of a larger Personality Assessment Inventory (PAI), it is not designed or suitable for diagnosing or assessing criterion B of somatic symptom disorder. The Somatic Symptom Disorder–B Criteria Scale [SSD-12; 20] is a brief self-report tool specifically designed to evaluate DSM-5 criterion B of the somatic symptom disorder and hence is suitable for diagnosing the disorder. The SSD-12 assesses patients’ cognitive, affective, and behavioral symptoms and therefore, has additional clinical utility along with diagnostic use. Translation and validation of the SSD-12 scale in Bangla seemed prospective for its clinical as well as research application with SSD patients. It is expected that the Bangla version of the instrument will assist in prompt diagnoses leading to early and accurate intervention, which will enhance the quality of life of the patients.

Methods

Participants

This study employed a cross-sectional design. Purposive sampling was used to recruit 200 participants (100 clinical, 100 non-clinical). The clinical sample was collected from the psychiatric departments of three hospitals while the non-clinical sample was collected from the general population from the local community. The clinical participants, diagnosed by psychiatrists, met DSM-5 diagnostic criteria for somatic symptom disorder, while the non-clinical participants had no history of any psychiatric disorders. The inclusion criteria required the participants to be adults (i.e., age above 18 years) and to meet the group criteria (diagnosis of somatic symptom disorder for the clinical group and no mental illness for the non-clinical group). The exclusion criteria included the presence of active suicide risk (< 3 months), intoxication with substance, intellectual disability, and inability to communicate in Bangla. Demographics revealed the predominance of females (63%) over males (37%) in the total sample who had an age range of 18 to 65 years (M = 30.02, SD = 8.99). Among the participants, 17% completed primary education, 39% held bachelor’s degrees, and 26% held master’s degrees or equivalent. The majority (66.5%) of them described their economic condition as average, while 21% described it as below average. Data for this study were collected from the psychiatric departments of three tertiary hospitals, providing access to a diverse patient population. For one of the hospitals, the majority of the data were collected from the inpatient department, while for another, the majority came from the outpatient department. These differences may result in inadvertent variation in the patient groups across the three settings. However, as no comparisons between the settings were planned, we believe these variations rather contributed to the generalizability of the findings.

Instruments

A custom-built socio-demographic information questionnaire was used to collect information about the participants’ age, sex, education, marital status, and socio-economic status. Additionally, three established scales were used to measure different constructs as part of the validation process of the SSD-12. Participants were instructed to complete the SSD-12 questionnaire based on their experiences over the last one week, aiming to capture the severity of recent symptoms and their impact.

Somatic Symptom Disorder–B Criteria Scale [SSD-12; 20]. The SSD-12 consists of 12 items distributed over cognitive, affective, and behavioral domains that reflect in a three-factor structure [20]. The respondents report their experiences of cognition, emotion, or behavior on a 5-point Likert scale such as, “I think that my physical symptoms are signs of a serious illness”, “I am very worried about my health”, “My health concerns hinder me in everyday life”. The total score ranged from 0 to 48 with higher scores indicating higher severity of SSD. Adequate reliability (Cronbach’s alpha = .95) of the SSD-12 has been reported, along with a high correlation between somatic symptoms (r = .47, p < .01), depressive symptoms (r = .22, p < .01), and health anxiety (r = .71, p < .01), confirming the validity of the test [20].

Morey’s Somatic Complaints Scale [SCS; 26]. The SCS has three subscales assessing conversion, somatization, and hypochondriasis [26]. The somatization subscale of the Bangla SCS [25] was used as the criterion measure in evaluating the construct validity of the SSD-12. Satisfactory psychometric properties where construct validity at r = .925, (with GHQ-28) and Cronbach alpha at .97 of the Bangla SCS have been reported [25].

Hospital Anxiety & Depression Scale [HADS; 27]. The HADS [27] is a widely recognized and commonly used self-report instrument that measures depression and anxiety as two distinct dimensions, each with 7 items, using a 4-point response scale ranging from 0 (no distress) to 3 (significant distress). This scale was found to perform well in assessing the severity of anxiety and depression in both somatic and psychiatric cases and the general population [28]. It was hypothesized that individuals with higher somatic complaints would have a higher level of anxiety and depression [29] and hence, the HADS was used to assess criterion validity of the Bangla SSD-12.

Procedures

Translation and back-translation were done following the International Test Commission’s guidelines [30] in preparing the Bangla version of the SSD-12 scale. Two bilingual experts translated the questionnaire from English to Bangla, and their translations were synthesized into one version, which was then back-translated into English by another bilingual expert. The back-translation was compared with the original English version by the original author of SSD-12, and no discrepancies in the meaning of any items were reported. Details on the processes used in the translation and validation of the SSD-12 are presented in Fig 1.

Fig 1. Flow chart of the process involved in the translation and validation of SSD-12.

Fig 1

Data were collected during COVID-19 pandemic restrictions, where lockdowns and fears prohibited many patients from accessing mental health care. This resulted in a smaller sample size and elongated the data collection period (October 2021 to March 2023). Before data collection, researchers explained the study’s objectives, potential risks and benefits, and participants’ right to withdraw. All the participants provided written informed consent. The project received ethical approval prior to data collection from the Ethics Committee of the Department of Clinical Psychology, University of Dhaka (protocol# MS210504, approved on 18 May 2021).

Findings

Validity

The content in the items of the Bangla SSD-12 went through rigorous evaluation during forward and backward translation. As no changes other than translation were made to the original English version with known content validity [20], the Bangla SSD-12 can be claimed to have content validity.

The criterion validity of the Bangla SSD-12 was evaluated using its correlation with the Somatic Complain Subscale (SCS) of the Morey Personality Inventory [25, 26]. The SCS was considered as the criterion measure and a high correlation r = .86 (p < .01) was found between scores of the Bengali SSD-12 and the SCS (Table 1).

Table 1. SSD-12 correlations with SCS, HADS, and its anxiety and depression subscales.

Type of Validity Instruments Coefficient Cohen’s d
Criterion Somatic complain scale (SCS) r = .86** 3.34
Criterion Somatization diagnosis t198 = 16.74** 2.37
Construct (Convergent) Psychological distress (HADS) r = .67** 1.79
Construct (Convergent) Anxiety subscale of HADS r = .64** 1.65
Construct (Convergent) Depression subscale of HADS r = .57** 1.37

**p < .01.

Diagnostic status was used as an additional criterion for assessing criterion validity of the Bangla SSD-12 so independent samples t-test was used to compare the mean SSD-12 scores of clinical and non-clinical samples. Significant difference (t198 = 16.74, p < .01) between scores for clinical (M = 31.61, SD = 7.60) and non-clinical (M = 11.81, SD = 9.06) groups was found. Additionally, to assess the diagnostic accuracy of the SSD-12, the Receiver Operating Characteristic (ROC) curve was used (Fig 2).

Fig 2. Receiver Operating Characteristic (ROC) curve for SSD-12.

Fig 2

The area under the curve was .936 (95% CI [.903, .969], p < .01), indicating excellent diagnostic performance. The sensitivity-specificity calculation suggests the optimal cutoff score of 22 with a sensitivity of 0.89 and a specificity of 0.84 (Table 2).

Table 2. Sensitivity and specificity of the SSD-12 in the intermediate range.

Score Sensitivity Specificity
13.50 1.00 .710
19.50 .910 .790
20.50 .910 .810
22.00 * .890 .840
23.50 .830 .850
24.50 .830 .890
37.50 .260 .010

* Optimal cutoff score

The convergent method was used to assess construct validity of the Bangla SSD-12. As somatic problems are known to increase the psychological burden of a person [20], it was hypothesized that people with higher somatic complaints would have higher levels of psychological distress, anxiety and depression compared to those without such complaints [31]. Similar to previous studies, the HADS was used to assess construct validity in this regard [27]. The SSD-12 total score was found to have adequate positive correlations with the overall HADS score (r = .67, p < .01), its anxiety subscale (r = .64, p < .01), and its depression subscale (r = .57, p < .01) (Table 1).

Reliability

Internal consistency reliability of the SSD-12 was tested through three indicators; corrected item-total correlation, Cronbach’s alpha and split-half correlation. The corrected item-total correlation demonstrated adequate correlation of the individual items with the corrected total scores (average r = .731; range r = .463 to .817) (see Table 3). The overall Cronbach’s alpha for the 12-item scale was .94, indicating high internal consistency of the translated instrument (Table 3). Additional support for the internal consistency of the instruments came from split-half reliability which was calculated using the odd-even method and demonstrated a strong correlation (Spearman-Brown r = .93).

Table 3. Itemized statistics for internal consistency and factor analysis.

Items Corrected item-total correlation Factor loading
1 I think that my physical symptoms are signs of a serious illness .728 .775
2 I am very worried about my health .638 .695
3 My health concerns hinder me in everyday life .761 .807
4 I am convinced that my symptoms are serious .790 .832
5 My symptoms scare me .810 .849
6 My physical complaints occupy me for most of the day .783 .824
7 Others tell me that my physical problems are not serious .463 .517
8 I’m worried that my physical complaints will never stop .788 .833
9 My worries about my health take my energy .798 .839
10 I think that doctors do not take my physical complaints seriously .613 .671
11 I am worried that my physical symptoms will continue into the future .783 .825
12 Due to my physical complaints, I have poor concentration on other things .817 .856

Factor analysis

Confirmatory Factor Analysis (CFA)

As the original scale has been known to have a three-factor structure [20], we conducted a confirmatory factor analysis to assess the fit of the known factor structure with Bangladeshi data. The three-factor measurement model (see Fig 3) was tested using AMOS 18 software program [32]. Several fit indices were consulted to assess the adequacy of the three-factor model, including Chi-square (χ2), the ratio of Chi-square to degrees of freedom (χ2/df), root mean square error of approximation (RMSEA), comparative fit index (CFI), Tucker-Lewis index (TLI), and standardized root mean square residual (SRMR). The criteria for evaluating goodness of fit were as follows: χ2 with p ≥ .01, χ2/df ≤ 2, RMSEA ≤ .06, CFI ≥ .95, TLI ≥ .95, and SRMR ≤ .08 [see 33]. None of the indices suggested fit of the three-factor model (χ2 = 245.11, p < .01; χ2/df = 4.81; RMSEA = .138; CFI = .895; TLI = .864, and SRMR = .058) for the Bangla SSD-12 (Table 4). Subsequently, an exploratory factor analysis was carried out to identify the factor structure of the Bangla SSD-12.

Fig 3. Fitness of the measurement model showing loadings on two alternative factor structures.

Fig 3

Table 4. The goodness of fit indices for three-factor and one-factor model of SSD-12 measurement structure.
χ2 df p χ2/df RMSEA [CI] CFI TLI SRMR
Three-factor model 245.11 51 .01 4.81 .138 [.121, .156] .895 .864 .058
One-factor model 317.97 54 .01 5.89 .157 [.140, .174] .857 .825 .055

Exploratory Factor Analysis (EFA)

The Kaiser-Meyer-Olkin value (.91) and Bartlett’s test of sphericity (χ2 = 1864.32, p < .01) indicated sampling adequacy and suitability of the data for factor analysis [34, 35]. The Eigenvalues and scree plot (Fig 4) suggested one factor, accounting for 61.29% of the total variance. All the items displayed adequate factor loadings for their retention under the single factor (see Table 3).

Fig 4. Scree plot from EFA for SSD-12.

Fig 4

The single-factor model suggested by exploratory factor analysis was further tested using single-factor measurement model in the AMOS program [32], however, the indices indicated lack of fit (see Fig 3).

Discussion

The DSM-5 outlines three criteria for diagnosing somatic symptom disorder among which Criterion-B deals with its manifestations through disproportionate thoughts, feelings, and behaviors related to somatic symptoms. Although the Structured Clinical Interview for DSM-5 (SCID-5) [36] is considered the standard method for the diagnosis of somatic symptoms, it is often taxing for clinicians to evaluate the B criteria in daily clinical work due to its time-consuming nature and inflexibility in clinical settings [20]. Diagnosing and treating somatically preoccupied patients is challenging, as they often prioritize physical concerns over psychological and social issues. In addition, it is crucial to address comorbid conditions such as substance abuse, depression, and anxiety. Due to the competing demands of treating and managing multiple conditions in the same patients, primary care practitioners often find it taxing to diagnose and manage patients with somatic symptom disorders [37]. Diagnosing these disorders thus presents significant challenges and requires comprehensive skills and knowledge of the biopsychosocial spectrum [37]. Consequently, patients with somatic symptom disorders are frequently referred from primary care to multiple specialists, creating a challenging cycle that is difficult to break. This inefficient use of resources can hinder appropriate care and exacerbate further patients’ symptoms and sufferings [38].

In Bangladesh, no other instruments are available that directly assess the three features of DSM-5 Somatic Symptom Disorder, particularly for criterion B somatic symptoms. Therefore, this study aimed to translate and validate the Bangla version of the SSD-12 to aid in the prompt diagnosis and assessment of therapeutic outcomes.

The findings demonstrated that the Bangla SSD-12 is a reliable and valid instrument for assessing somatic symptom disorder. Correlations between the SSD-12 scores and measures of somatic complaints, anxiety, and depression were moderate to high, affirming the test’s criterion and construct validity of the instrument. The findings are aligned with validation studies conducted in other Asian and European countries [20, 3941]. A unique feature of the present study is that it also demonstrated the SSD-12’s ability to discriminate between clinical and non-clinical samples (t198 = 16.74, p < .01) adding further support for its criterion validity. The ROC analysis indicates excellent diagnostic performance (area under the curve .936) of the SSD-12. With an optimal cutoff score of 22, the scale demonstrates acceptable sensitivity (89%) and specificity (84%). Similar values for cutoff and corresponding sensitivity and specificity of the has been reported in other contexts too [39].

The comorbidity of depression and anxiety with somatization is well-known [29]. Therefore, to measure convergent validity, the HADS with its anxiety and depression subscales was used. In line with previous study findings, [29, 39] the Bangla SSD-12 also demonstrated strong convergent validity through high correlations with the HADS and its subscales.

The Cronbach’s alpha (.94) of the Bangla version of the SSD-12 indicates strong internal consistency of the tool. It may be noted here that Cronbach’s alpha is highly influenced by the number of items in the measure. Therefore, a high alpha for a moderate-length (12-item) tool is a clear indication of the truly strong internal consistency of the Bangla SSD-12. Additionally, the split-half reliability (spearman r = .95) and the corrected item-total correlation (r = .46 to .82 for individual items) provide further support to its internal consistency reliability. The high internal consistency reliability of the Bangla SSD-12 is consistent with the original instrument [20] and other validation studies [39, 41]. These findings collectively support the robustness and reliability of the Bangla version of the SSD-12 in the Bangladesh context.

While most of the previous studies have supported a three-factor model (i.e., cognitive, affective, and behavioral) for the SSD-12 [20, 39], confirmatory factor analysis with Bangladesh data indicated a lack of fit across all indices using the stringent fit criteria suggested in recent validation studies conducted in the context [33]. Subsequent, exploratory factor analysis, identified a single-factor structure explaining 61.29% of the total variance. The single-factor structure of the tool was also reported in the Dutch context [41]. When the single-factor measurement model was put to the test using the present data, it did not show model fit on the indices. The divergence between EFA and CFA results is not uncommon in psychometric research [42, 43]. Being exploratory, EFA tends to identify dominant patterns within the data, which may oversimplify complex structures [44]. In contrast, CFA imposes strict constraints, such as requiring all items to load exclusively onto a single factor and setting non-target loadings to zero, making it more sensitive to model misspecifications [43]. These methodological differences may explain why the single-factor model identified in the EFA failed to achieve acceptable fit in the CFA. The differences in the factor structure between Bangladesh and other countries warrant further investigation to understand the universality of item interpretations.

The Bangla SSD-12 exhibits excellent psychometric properties comparable to other instruments available for assessing somatic symptoms, such as the Bangla Morey’s Somatic Complaints Scale [25]. Adequate psychometric properties are important features contributing to the confident use of any instrument. Translated instruments with psychometric properties similar to the Bangla SSD-12, such as the Perceived Stress Scale [33], the Bangla Mindful Attention Awareness Scale [45] and the Bangla WHO-5 Well-being Index [46] are being widely used in Bangladesh. Therefore, it is also likely that the Bangla SSD-12 will be accepted among researchers and clinicians in Bangladesh.

One of the constraints in this study was the use of a small sample size. However, a sample size of 200 in this analysis can be statistically justified as it is far above the suggested sample size based on the minimum subject-to-item ratio of 5:1[47]. The clinical sample was drawn from three tertiary referral hospitals situated in the country’s capital with the assumption that the sample would reflect participants from across the country. Exploring the SSD-12’s utility as a screening tool in primary care settings and its predictive capabilities would be valuable. To establish its screening and severity norm, participants from a wider range of geographic regions within the country can be used in future research. Collecting evidence of validity is an ongoing process for psychological instruments. Further work on the validation of the Bangla SSD-12 will enhance its robustness as well as confidence among its users regarding the utility of the instrument.

Conclusions

The thorough process followed in translating the SSD-12 in Bangla contributed to the strong psychometric properties that established it as a reliable and valid instrument. It is expected to fill the gap in the assessment and monitoring of somatic symptom disorder in clinical as well as research contexts. The SSD-12 being a fast and easy to administer tool, appeals for its use as a practical tool in hectic clinical environments. The use of this tool can be ultimately linked with improved patient outcomes. Future research should explore the scale’s applicability in diverse clinical populations within the region and its potential for tracking and providing feedback related to treatment outcomes.

Data Availability

The complete dataset used in this publication are available at https://doi.org/10.17605/OSF.IO/RH5BK.

Funding Statement

Collection of data was partially funded by Bangladesh National Science and Technology (NST) Fellowship received by SH. However, the author(s) did not receive any funding for preparing or publishing the manuscript.

References

  • 1.Creed F, Henningsen P, Fink P. Medically unexplained symptoms, somatisation and bodily distress: developing better clinical services: Cambridge University Press; 2011. [Google Scholar]
  • 2.American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 5th Edition: DSM 5. 5th ed: American Psychiatric Association; 2013. [Google Scholar]
  • 3.World Health Organization. International Classification of Diseases 11th Revision. 11th ed: World Health Organization,; 2019. [Google Scholar]
  • 4.Rice AS, Smith BH, Blyth FM. Pain and the global burden of disease. Pain. 2016;157(4):791–6. doi: 10.1097/j.pain.0000000000000454 [DOI] [PubMed] [Google Scholar]
  • 5.American Psychiatric Association. Diagnostic and statistical manual of mental disorders. Text revision. 2000. [Google Scholar]
  • 6.Barsky AJ, Cleary PD, Wyshak G, Spitzer RL, Williams JB, Klerman GL. A structured diagnostic interview for hypochondriasis: a proposed criterion standard. The Journal of nervous and mental disease. 1992;180(1):20–7. [DOI] [PubMed] [Google Scholar]
  • 7.Nair SS, Kwan SC, Ng CWM, Teo DCL. Approach to the patient with multiple somatic symptoms. Singapore Med J. 2021;62(5):252–8. doi: 10.11622/smedj.2021059 ; PubMed Central PMCID: PMC8801865. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Mullick M. Somatoform disorders in children and adolescents. Bangladesh Medical Research Council Bulletin. 2002;28(3):112–22. [PubMed] [Google Scholar]
  • 9.Beutel ME, Wiltink J, Ghaemi Kerahrodi J, Tibubos AN, Brähler E, Schulz A, et al. Somatic symptom load in men and women from middle to high age in the Gutenberg Health Study—association with psychosocial and somatic factors. Scientific Reports. 2019;9(1):4610. doi: 10.1038/s41598-019-40709-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Olesen J, Gustavsson A, Svensson M, Wittchen HU, Jönsson B, Group CS, et al. The economic cost of brain disorders in Europe. European journal of neurology. 2012;19(1):155–62. doi: 10.1111/j.1468-1331.2011.03590.x [DOI] [PubMed] [Google Scholar]
  • 11.DGHS. National Mental Health Survey of Bangladesh, 2018–2019: Provisional Fact Sheet DGHS, Bangladesh, 2019.
  • 12.Mohit M. Diagnosis of patients attending Out Patient Department (OPD) of NIMH. Bang J Psychiatry. 2001;15(1):5–12. [Google Scholar]
  • 13.Kroenke K, Spitzer RL, deGruy FV III, Hahn SR, Linzer M, Williams JBW, et al. Multisomatoform Disorder: An Alternative to Undifferentiated Somatoform Disorder for the Somatizing Patient in Primary Care. Archives of General Psychiatry. 1997;54(4):352–8. doi: 10.1001/archpsyc.1997.01830160080011 [DOI] [PubMed] [Google Scholar]
  • 14.Dimsdale JE, Dantzer R. A biological substrate for somatoform disorders: importance of pathophysiology. Psychosom Med. 2007;69(9):850–4. doi: 10.1097/PSY.0b013e31815b00e7 ; PubMed Central PMCID: PMC2908292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Juul SH, Nemeroff CB. Chapter 10—Psychiatric epidemiology†. In: Aminoff MJ, Boller F, Swaab DF, editors. Handbook of Clinical Neurology. 106: Elsevier; 2012. p. 167–89. [DOI] [PubMed] [Google Scholar]
  • 16.Smith GR Jr, Monson RA, Ray DC. Patients With Multiple Unexplained Symptoms: Their Characteristics, Functional Health, and Health Care Utilization. Archives of Internal Medicine. 1986;146(1):69–72. doi: 10.1001/archinte.1986.00360130079012 [DOI] [PubMed] [Google Scholar]
  • 17.Smith JK, Józefowicz RF. Diagnosis and treatment of somatoform disorders. Neurology Clinical Practice. 2012;2(2):94–102. doi: 10.1212/CPJ.0b013e31825a6183 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.olde Hartman TC, Borghuis MS, Lucassen PLBJ, van de Laar FA, Speckens AE, van Weel C. Medically unexplained symptoms, somatisation disorder and hypochondriasis: Course and prognosis. A systematic review. Journal of Psychosomatic Research. 2009;66(5):363–77. 10.1016/j.jpsychores.2008.09.018. [DOI] [PubMed] [Google Scholar]
  • 19.Creed F, Barsky A. A systematic review of the epidemiology of somatisation disorder and hypochondriasis. Journal of Psychosomatic Research. 2004;56(4):391–408. doi: 10.1016/S0022-3999(03)00622-6 [DOI] [PubMed] [Google Scholar]
  • 20.Toussaint A, Murray AM, Voigt K, Herzog A, Gierk B, Kroenke K, et al. Development and Validation of the Somatic Symptom Disorder–B Criteria Scale (SSD-12). Psychosomatic Medicine. 2016;78(1):5–12. doi: 10.1097/PSY.0000000000000240 [DOI] [PubMed] [Google Scholar]
  • 21.Rief W, Martin A. How to Use the New DSM-5 Somatic Symptom Disorder Diagnosis in Research and Practice: A Critical Evaluation and a Proposal for Modifications. Annual Review of Clinical Psychology. 2014;10(1):339–67. doi: 10.1146/annurev-clinpsy-032813-153745 [DOI] [PubMed] [Google Scholar]
  • 22.Derogatis LR. Symptoms checklist-90. Administration, scoring, and procedures manual for the revised version. 1977. [Google Scholar]
  • 23.Kroenke K, Spitzer RL, Williams JB. The PHQ-15: validity of a new measure for evaluating the severity of somatic symptoms. Psychosomatic medicine. 2002;64(2):258–66. doi: 10.1097/00006842-200203000-00008 [DOI] [PubMed] [Google Scholar]
  • 24.First MB, Williams JB, Karg RS, Spitzer RL. User’s guide for the SCID-5-CV Structured Clinical Interview for DSM-5® disorders: Clinical version: American Psychiatric Publishing, Inc.; 2016. [Google Scholar]
  • 25.Uddin MK, Khatun H, Ferdous J, Choudhury SA. Cultural Adaptation of the Morey‟ s Somatic Complaints Scale for use in Bangladesh. Bangladesh Journal of Psychology. 2020;23:135–52. [Google Scholar]
  • 26.Morey L. Personality Assessment Inventory. Florida: PAR Psychological Assessment Resources. Inc [Google Scholar]. 1991. [Google Scholar]
  • 27.Zigmond AS, Snaith RP. The hospital anxiety and depression scale. Acta psychiatrica scandinavica. 1983;67(6):361–70. doi: 10.1111/j.1600-0447.1983.tb09716.x [DOI] [PubMed] [Google Scholar]
  • 28.Bjelland I, Dahl AA, Haug TT, Neckelmann D. The validity of the Hospital Anxiety and Depression Scale: an updated literature review. Journal of psychosomatic research. 2002;52(2):69–77. [DOI] [PubMed] [Google Scholar]
  • 29.Löwe B, Spitzer RL, Williams JB, Mussell M, Schellberg D, Kroenke K. Depression, anxiety and somatization in primary care: syndrome overlap and functional impairment. General hospital psychiatry. 2008;30(3):191–9. doi: 10.1016/j.genhosppsych.2008.01.001 [DOI] [PubMed] [Google Scholar]
  • 30.International Test Commission. ITC Guidelines for Translating and Adapting Tests (Second Edition). International Journal of Testing. 2018;18(2):101–34. doi: 10.1080/15305058.2017.1398166 [DOI] [Google Scholar]
  • 31.Mostafaei S, Kabir K, Kazemnejad A, Feizi A, Mansourian M, Hassanzadeh Keshteli A, et al. Explanation of somatic symptoms by mental health and personality traits: application of Bayesian regularized quantile regression in a large population study. BMC psychiatry. 2019;19(1). doi: 10.1186/s12888-019-2189-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Arbuckle JL. Amos 18. 18 ed. Crawfordville, Florida: Amos Development Corporation; 2009. [Google Scholar]
  • 33.Mozumder MK. Reliability and validity of the Perceived Stress Scale in Bangladesh. PloS one. 2022;17(10):e0276837. doi: 10.1371/journal.pone.0276837 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Kaiser HF. A second generation little jiffy. 1970. [Google Scholar]
  • 35.Fidell LS. Using multivariate statistics: Allyn and Bacon; 2001. [Google Scholar]
  • 36.First MB. Structured Clinical Interview for the (SCID). The Encyclopedia of Clinical Psychology 2015. p. 1–6. [Google Scholar]
  • 37.Murray AM, Toussaint A, Althaus A, Löwe B. The challenge of diagnosing non-specific, functional, and somatoform disorders: A systematic review of barriers to diagnosis in primary care. Journal of Psychosomatic Research. 2016;80:1–10. doi: 10.1016/j.jpsychores.2015.11.002 [DOI] [PubMed] [Google Scholar]
  • 38.Bass C, May S. Chronic multiple functional somatic symptoms. BMJ. 2002;325(7359):323–6. doi: 10.1136/bmj.325.7359.323 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Li T, Wei J, Fritzsche K, Toussaint AC, Jiang Y, Cao J, et al. Validation of the Chinese Version of the Somatic Symptom Disorder–B Criteria Scale for Detecting DSM-5 Somatic Symptom Disorders: A Multicenter Study. Psychosomatic Medicine. 2020;82(3):337–44. doi: 10.1097/PSY.0000000000000786 [DOI] [PubMed] [Google Scholar]
  • 40.Salma S, Kahija YFL, Rahmandani A. Reliability and Factorial Structure of Indonesian Version of the Somatic Symptom Disorders–B Criteria Scale (SSD-12) in Undergraduate Students Sample. Proceedings of International Conference on Psychological Studies (ICPsyche). 2023;4(1):165–74. doi: 10.58959/icpsyche.v4i1.34 [DOI] [Google Scholar]
  • 41.Kop WJ, Toussaint A, Mols F, Löwe B. Somatic symptom disorder in the general population: Associations with medical status and health care utilization using the SSD-12. General Hospital Psychiatry. 2019;56:36–41. doi: 10.1016/j.genhosppsych.2018.10.004 [DOI] [PubMed] [Google Scholar]
  • 42.Brown TA. Confirmatory factor analysis for applied research. 2nd ed. New York: Guilford publications; 2015. [Google Scholar]
  • 43.Marsh HW, Hau K-T, Wen Z. In search of golden rules: Comment on hypothesis-testing approaches to setting cutoff values for fit indexes and dangers in overgeneralizing Hu and Bentler’s (1999) findings. Structural Equation Modeling. 2004;11(3):320–41. [Google Scholar]
  • 44.Worthington RL, Whittaker TA. Scale Development Research:A Content Analysis and Recommendations for Best Practices. The Counseling Psychologist. 2006;34(6):806–38. doi: 10.1177/0011000006288127 [DOI] [Google Scholar]
  • 45.Islam MA, Siddique S. Validation of the Bangla Mindful Attention Awareness Scale. Asian Journal of Psychiatry. 2016;24:10–6. doi: 10.1016/j.ajp.2016.08.011 [DOI] [PubMed] [Google Scholar]
  • 46.Faruk MO, Alam F, Chowdhury KUA, Soron TR. Validation of the Bangla WHO-5 Well-being Index. Global Mental Health. 2021;8:e26. Epub 2021/07/19. doi: 10.1017/gmh.2021.26 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Gorsuch RL. Factor Analysis. Hillsdale, NJ: Lawrence Earlbaum Associates. Inc; 1983. [Google Scholar]

Decision Letter 0

Kenta Matsumura

26 Nov 2024

PONE-D-24-42215Validation of the Somatic Symptom Disorder - B Criteria Scale (SSD-12) in BangladeshPLOS ONE

Dear Dr. Mozumder,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

As a point to note, when revising your paper, please respond to all comments.

Please submit your revised manuscript by Jan 10 2025 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Kenta Matsumura

Academic Editor

PLOS ONE

Journal requirements:

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2. Thank you for stating the following financial disclosure: [Collection of data was partially funded by Bangladesh National Science and Technology (NST) Fellowship received by SH. However, the author(s) did not receive any funding for preparing or publishing the manuscript.]. At this time, please address the following queries: a) Please clarify the sources of funding (financial or material support) for your study. List the grants or organizations that supported your study, including funding received from your institution. b) State what role the funders took in the study. If the funders had no role in your study, please state: “The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.” c) If any authors received a salary from any of your funders, please state which authors and which funders. d) If you did not receive any funding for this study, please state: “The authors received no specific funding for this work.” Please include your amended statements within your cover letter; we will change the online submission form on your behalf.

3. Please include your full ethics statement in the ‘Methods’ section of your manuscript file. In your statement, please include the full name of the IRB or ethics committee who approved or waived your study, as well as whether or not you obtained informed written or verbal consent. If consent was waived for your study, please include this information in your statement as well.

Additional Editor Comments:

I understand that it is not the original three-factor structure, but a one-factor structure. However, because the description of this verification process is omitted, I cannot judge whether the results support the conclusion. Therefore, I request the following items be added.

- Presentation of the scree plot

- Report of each fit index when applying CFA to the one-factor structure (please be careful not to set correlation between errors when analyzing)

The authors state that cases can be discriminated based on the results of the t-test, but ROC analysis would be more appropriate here. Therefore, please add the following.

- ROC (figure)

- Typical values such as AUC and its 95% confidence interval, sensitivity, specificity, positive predictive value, etc.

Other

・If possible, please state the effect size

・L154: “α” —> “p”?

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: This study represents an important step toward the diagnosis of Somatic Symptom Disorder. However, I believe some revisions are necessary to enhance its clarity and impact.

General Comments

I recommend providing a more comprehensive description of Somatic Symptom Disorder to contextualize the study. Including the following information will help convey the significance and importance of this research.

Abstract

Please ensure consistency in terminology throughout the paper. For example, on lines 18 and 19, the terms "Non-clinical" and "nonclinical" are used interchangeably. Standardizing the format will improve readability and precision.

Introduction

A more detailed explanation of the three diagnostic criteria for Somatic Symptom Disorder is needed. Additionally, I recommend including the following information:

Typical symptoms

Prevalence rates

Comorbidities with other psychiatric disorders

Specific disease names and characteristics of individuals prone to developing the disorder

Treatment duration, methods, and prognosis

Providing these details will offer readers a clearer and more comprehensive understanding of the disorder.

Methods

Demographic Details: Include information about the average duration of Somatic Symptom Disorder in the clinical group (e.g., mean value, standard deviation). Address potential biases in the patient groups across the three facilities.

Questionnaire Details: Incorporate some of the specific questions and characteristics from the three domains of Somatic Symptom Disorder in the text, not just in the tables, to enhance clarity.

Instructions to Respondents: Provide information on the instructions given to respondents. For instance, clarify whether participants were asked to answer based on their experiences over the past week or the past few days.

Discussion

You mention that diagnosing criterion B is burdensome, but only one study is cited to support this claim. I recommend:

Discussing this study in more detail to provide a stronger foundation for your argument.

Including additional relevant citations to strengthen the discussion.

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Mariko Inoue

**********

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2025 Jan 24;20(1):e0318062. doi: 10.1371/journal.pone.0318062.r002

Author response to Decision Letter 0


8 Jan 2025

Response to Reviewer Comments to the Author

A. Reviewer #1:

This study represents an important step toward the diagnosis of Somatic Symptom Disorder. However, I believe some revisions are necessary to enhance its clarity and impact.

We sincerely thank you for your thoughtful comments and valuable suggestions to improve our manuscript. We have carefully addressed each of your points and made corresponding revisions to the manuscript as detailed below.

General Comments: I recommend providing a more comprehensive description of Somatic Symptom Disorder to contextualize the study. Including the following information will help convey the significance and importance of this research.

Response: We have revised the introduction section thoroughly as per this and other comments and we believe it now covers a more comprehensive description of Somatic Symptom Disorder to contextualize the study.

Abstract: Please ensure consistency in terminology throughout the paper. For example, in lines 18 and 19, the terms "Non-clinical" and "nonclinical" are used interchangeably. Standardizing the format will improve readability and precision.

Response: Thank you for noticing this inconsistency. We have checked the manuscript and changed all such instances to "non-clinical" for consistency.

Introduction: A more detailed explanation of the three diagnostic criteria for Somatic Symptom Disorder is needed. Additionally, I recommend including the following information:

Typical symptoms

Prevalence rates

Comorbidities with other psychiatric disorders

Specific disease names and characteristics of individuals prone to developing the disorder

Treatment duration, methods, and prognosis

Providing these details will offer readers a clearer and more comprehensive understanding of the disorder.

Response: We appreciate this suggestion and have expanded the Introduction section to include a more detailed description of Somatic Symptom Disorder (SSD). The following details have been added to the introduction section.

Somatization is generally characterized by three distinct features [6]. Firstly, it presents with medically unexplained somatic symptoms such as pain, weakness, or shortness of breath, Secondly, patients exhibit somatic preoccupation or hypochondriacal worry, demonstrating excessive engagement (in terms of time and effort) and concerns about their bodily symptoms. These concerns are often overtly disproportionate and may be accompanied by excessive body checking and reassurance-seeking [7]. Thirdly, patients may present these somatic symptoms as part of the clinical manifestations of anxiety, affective, or other psychiatric disorders [6]. (see page 3)

Somatization may present with a range of symptoms, Bangladeshi children and adolescents diagnosed with somatoform disorder report an average of 12 to 16 somatic symptoms [15]. Pain is the most common symptom among patients. In Bangladesh, abdominal pain is the most frequent somatic symptom in children and adolescents, while a German study of 7,925 adults aged 40 to 80 years found that pain complaints (arms, legs, joints, back pain) were most common, followed by back pain, headaches, nausea, constipation/diarrhea, shortness of breath, dizziness, and heart racing or pounding. (see page 4)

Across the globe, including Bangladesh, somatic symptom disorders have been reported to be the third most prevalent mental disorders followed by depression and anxiety [10]. (see page 4)

Somatoform disorders are among the most common psychiatric disorders in general medical settings. Somatoform disorders often coexist with other comorbidities, with 8% of primary care patients meeting the criteria for 'multi-somatoform disorder’[13]. Depression, conversion disorder, hypochondriasis, somatization, and pain disorders are the most common comorbid conditions associated with somatization[14]. Apart from comorbidity, somatization disorder has been reported to be associated strongly with depression and anxiety, moderately with schizophrenia and mania, and weakly with substance use and antisocial personality[15].(see page 4)

Accurate diagnosis, support, and reassurance are the cornerstones of the treatment of somatization disorder [16]. Approaches typically involve psychotropic medications and psychological therapies (such as cognitive behavior therapy) focusing on cognitive, emotional, and behavioral aspects [17]. The prognosis for somatic symptom disorder shows improvement in 50–75% of patients, while 10–30% experience a worsening of their condition under combination treatment (medication and psychological therapy)[18]. Fewer symptoms and higher baseline functioning have been linked with a better prognosis [19]. (see page 4-5)

Methods

Demographic Details: Include information about the average duration of Somatic Symptom Disorder in the clinical group (e.g., mean value, standard deviation). Address potential biases in the patient groups across the three facilities.

Response: Unfortunately, we did not record the average duration of symptoms during data collection and hence are unable to present the suggested data. Thank you for your valuable comment it will help us improve data collection in future research. To address the bias, we have added the following details in the participant section.

Data for this study were collected from the psychiatric departments of three tertiary hospitals, providing access to a diverse patient population. For one of the hospitals, the majority of the data were collected from the inpatient department, while for another, the majority came from the outpatient department. These differences may result in inadvertent variation in the patient groups across the three settings. However, as no comparisons between the settings were planned, we believe these variations contribute to the generalizability of the findings. (see page 7)

Questionnaire Details: Incorporate some of the specific questions and characteristics from the three domains of Somatic Symptom Disorder in the text, not just in the tables, to enhance clarity.

Response: We agree with this suggestion and have included sample questions from the three domains (somatic symptoms, excessive thoughts, and behaviors) directly in the Instruments section to enhance clarity.

The respondents report their experiences of cognition, emotion, or behavior on a 5-point Likert scale such as, “I think that my physical symptoms are signs of a serious illness”, “I am very worried about my health”, “My health concerns hinder me in everyday life”. (see page 7)

Instructions to Respondents: Provide information on the instructions given to respondents. For instance, clarify whether participants were asked to answer based on their experiences over the past week or the past few days.

Response: We have clarified the instructions provided to participants in the Instruments section.

Participants were instructed to complete the SSD-12 questionnaire based on their experiences over the past week, aiming to capture the severity of recent symptoms and their impact. (see page 7)

Discussion: You mention that diagnosing criterion B is burdensome, but only one study is cited to support this claim. I recommend: Discussing this study in more detail to provide a stronger foundation for your argument. Including additional relevant citations to strengthen the discussion.

Response: We have expanded the discussion of the cited study to better support the claim regarding the burden of diagnosing criterion B. Additionally, we have included two more relevant studies to strengthen this point.

Diagnosing and treating somatically preoccupied patients is challenging, as they often prioritize physical concerns over psychological and social issues. In addition, it is crucial to address comorbid conditions such as, substance abuse, depression, and anxiety. Due to the competing demands of treating and managing multiple conditions in the same patients, primary care practitioners often find it taxing to diagnose and manage patients with somatic symptom disorders [37]. Diagnosing these disorders thus presents significant challenges and requires comprehensive skills and knowledge of the biopsychosocial spectrum [37]. Consequently, patients with somatic symptom disorders are frequently referred from primary care to multiple specialists, creating a challenging cycle that is difficult to break. This inefficient use of resources can hinder appropriate care and exacerbate further patients' symptoms and sufferings [38]. (see page 15-16)

B. Editor Comments

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming.

Response: We have checked manuscript again for PLOS One’s style requirements.

2. Thank you for stating the following financial disclosure: [Collection of data was partially funded by Bangladesh National Science and Technology (NST) Fellowship received by SH. However, the author(s) did not receive any funding for preparing or publishing the manuscript.]. At this time, please address the following queries: a) Please clarify the sources of funding (financial or material support) for your study. List the grants or organizations that supported your study, including funding received from your institution. b) State what role the funders took in the study. If the funders had no role in your study, please state: “The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.” c) If any authors received a salary from any of your funders, please state which authors and which funders. d) If you did not receive any funding for this study, please state: “The authors received no specific funding for this work.” Please include your amended statements within your cover letter; we will change the online submission form on your behalf.

Response: Thank you for providing detailed instructions regarding the financial disclosure statement. We have amended it accordingly and added the following text in the cover letter.

Our study was partially funded by the National Science and Technology (NST) Fellowship, from the Ministry of Science and Technology, Government of Bangladesh awarded to SH. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors received no specific funding for this work.

3. Please include your full ethics statement in the ‘Methods’ section of your manuscript file. In your statement, please include the full name of the IRB or ethics committee who approved or waived your study, as well as whether or not you obtained informed written or verbal consent. If consent was waived for your study, please include this information in your statement as well.

Response: We have updated the Methods section of the manuscript to include the full ethics statement, as follows:

All the participants provided written informed consent. The project received ethical approval prior to data collection from the Ethics Committee of the Department of Clinical Psychology, University of Dhaka (protocol# MS210504, approved on 18 May 2021). (see page 9)

Additional Editor Comments: I understand that it is not the original three-factor structure, but a one-factor structure. However, because the description of this verification process is omitted, I cannot judge whether the results support the conclusion. Therefore, I request the following items be added.

- Presentation of the scree plot

Response: Added as Fig 4. (see page 15)

- Report of each fit index when applying CFA to the one-factor structure (please be careful not to set correlation between errors when analyzing)

Response: We have added a description of the verification process for the one-factor structure, including a scree plot and fit indices (CFI, TLI, RMSEA, SRMR) obtained from the CFA analysis. Correlations between errors were not set, as per the suggestion.

A new figure (Fig 3) depicting the single-factor as well as the three-factor model has been added along with a new table (Table 4) to accommodate the suggestion. Additionally the following texts has been added in result section (see page 15).

The single-factor model suggested by exploratory factor analysis was further tested using single-factor measurement model in the AMOS program [32], however, the indices indicated lack of fit (see Fig 3). (see page 15)

The discussion section has also been updated with the following texts (see page -18).

When the single-factor measurement model was put to the test using the present data, it did not show model fit on the indices. The divergence between EFA and CFA results is not uncommon in psychometric research [42, 43]. Being exploratory, EFA tends to identify dominant patterns within the data, which may oversimplify complex structures [44]. In contrast, CFA imposes strict constraints, such as requiring all items to load exclusively onto a single factor and setting non-target loadings to zero, making it more sensitive to model misspecifications [43]. These methodological differences may explain why the single-factor model identified in the EFA failed to achieve acceptable fit in the CFA. (see page 18)

The authors state that cases can be discriminated based on the results of the t-test, but ROC analysis would be more appropriate here.

Response: As per suggestion we have added ROC analysis and relevant texts has been added as follows.

In the result section (see page 10 )

Additionally, to assess the diagnostic accuracy of the SSD-12, the Receiver Operating Characteristic (ROC) curve was used (Fig 2).

The area under the curve was .936 (95% CI [.903, .969], p < .01), indicating excellent diagnostic performance. The sensitivity-specificity calculation suggests the optimal cutoff score of 22 with a sensitivity of 0.89 and a specificity of 0.84 (Table 2). (see page 10)

And in the discussion section (see page 17)

The ROC analysis indicates excellent diagnostic performance (area under the curve .936) of the SSD-12. With an optimal cutoff score of 22, the scale demonstrates acceptable sensitivity (89%) and specificity (84%). Similar values for cutoff and corresponding sensitivity and specificity of the has been reported in other contexts too [39]. (see page 17)

Therefore, please add the following.

- ROC (figure)

Response: ROC (figure) has been added as per suggestion (Fig 2.; page 10).

- Typical values such as AUC and its 95% confidence interval, sensitivity, specificity, positive predictive value, etc.

Response: These have been added as per suggestions please see response to earlier comment). We have also added a table (Table 2) to present the sensitivity and specificity. (see page 11)

Other

・If possible, please state the effect size

Response: We have added effect size estimates (Cohen’s d) as per suggestions in Table 1 (see page 10)

・L154: “α” —> “p”?

Response: We sincerely apologize for the typos, and these have been corrected as per suggestion. Subsequently, we ran checks throughout the whole manuscript again for errors in texts and numbers and realized that we did not update few data values while preparing the draft. We have corrected those inadvertent mistakes too.

Attachment

Submitted filename: Response to Reviewers.docx

pone.0318062.s001.docx (28.4KB, docx)

Decision Letter 1

Kenta Matsumura

10 Jan 2025

Validation of the Somatic Symptom Disorder - B Criteria Scale (SSD-12) in Bangladesh

PONE-D-24-42215R1

Dear Dr. Mozumder,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice will be generated when your article is formally accepted. Please note, if your institution has a publishing partnership with PLOS and your article meets the relevant criteria, all or part of your publication costs will be covered. Please make sure your user information is up-to-date by logging into Editorial Manager at Editorial Manager® and clicking the ‘Update My Information' link at the top of the page. If you have any questions relating to publication charges, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Kenta Matsumura

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Acceptance letter

Kenta Matsumura

14 Jan 2025

PONE-D-24-42215R1

PLOS ONE

Dear Dr. Mozumder,

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now being handed over to our production team.

At this stage, our production department will prepare your paper for publication. This includes ensuring the following:

* All references, tables, and figures are properly cited

* All relevant supporting information is included in the manuscript submission,

* There are no issues that prevent the paper from being properly typeset

If revisions are needed, the production department will contact you directly to resolve them. If no revisions are needed, you will receive an email when the publication date has been set. At this time, we do not offer pre-publication proofs to authors during production of the accepted work. Please keep in mind that we are working through a large volume of accepted articles, so please give us a few weeks to review your paper and let you know the next and final steps.

Lastly, if your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

If we can help with anything else, please email us at customercare@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Kenta Matsumura

Academic Editor

PLOS ONE

Attachment

Submitted filename: pone.0318062.docx

pone.0318062.s002.docx (53KB, docx)

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    Attachment

    Submitted filename: Response to Reviewers.docx

    pone.0318062.s001.docx (28.4KB, docx)
    Attachment

    Submitted filename: pone.0318062.docx

    pone.0318062.s002.docx (53KB, docx)

    Data Availability Statement

    The complete dataset used in this publication are available at https://doi.org/10.17605/OSF.IO/RH5BK.


    Articles from PLOS ONE are provided here courtesy of PLOS

    RESOURCES