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.
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
Exclusion Criteria
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:
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:
The SSDQ domains included:
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
Secondary outcomes
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.
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.
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