International Journal of Medical and Pharmaceutical Research
2026, Volume-7, Issue 4 : 1123-1132
Research Article
Significance and Analysis of Stressors in Young Females with Suicidal Risk
 ,
Received
May 25, 2026
Accepted
July 7, 2026
Published
July 15, 2026
Abstract

Background: Multidimensional stress plays a key role in suicidal risk among young females with mild to moderate depression. This study compared the effectiveness of pharmacotherapy alone with pharmacotherapy combined with dimension-based psychotherapy in reducing stress burden.

Methods: In this prospective randomized hospital-based study, 75 females (18–35 years) with DSM-5 diagnosed mild to moderate depression (HAM-D 10–18) and suicidal ideation, with or without a suicide attempt within the previous six months, were randomized to pharmacotherapy alone (n = 38) or pharmacotherapy plus dimension-based psychotherapy (n = 37). Stress was assessed at baseline and across eight follow-up visits using the Suicidal Stressor Diagnostic Questionnaire (SSDQ).

Results: Both groups showed significant reductions in cumulative stress load and SSDQ domain scores. However, the combined therapy group demonstrated significantly greater improvements in cumulative stress load and most stress domains than the pharmacotherapy-alone group (all p < 0.001).

Conclusion: Dimension-based psychotherapy enhances the effectiveness of pharmacotherapy by providing greater reduction in multidimensional stress burden among young females with suicidal risk, supporting its integration into routine clinical management.

Keywords
INTRODUCTION

Suicide is a major global public health concern and remains one of the leading causes of death among adolescents and young adults worldwide. Young females represent a particularly vulnerable population because they experience a high prevalence of suicidal ideation and suicide attempts, often in the context of emotional distress, interpersonal conflicts, academic pressures, and psychosocial adversities[1]. Although completed suicide rates are generally higher among males, suicidal thoughts, non-fatal suicide attempts, and help-seeking behaviours occur more frequently among young females, highlighting the need for early identification of modifiable psychosocial risk factors [2,3].Suicidal behaviour is a complex and multifactorial phenomenon resulting from the interaction of biological, psychological, social, and environmental factors rather than from a single precipitating event. Contemporary theoretical models suggest that stress, feelings of defeat, entrapment, and impaired coping mechanisms play central roles in the development of suicidal ideation and progression to suicidal behaviour[4]. During young adulthood, a developmental period characterized by academic, occupational, and interpersonal transitions, chronic or severe stress may impair emotional regulation, reduce resilience, increase hopelessness, and precipitate depressive symptoms, thereby substantially increasing suicidal vulnerability [5,6].Young females are exposed to a broad spectrum of stressors that extend beyond depressive symptomatology. Relationship difficulties, family conflict, social isolation, academic expectations, financial concerns, gender-related discrimination, body image dissatisfaction, traumatic life events, and emotional abuse frequently coexist and interact to amplify suicide risk [7]. Recent evidence indicates that psychosocial stressors, particularly interpersonal rejection and cumulative adverse life events, play a crucial role in the onset and persistence of suicidal ideation among young women. These observations emphasize that suicidal risk should be understood within a multidimensional psychosocial framework rather than solely as a manifestation of psychiatric illness [8,9].Previous research has consistently demonstrated that depression, anxiety, perceived stress, low self-esteem, poor resilience, maladaptive coping strategies, and a family history of suicidal behaviour are important predictors of suicidal risk in adolescents and young adults [10]. Furthermore, the cumulative burden of multiple psychosocial stressors appears to exert a greater influence on suicidal behaviour than any individual stressor alone. Consequently, comprehensive assessment of stress domains may facilitate earlier recognition of individuals at high risk and enable the development of targeted psychosocial interventions aimed at reducing suicidal behaviour [11,12].Despite increasing awareness regarding suicide prevention, relatively few studies have comprehensively examined the multidimensional pattern of stressors specifically among young females with suicidal risk, particularly in the Indian clinical setting. Most available research has primarily focused on depressive disorders or psychiatric diagnoses while providing limited insight into the relative contribution of individual psychosocial stress domains. Understanding these stress profiles is essential for developing individualized treatment strategies and implementing effective preventive interventions that extend beyond pharmacological management [13].

 

Therefore, the present study was undertaken to analyze the significance and distribution of multidimensional stressors among young females with suicidal risk.

 

MATERIALS AND METHODS

This prospective, randomized, comparative interventional study was conducted in the Department of Psychiatry, Institute of Medical Sciences (IMS), Banaras Hindu University (BHU), Varanasi, India, over a one-year period from April 2024 to March 2025. The study was designed to evaluate the significance of multidimensional stressors among young females with suicidal risk and to compare the effectiveness of pharmacotherapy alone with pharmacotherapy combined with dimension-based psychotherapy in reducing cumulative stress burden and improving stress-related domains over serial follow-up assessments.

 

Study Population

The study included female patients aged 18–35 years attending the Psychiatry Outpatient Department (OPD) or admitted to the Psychiatry inpatient services. Eligible participants fulfilled the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) diagnostic criteria for mild to moderate depressive disorder and had a baseline Hamilton Depression Rating Scale (HAM-D) score between 10 and 18. All participants presented with suicidal ideation, with or without a history of suicide attempt during the preceding six months.A total of 75 eligible participants were enrolled in the study. Participants were randomly allocated into two treatment groups: Group I (pharmacotherapy alone, n = 38) and Group II (pharmacotherapy plus dimension-based psychotherapy, n = 37).

 

Inclusion Criteria

  • Female patients aged 18–35 years.
  • DSM-5 diagnosis of mild to moderate depressive disorder.
  • Baseline HAM-D score between 10 and 18.
  • Presence of suicidal ideation, with or without suicide attempt within the previous six months.
  • Willingness to participate and provide written informed consent.

 

Exclusion Criteria

  • Severe depression (HAM-D >18).
  • Bipolar affective disorder, schizophrenia spectrum disorders, or other psychotic disorders.
  • Current substance dependence (except nicotine).
  • Severe neurological illness or major medical disorders affecting psychiatric assessment.
  • Intellectual disability or cognitive impairment.
  • Pregnancy or lactation.
  • Refusal to provide informed consent.

 

Sampling Technique and Randomization

Participants fulfilling the eligibility criteria were recruited using purposive sampling. Following enrolment, subjects were randomly allocated into two treatment arms using a computer-generated randomization sequence with allocation concealment through sealed opaque envelopes.

 

Study Intervention

Group I (Pharmacotherapy Alone)

Participants received standard pharmacological management consisting of Escitalopram (5–10 mg/day) with Clonazepam 0.5 mg administered on an SOS basis whenever clinically indicated. Proton pump inhibitors were prescribed where necessary.

Group II (Pharmacotherapy Plus Dimension-Based Psychotherapy)

Participants received the same pharmacological treatment as Group I along with structured dimension-based psychotherapy. The psychotherapeutic intervention was individualized according to the participant's multidimensional stress profile identified at baseline. The intervention included:

  • Deep breathing relaxation exercises.
  • Stress-management techniques for generalized cumulative stress.
  • Domain-specific counselling targeting behavioural, emotional, familial, interpersonal, personal, physical health, social, educational, and stress-coping domains.
  • Focused psychotherapy addressing independent high-salience stressors contributing to suicidal vulnerability.

 

Stress Assessment

Stress was evaluated using the Suicidal Stressor Diagnostic Questionnaire (SSDQ). Unlike conventional symptom-based assessment, the SSDQ enabled comprehensive evaluation of multidimensional stress by measuring:

  • Individual domain-wise stress scores.
  • Cumulative Stress Load (CSL), calculated as the sum of all SSDQ domain scores.
  • Independent high-salience stressors contributing disproportionately to suicidal risk.

The SSDQ domains included:

  • Behavioural (B)
  • Emotional Distress (ED)
  • Familial (F)
  • Interpersonal (IP)
  • Mood and Thought (M&T)
  • Personal (P)
  • Physical Health (PHY)
  • Social (S)
  • Stress Coping (SC)

 

Follow-up Assessment

Participants were assessed at baseline and subsequently followed through eight structured follow-up visits. At each follow-up, SSDQ domain scores and cumulative stress load were reassessed. Participants allocated to the psychotherapy group received reinforcement sessions focusing on individualized stress domains during each scheduled visit.

 

Outcome Measures

Primary outcome

  • Change in Cumulative Stress Load (CSL) from baseline across eight follow-up visits.

Secondary outcomes

  • Changes in individual SSDQ domain scores:
    • Behavioural
    • Emotional Distress
    • Familial
    • Interpersonal
    • Mood and Thought
    • Personal
    • Physical Health
    • Social
    • Stress Coping
  • Comparison of stress reduction between treatment groups throughout follow-up.

 

Ethical Considerations

The study protocol was approved by the Institutional Ethics Committee, Institute of Medical Sciences, Banaras Hindu University, Varanasi. Written informed consent was obtained from all participants prior to enrolment. Confidentiality of participant information was maintained throughout the study, and all procedures were conducted in accordance with the ethical principles of the Declaration of Helsinki.

 

Statistical Analysis

Data were entered into Microsoft Excel and analyzed using IBM SPSS Statistics version 26.0 (IBM Corp., Armonk, NY, USA). Continuous variables were expressed as mean ± standard deviation (SD), whereas categorical variables were presented as frequencies and percentages.Baseline inter-group comparisons were performed using the independent samples t-test. Changes within each treatment group from baseline to successive follow-up visits were analyzed using the paired t-test. A two-tailed p-value of <0.05 was considered statistically significant throughout the analysis.

 

RESULTS

A total of 75 young females with mild to moderate depression and suicidal ideation were included in the study. Of these, 38 participants received pharmacotherapy alone, while 37 participants received pharmacotherapy combined with dimension-based psychotherapy. All participants completed the scheduled follow-up assessments.Baseline cumulative stress load (CSL) was comparable between the pharmacotherapy and combined therapy groups (215.52 ± 38.91 vs. 212.08 ± 36.44, p=0.653). Both groups demonstrated significant reductions in CSL compared with baseline at every follow-up assessment (p<0.001 for all intra-group comparisons). Inter-group differences became statistically significant from the third follow-up onward, with participants receiving pharmacotherapy plus dimension-based psychotherapy showing progressively greater reductions in cumulative stress load than those receiving pharmacotherapy alone (p<0.001 through the eighth follow-up). At the final follow-up, mean CSL decreased to 110.36 ± 25.64 in the pharmacotherapy group and 59.72 ± 17.83 in the combined therapy group (p<0.001) (Table 1, Figure 1).Behavioural stress scores were similar at baseline between the two groups (p=0.429). Significant reductions from baseline were observed in both groups throughout follow-up. Although improvements occurred in both treatment arms, participants receiving adjunctive psychotherapy demonstrated significantly greater reductions from the third follow-up onward, with highly significant differences during later assessments (p<0.001). By the eighth follow-up, behavioural scores declined from 38.04 ± 10.11 to 8.52 ± 7.05 in the pharmacotherapy group and from 36.50 ± 9.26 to 6.28 ± 6.05 in the combined therapy group (Table 2, Figure 2).Baseline emotional distress scores were comparable between groups (p=0.280). Both treatment groups exhibited significant reductions over time. Inter-group differences became significant during later follow-up visits, with the combined therapy group demonstrating greater improvement. At the eighth follow-up, emotional distress scores were significantly lower in the combined therapy group than in the pharmacotherapy group (15.18 ± 7.80 vs. 18.27 ± 7.62; p<0.001) (Table 3).

 

Familial stress scores did not differ significantly at baseline (p=0.783). Both groups demonstrated progressive improvement during follow-up. Statistically significant inter-group differences were observed from the second follow-up onward, with participants receiving pharmacotherapy plus psychotherapy showing greater reductions in familial stress burden. At the final assessment, familial domain scores were significantly lower in the combined therapy group (27.89 ± 9.02) than in the pharmacotherapy group (32.45 ± 7.62; p<0.001) (Table 4).Baseline interpersonal domain scores were comparable between the two groups (p=0.503). Significant within-group improvements were observed across all follow-up visits (p<0.001). Although the combined therapy group consistently demonstrated lower interpersonal stress scores during later follow-ups, inter-group differences did not reach statistical significance at most assessment points, including the final follow-up (p=0.104) (Table 5).Mood and thought domain scores were similar at baseline (p=0.085). Both groups experienced significant reductions during follow-up. Participants receiving combined therapy demonstrated earlier improvement and significantly greater reductions during the seventh and eighth follow-up visits. At the final assessment, mood and thought scores decreased to 39.37 ± 7.34 in the pharmacotherapy group and 31.63 ± 8.60 in the combined therapy group (p<0.001) (Table 6).Baseline personal domain scores were significantly higher in the combined therapy group than in the pharmacotherapy group (65.12 ± 8.19 vs. 61.53 ± 8.86; p=0.038). Both groups showed significant improvement throughout follow-up. However, greater reductions were observed in the combined therapy group during the later follow-up visits. At follow-up eight, personal domain scores were significantly lower in the combined therapy group (20.69 ± 8.46) compared with the pharmacotherapy group (26.50 ± 7.13; p<0.001) (Table 7).Physical health domain scores were significantly higher in the pharmacotherapy group at baseline (64.72 ± 9.55 vs. 59.37 ± 10.52; p=0.009). Significant improvement occurred in both groups throughout follow-up. Participants receiving combined therapy experienced greater reductions during later assessments, resulting in significantly lower physical health stress scores at the eighth follow-up (15.16 ± 8.29 vs. 20.51 ± 8.18; p<0.001) (Table 8).

 

Baseline social domain scores were comparable between treatment groups (p=0.214). Both groups demonstrated significant reductions across all follow-up visits. Inter-group differences became statistically significant from the sixth follow-up onward, with the combined therapy group achieving greater improvement in social functioning. At the final assessment, mean social domain scores were 19.58 ± 8.40 in the combined therapy group compared with 25.36 ± 8.21 in the pharmacotherapy group (p<0.001) (Table 9).Stress-coping domain scores were comparable at baseline (p=0.203). Significant improvement was observed in both treatment groups during follow-up. From the third follow-up onward, participants receiving pharmacotherapy combined with dimension-based psychotherapy demonstrated significantly greater improvement in stress-coping ability than those receiving pharmacotherapy alone. By the eighth follow-up, stress-coping scores had decreased from 71.86 ± 9.44 to 24.76 ± 8.52 in the combined therapy group, compared with a reduction from 69.44 ± 9.12 to 33.09 ± 8.16 in the pharmacotherapy group (p<0.001) (Table 10, Figure 4).

 

RESULTS

Table 1. Inter-group and Intra-group Comparison of Cumulative Stress Load (CSL) Across Follow-ups

Time point

Pharmacotherapy (n = 38) Mean ± SD

Pharma + Psychotherapy (n = 37) Mean ± SD

Inter-group p-value

Intra-group p-value (Pharma vs BL)

Intra-group p-value (Pharma+Psy vs BL)

Statistical Test

CSL_BL

215.52 ± 38.91

212.08 ± 36.44

0.653

Independent t-test

CSL_FU1

191.88 ± 36.47

185.44 ± 34.96

0.371

<0.001

<0.001

Paired t-test

CSL_FU2

176.62 ± 35.82

163.68 ± 31.41

0.058

<0.001

<0.001

CSL_FU3

165.94 ± 34.89

142.06 ± 28.56

<0.001

<0.001

<0.001

CSL_FU4

154.18 ± 32.41

123.72 ± 26.04

<0.001

<0.001

<0.001

CSL_FU5

143.86 ± 30.77

108.92 ± 24.13

<0.001

<0.001

<0.001

CSL_FU6

132.94 ± 28.96

91.24 ± 21.85

<0.001

<0.001

<0.001

CSL_FU7

121.48 ± 27.38

74.88 ± 19.42

<0.001

<0.001

<0.001

CSL_FU8

110.36 ± 25.64

59.72 ± 17.83

<0.001

<0.001

<0.001

 

Figure 1 Inter-group and Intra-group Comparison of Cumulative Stress Load (CSL) Across Follow-ups

 

Table 2. Comparison of Behavioural (B) Domain Scores Across Follow-ups

Time point

Pharmacotherapy (n = 38) Mean ± SD

Pharma + Psychotherapy (n = 37) Mean ± SD

Inter-group p-value

Intra-group p-value (Pharma vs BL)

Intra-group p-value (Pharma+Psy vs BL)

Statistical Test

B_BL

38.04 ± 10.11

36.50 ± 9.26

0.429

Independent t-test

B_FU1

28.01 ± 8.75

31.18 ± 11.40

0.123

<0.001

0.014

Paired t-test

B_FU2

23.39 ± 10.29

23.01 ± 9.42

0.090

<0.001

<0.001

B_FU3

15.92 ± 9.72

15.49 ± 9.65

0.028

<0.001

<0.001

B_FU4

14.20 ± 8.45

14.54 ± 8.55

0.001

<0.001

<0.001

B_FU5

12.66 ± 7.83

12.94 ± 7.64

<0.001

<0.001

<0.001

B_FU6

11.25 ± 7.67

10.45 ± 7.37

<0.001

<0.001

<0.001

B_FU7

9.86 ± 7.42

8.26 ± 6.68

<0.001

<0.001

<0.001

B_FU8

8.52 ± 7.05

6.28 ± 6.05

<0.001

<0.001

<0.001

 

Figure 2. Comparison of Behavioural (B) Domain Scores Across Follow-ups

 

Table 3. Comparison of Emotional Distress (ED) Domain Scores Across Follow-ups

Time point

Pharmacotherapy (n = 38) Mean ± SD

Pharma + Psychotherapy (n = 37) Mean ± SD

Inter-group p-value

Intra-group p-value (Pharma vs BL)

Intra-group p-value (Pharma+Psy vs BL)

Statistical Test

ED_BL

45.51 ± 10.24

43.25 ± 10.57

0.280

Independent t-test

ED_FU1

38.62 ± 11.73

39.73 ± 10.13

0.615

0.007

0.080

Paired t-test

ED_FU2

36.02 ± 9.33

34.67 ± 10.16

0.489

<0.001

<0.001

ED_FU3

29.85 ± 8.86

31.12 ± 9.13

0.482

<0.001

<0.001

ED_FU4

26.30 ± 7.88

27.45 ± 8.20

0.477

<0.001

<0.001

ED_FU5

23.84 ± 7.47

24.50 ± 7.62

0.662

<0.001

<0.001

ED_FU6

21.99 ± 7.57

21.25 ± 7.78

0.631

<0.001

<0.001

ED_FU7

20.13 ± 7.61

18.34 ± 7.69

0.048

<0.001

<0.001

ED_FU8

18.27 ± 7.62

15.18 ± 7.80

<0.001

<0.001

<0.001

 

Table 4. Inter-group and Intra-group Comparison of Familial (F) Domain Scores Across Follow-ups

Time point

Pharmacotherapy (n = 38) Mean ± SD

Pharma + Psychotherapy (n = 37) Mean ± SD

Inter-group p-value

Intra-group p-value (Pharma vs BL)

Intra-group p-value (Pharma+Psy vs BL)

Statistical Test

F_BL

72.05 ± 9.73

72.61 ± 10.41

0.783

Independent t-test

F_FU1

70.34 ± 8.32

67.95 ± 9.46

0.182

0.278

0.032

Paired t-test

F_FU2

64.40 ± 10.52

59.28 ± 8.42

0.008

<0.001

<0.001

F_FU3

51.61 ± 9.01

55.19 ± 10.10

<0.001

<0.001

<0.001

F_FU4

45.49 ± 7.77

49.16 ± 8.67

<0.001

<0.001

<0.001

F_FU5

41.12 ± 7.37

44.31 ± 8.33

<0.001

<0.001

<0.001

F_FU6

38.23 ± 7.45

38.93 ± 8.69

<0.001

<0.001

<0.001

F_FU7

35.39 ± 7.43

33.34 ± 8.89

<0.001

<0.001

<0.001

F_FU8

32.45 ± 7.62

27.89 ± 9.02

<0.001

<0.001

<0.001

 

Table 5. Comparison of Interpersonal (IP) Domain Scores Across Follow-ups

Time point

Pharmacotherapy (n = 38) Mean ± SD

Pharma + Psychotherapy (n = 37) Mean ± SD

Inter-group p-value

Intra-group p-value (Pharma vs BL)

Intra-group p-value (Pharma+Psy vs BL)

Statistical Test

IP_BL

40.65 ± 9.51

39.33 ± 10.19

0.503

Independent t-test

IP_FU1

29.42 ± 10.20

29.35 ± 9.05

0.971

<0.001

<0.001

Paired t-test

IP_FU2

22.02 ± 9.64

25.78 ± 9.72

0.055

<0.001

<0.001

IP_FU3

20.73 ± 9.53

22.10 ± 8.68

0.456

<0.001

<0.001

IP_FU4

18.57 ± 8.40

19.51 ± 7.86

0.569

<0.001

<0.001

IP_FU5

16.58 ± 7.97

17.89 ± 7.62

0.401

<0.001

<0.001

IP_FU6

15.01 ± 7.81

15.11 ± 7.39

0.948

<0.001

<0.001

IP_FU7

13.45 ± 7.67

12.30 ± 7.18

0.441

<0.001

<0.001

IP_FU8

11.94 ± 7.61

9.54 ± 7.01

0.104

<0.001

<0.001

 

Table 6. Comparison of Mood & Thought (M&T) Domain Scores Across Follow-ups

Time point

Pharmacotherapy (n = 38) Mean ± SD

Pharma + Psychotherapy (n = 37) Mean ± SD

Inter-group p-value

Intra-group p-value (Pharma vs BL)

Intra-group p-value (Pharma+Psy vs BL)

Statistical Test

M&T_BL

76.86 ± 9.33

80.13 ± 9.49

0.085

Independent t-test

M&T_FU1

74.36 ± 9.95

72.07 ± 7.94

0.205

0.247

<0.001

Paired t-test

M&T_FU2

67.79 ± 9.67

67.55 ± 11.04

0.909

<0.001

<0.001

M&T_FU3

62.22 ± 8.97

63.05 ± 9.43

0.651

<0.001

<0.001

M&T_FU4

54.46 ± 8.14

55.55 ± 8.76

0.520

<0.001

<0.001

M&T_FU5

48.81 ± 7.28

49.74 ± 8.22

0.550

<0.001

<0.001

M&T_FU6

45.70 ± 7.41

43.92 ± 8.33

0.260

<0.001

<0.001

M&T_FU7

42.49 ± 7.35

37.80 ± 8.57

<0.001

<0.001

<0.001

M&T_FU8

39.37 ± 7.34

31.63 ± 8.60

<0.001

<0.001

<0.001

 

Figure 3 Comparison of Mood & Thought (M&T) Domain Scores Across Follow-ups

 

Table 7. Comparison of Personal Domain Scores Across Follow-ups

Time point

Pharmacotherapy (n = 38) Mean ± SD

Pharma + Psychotherapy (n = 37) Mean ± SD

Inter-group p-value

Intra-group p-value (Pharma vs BL)

Intra-group p-value (Pharma+Psy vs BL)

Statistical Test

P_BL

61.53 ± 8.86

65.12 ± 8.19

0.038

Independent t-test

P_FU1

57.67 ± 8.47

58.31 ± 10.79

0.740

0.019

<0.001

Paired t-test

P_FU2

52.77 ± 9.24

51.44 ± 11.28

0.523

<0.001

<0.001

P_FU3

42.42 ± 8.51

45.04 ± 10.51

0.173

<0.001

<0.001

P_FU4

37.65 ± 7.49

39.40 ± 9.54

0.310

<0.001

<0.001

P_FU5

33.95 ± 6.98

35.62 ± 8.82

0.299

<0.001

<0.001

P_FU6

31.44 ± 7.04

30.57 ± 8.94

0.588

<0.001

<0.001

P_FU7

28.99 ± 7.06

25.66 ± 8.77

<0.001

<0.001

<0.001

P_FU8

26.50 ± 7.13

20.69 ± 8.46

<0.001

<0.001

<0.001

 

Table 8. Comparison of Physical Health (PHY) Domain Scores Across Follow-ups

Time point

Pharmacotherapy (n = 38) Mean ± SD

Pharma + Psychotherapy (n = 37) Mean ± SD

Inter-group p-value

Intra-group p-value (Pharma vs BL)

Intra-group p-value (Pharma+Psy vs BL)

Statistical Test

PHY_BL

64.72 ± 9.55

59.37 ± 10.52

0.009

Independent t-test

PHY_FU1

56.18 ± 9.04

55.87 ± 11.36

0.006

<0.001

0.150

Paired t-test

PHY_FU2

47.28 ± 10.36

43.30 ± 10.72

<0.001

<0.001

<0.001

PHY_FU3

34.68 ± 10.73

35.30 ± 10.07

<0.001

<0.001

<0.001

PHY_FU4

30.92 ± 9.97

31.34 ± 9.07

<0.001

<0.001

<0.001

PHY_FU5

28.35 ± 8.40

28.18 ± 8.53

<0.001

<0.001

<0.001

PHY_FU6

25.81 ± 8.36

23.86 ± 8.32

<0.001

<0.001

<0.001

PHY_FU7

23.09 ± 8.14

19.42 ± 8.32

<0.001

<0.001

<0.001

PHY_FU8

20.51 ± 8.18

15.16 ± 8.29

<0.001

<0.001

<0.001

 

Table 9. Comparison of Social (S) Domain Scores Across Follow-ups

Time point

Pharmacotherapy (n = 38) Mean ± SD

Pharma + Psychotherapy (n = 37) Mean ± SD

Inter-group p-value

Intra-group p-value (Pharma vs BL)

Intra-group p-value (Pharma+Psy vs BL)

Statistical Test

S_BL

58.84 ± 9.68

61.27 ± 10.01

0.214

Independent t-test

S_FU1

54.39 ± 9.54

55.63 ± 9.77

0.521

0.006

<0.001

Paired t-test

S_FU2

48.21 ± 9.63

47.30 ± 9.84

0.645

<0.001

<0.001

S_FU3

42.06 ± 9.41

41.57 ± 9.69

0.796

<0.001

<0.001

S_FU4

38.29 ± 8.72

37.18 ± 8.94

0.537

<0.001

<0.001

S_FU5

34.90 ± 8.41

33.01 ± 8.62

0.259

<0.001

<0.001

S_FU6

31.63 ± 8.35

28.46 ± 8.50

<0.001

<0.001

<0.001

S_FU7

28.42 ± 8.26

24.01 ± 8.33

<0.001

<0.001

<0.001

S_FU8

25.36 ± 8.21

19.58 ± 8.40

<0.001

<0.001

<0.001

 

Table 10. Comparison of Stress Coping (SC) Domain Scores Across Follow-ups

Time point

Pharmacotherapy (n = 38) Mean ± SD

Pharma + Psychotherapy (n = 37) Mean ± SD

Inter-group p-value

Intra-group p-value (Pharma vs BL)

Intra-group p-value (Pharma+Psy vs BL)

Statistical Test

SC_BL

69.44 ± 9.12

71.86 ± 9.44

0.203

Independent t-test

SC_FU1

64.83 ± 8.77

63.12 ± 8.69

0.318

0.004

<0.001

Paired t-test

SC_FU2

58.21 ± 9.03

55.47 ± 9.26

0.128

<0.001

<0.001

SC_FU3

52.44 ± 8.71

49.03 ± 8.95

0.041

<0.001

<0.001

SC_FU4

47.69 ± 8.49

43.52 ± 8.73

0.015

<0.001

<0.001

SC_FU5

43.31 ± 8.26

38.94 ± 8.61

0.011

<0.001

<0.001

SC_FU6

39.88 ± 8.24

34.01 ± 8.39

<0.001

<0.001

<0.001

SC_FU7

36.45 ± 8.21

29.18 ± 8.47

<0.001

<0.001

<0.001

SC_FU8

33.09 ± 8.16

24.76 ± 8.52

<0.001

<0.001

<0.001

 

Figure 4 Comparison of Stress Coping (SC) Domain Scores Across Follow-ups

 

DISCUSSION

The present study demonstrated a significant reduction in cumulative stress load in both treatment groups; however, participants receiving pharmacotherapy combined with dimension-based psychotherapy showed significantly greater improvement from the third follow-up onward. Mean CSL decreased from 212.08 ± 36.44 to 59.72 ± 17.83 in the combined therapy group compared with 215.52 ± 38.91 to 110.36 ± 25.64 in the pharmacotherapy-alone group (p<0.001). These findings are consistent with Bahlmann et al. (2022) [14], who reported that the Relapse Prevention Intervention after Suicidal Event (RISE) improved psychological stabilization and relapse prevention in patients following suicide attempts, supporting the benefit of adjunctive psychotherapy.Behavioural stress scores improved significantly in both groups, with greater reduction in the combined therapy group (from 36.50 ± 9.26 to 6.28 ± 6.05) than in the pharmacotherapy group (from 38.04 ± 10.11 to 8.52 ± 7.05; p<0.001). Similar findings were reported by Bahlmann et al. (2022) [14], who observed improvements in behavioural regulation and reduced recurrence of suicidal crises following structured psychotherapy.Both groups showed significant reductions in emotional distress, with the combined therapy group achieving lower scores at the final follow-up (15.18 ± 7.80) than the pharmacotherapy group (18.27 ± 7.62; p<0.001). These findings agree with Aigner et al. (2006) [15], who demonstrated that reductions in depressive symptoms were accompanied by improved quality of life and psychosocial functioning.Familial stress decreased significantly in both groups, with greater improvement in the combined therapy group (27.89 ± 9.02) compared with the pharmacotherapy group (32.45 ± 7.62; p<0.001). Aschan et al. (2013) [16] reported that adverse family circumstances and socioeconomic disadvantage were major contributors to suicidal behaviour, emphasizing the importance of addressing family-related stress during treatment.Interpersonal stress improved significantly in both groups, although inter-group differences were not statistically significant at most follow-up visits. Scores decreased from 39.33 ± 10.19 to 9.54 ± 7.01 in the combined therapy group and from 40.65 ± 9.51 to 11.94 ± 7.61 in the pharmacotherapy group. Aschan et al. (2013) [16] similarly identified interpersonal adversity as an important determinant of suicidal behaviour, suggesting that improvement in interpersonal functioning requires sustained psychosocial intervention.

 

Mood and thought scores improved significantly in both groups, with significantly greater reductions in the combined therapy group by the seventh and eighth follow-ups (31.63 ± 8.60 vs. 39.37 ± 7.34; p<0.001). These findings support the American Psychiatric Association (2010) [17] practice guideline, which recommends integrating cognitive and psychotherapeutic interventions with pharmacotherapy for patients at suicidal risk.Both groups demonstrated significant improvement in personal stress, with greater reductions observed in the combined therapy group (20.69 ± 8.46) than in the pharmacotherapy group (26.50 ± 7.13; p<0.001). Aigner et al. (2006) [15] also reported that improvement in depressive symptomatology was associated with better personal functioning and enhanced quality of life.Physical health-related stress decreased significantly in both groups, with the combined therapy group showing greater improvement (15.16 ± 8.29) than the pharmacotherapy group (20.51 ± 8.18; p<0.001). Similar observations were made by Aigner et al. (2006) [15], who found that reduced depressive symptoms were associated with improvements in physical health and overall well-being.Social stress scores improved progressively in both treatment groups, with significantly greater improvement in the combined therapy group from the sixth follow-up onward. Final scores were 19.58 ± 8.40 in the combined therapy group and 25.36 ± 8.21 in the pharmacotherapy group (p<0.001). Aschan et al. (2013) [16] similarly demonstrated that poor social support and socioeconomic disadvantage were strongly associated with suicidal behaviours.Stress-coping scores improved significantly in both groups, with greater improvement in the combined therapy group. Scores declined from 71.86 ± 9.44 to 24.76 ± 8.52 compared with 69.44 ± 9.12 to 33.09 ± 8.16 in the pharmacotherapy group (p<0.001). These findings are consistent with Bahlmann et al. (2022) [14], who reported enhanced coping skills following structured psychotherapy. Additionally, Bai et al. (2022) [18] highlighted the increasing burden of depression among young individuals, emphasizing the need for interventions that strengthen adaptive coping mechanisms to reduce suicide risk.

 

CONCLUSION

The present study demonstrated that multidimensional stress assessment effectively identified the major stress domains contributing to suicidal risk among young females. Although both treatment approaches significantly reduced cumulative stress burden, pharmacotherapy combined with dimension-based psychotherapy produced earlier, greater, and more sustained improvements across multiple stress domains than pharmacotherapy alone. These findings support the incorporation of individualized stress profiling and targeted psychotherapeutic interventions into the routine management of young females with suicidal risk.

 

Limitation of the Study

The study was conducted at a single tertiary care center with a relatively small sample size, which may limit the generalizability of the findings. Additionally, the follow-up period was relatively short, precluding assessment of the long-term sustainability of treatment effects and recurrence of suicidal behaviour.

 

REFERENCES

  1. World Health Organization. Suicide: Fact sheet. Geneva: World Health Organization; 2025.
  2. World Health Organization. Suicide worldwide in 2021: Global health estimates. Geneva: World Health Organization; 2024.
  3. Bridge JA, Goldstein TR, Brent DA. Adolescent suicide and suicidal behaviour. J Child Psychol Psychiatry. 2006;47(3-4):372–94.
  4. Hawton K, Saunders KEA, O'Connor RC. Self-harm and suicide in adolescents. Lancet. 2012;379(9834):2373–82.
  5. Carretta RF, et al. Gender differences in risks of suicide and suicidal behaviours: A literature review. Harv Rev Psychiatry. 2024;32(4):209–23.
  6. Turecki G, Brent DA. Suicide and suicidal behaviour. Lancet. 2016;387(10024):1227–39.
  7. O'Connor RC, Kirtley OJ. The integrated motivational-volitional model of suicidal behaviour. Philos Trans R Soc Lond B Biol Sci. 2018;373(1754):20170268.
  8. Franklin JC, Ribeiro JD, Fox KR, Bentley KH, Kleiman EM, Huang X, et al. Risk factors for suicidal thoughts and behaviours: A meta-analysis of 50 years of research. Psychol Bull. 2017;143(2):187–232.
  9. Chamarro A, et al. Stress and suicide risk among adolescents: The role of emotional regulation and behavioural factors. BMC Public Health. 2024;24:1128.
  10. Aschan L, Goodwin L, Cross S, Moran P, Hotopf M, Hatch SL. Suicidal behaviours in South East London: Prevalence, risk factors and the role of socio-economic status. J Affect Disord. 2013;150(2):441–9.
  11. Nock MK, Borges G, Bromet EJ, Alonso J, Angermeyer M, Beautrais A, et al. Cross-national prevalence and risk factors for suicidal ideation, plans and attempts. Br J Psychiatry. 2008;192(2):98–105.
  12. Ahmed F, et al. Suicide and self-harming among young women: A multidimensional analysis. Healthcare (Basel). 2025;13(11):1284.
  13. Franklin JC, Ribeiro JD, Fox KR, Bentley KH, Kleiman EM, Huang X, et al. Risk factors for suicidal thoughts and behaviours: A meta-analysis of 50 years of research. Psychol Bull. 2017;143(2):187–232.
  14. Bahlmann L, Lübbert MBJS, Sobanski T, Kastner UW, Walter M, Smesny S, et al. Relapse Prevention Intervention after Suicidal Event (RISE): feasibility study of a psychotherapeutic short-term program for inpatients after a recent suicide attempt. Front Psychiatry. 2022;13:937527.
  15. Aigner M, Förster-Streffleur S, Prause W, Freidl M, Weiss M, Bach M. What does the WHOQOL-BREF measure? Measurement overlap between quality of life and depressive symptomatology in chronic somatoform pain disorder. Soc Psychiatry Psychiatr Epidemiol. 2006;41(1):81-86.
  16. Aschan L, Goodwin L, Cross S, Moran P, Hotopf M, Hatch SL. Suicidal behaviours in South East London: prevalence, risk factors and the role of socio-economic status. J Affect Disord. 2013;150(2):441-449.
  17. American Psychiatric Association. Practice guideline for the assessment and treatment of patients with suicidal behaviours. Arlington (VA): American Psychiatric Association; 2010.
  18. Bai R, Dong W, Peng Q, Bai Z. Trends in depression incidence in China, 1990-2019. J Affect Disord. 2022;296:291-297.
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