Randomized Controlled Trial
Copyright ©The Author(s) 2025.
World J Psychiatry. Sep 19, 2025; 15(9): 109458
Published online Sep 19, 2025. doi: 10.5498/wjp.v15.i9.109458
Table 1 Comparison of general data between two groups of patients, n (%)
Group
n
Age (years)
BMI (kg/m2)
Gender
Smoke
Alcohol
Course of disease (months)
Years of education (years)
Pretherapy HAMD-24
Male
Female
Combined group5633.8 ± 8.124.10 ± 2.1438 (67.86)18 (32.14)31 (55.36)35 (62.50)15.81 ± 8.8011.7 ± 3.041.8 ± 4.3
Control group5434.5 ± 8.923.76 ± 2.3434 (62.96)20 (37.04)28 (51.85)31 (57.41)16.32 ± 8.7312.4 ± 3.440.5 ± 4.1
t/χ2-1.0430.7920.2910.1360.297-1.449-1.1401.615
P value0.2990.4300.5890.7120.5860.1500.2570.109
Table 2 Comparison of electroconvulsive therapy monitoring indicators between combination group and control group

n
Initial threshold charge (mc)
Final threshold charge (mc)
Total treatment electricity (mc)
Mean seizure duration (mc)
Combined group56116.02 ± 13.76144.01 ± 13.731266.07 ± 212.0150.06 ± 8.08
Control group54114.18 ± 14.56170.23 ± 24.761866.02 ± 260.8248.77 ± 8.82
t value2.007-52.149-99.2852.016
P value0.4750.0000.0000.478
Table 3 Comparison of Wisconsin Card Sorting Test scores between the combined group and the control group before and after treatment

n
Total number of answers
Accuracy
Percentage of conceptualization level
Continuous response
Non persistent error
Number of categories completed
Combined group56
    Before treatment129.73 ± 14.970.58 ± 0.150.45 ± 0.2213.42 ± 7.3445.68 ± 14.822.46 ± 1.82
    After treatment108.22 ± 15.11a,b0.68 ± 0.14a,b0.61 ± 0.18a,b7.39 ± 6.78a,b31.23 ± 17.07a,b3.72 ± 2.14a,b
Control group54
    Before treatment129.12 ± 15.280.59 ± 0.140.45 ± 0.2313.97 ± 7.1145.41 ± 15.352.55 ± 2.04
    After treatment114.59 ± 16.84a0.65 ± 0.15a0.58 ± 0.20a8.72 ± 7.14a34.65 ± 18.26a3.47 ± 2.41a
Table 4 Comparison of Tower of Hanoi test results between the combined group and the control group before and after treatment

n
Total score
Average planning time (second)
Average execution time (second)
Combined group56
    Before treatment42.87 ± 15.7116.42 ± 9.5429.76 ± 10.58
    After treatment64.75 ± 10.27a,b8.62 ± 7.41a,b22.79 ± 9.52a,b
Control group54
    Before treatment43.16 ± 16.9815.94 ± 10.0829.41 ± 10.74
    After treatment61.23 ± 17.49a9.76 ± 8.28a24.35 ± 10.66a
Table 5 Comparison of adverse reactions between the combined group and the control group, n (%)
Group
n
Postoperative dysphoria
Confusion of consciousness
Bradycardia
Headache
Muscle soreness
Bauseated
Emesis
Combined group553 (5.45)4 (7.27)1 (1.82)4 (7.27)3 (5.45)5 (9.09)2 (3.64)
Control group545 (9.26)7 (12.96)3 (5.56)6 (11.11)8 (14.81)8 (14.81)5 (9.26)
χ20.5800.9721.0770.4822.6310.8501.434
P value0.4460.3240.2990.4880.1050.3570.231
Table 6 Comparison of long-term efficacy statistics between two groups of patients

n
BRANS
MCCB
HAMD-24
WCST
TOH
Combined group551.49 ± 0.491.16 ± 0.44-0.54 ± 0.370.07 ± 0.021.28 ± 0.65
Control group541.44 ± 0.521.12 ± 0.47-0.52 ± 0.410.06 ± 0.021.25 ± 0.59
t value0.1820.1060.1240.0850.127
P value0.8740.9260.9080.9560.905