The duration of the active phase (4–5 cm to 10 cm dilation) differed significantly among the groups (Hugo < Sanyinjiao, Hugo < control; P=0.002 for both comparisons). The median duration in the Hugo group was 5 h (interquartile range [IQR]: 4.75–6), compared to 6 h (IQR: 5–7) in both the Sanyinjiao and control groups. Post hoc analysis confirmed a significantly shorter duration in the Hugo group compared to the Sanyinjiao (P<0.001) and control groups (P<0.001).
The duration of the expulsion phase (10 cm dilation to delivery) also varied significantly among the groups (P<0.001). The Hugo group showed a median duration of 15 min (IQR: 10–16.25), while the Sanyinjiao and control groups exhibited longer durations of 37.5 min (IQR: 30–60) and 30 min (IQR: 20–60), respectively. Post hoc analysis indicated significantly shorter durations in the Hugo group compared to the control (P<0.001) and Sanyinjiao groups (P<0.001).
Table 3 presents a detailed comparison of childbirth progress indicators among the three study groups during labor.

Variables measured hourly include cervical dilatation (cm), cervical effacement (%), and fetal station (relative to ischial spines, scale -3 to +3). Most variables showed statistically significant differences between groups (P<0.05). Specifically, the Hugo group exhibited significantly greater effacement percentages and more advanced fetal station positions compared to the control group at multiple time points. Cervical dilation progressed faster in the Hugo group from the second hour onward compared to the control group. The Sanyinjiao group generally demonstrated intermediate values between the Hugo and control groups. All measurements are reported as medians with IQR. These findings suggest that TENS application at the Hugo acupoint may accelerate labor progression compared to other groups. Median times to reach 10 cm dilation were 6 h for the Hugo group and 7 h for both the Sanyinjiao and control groups, indicating similar labor progress between the Sanyinjiao and control groups, while the Hugo group showed a slightly shorter duration.
Discussion
The findings of this study demonstrate that applying TENS at the Hugo point significantly reduces the duration of both the active and expulsion phases of labor in nulliparous women. In contrast, its application at the Sanyinjiao point lacks a similar impact.
Aghamohammadi et al. (2011) utilized TENS at both Hugo and Sanyinjiao points simultaneously in nulliparous women. They found a significantly shorter first stage of labor in the TENS group compared to the placebo group, aligning with the findings regarding the Hugo point in this study. However, there are methodological differences between studies, particularly in the timing of intervention and study design. In another study, the pads of the TENS machine were placed in the lumbar and sacral regions. Based on the results, the duration of the first phase of labor was significantly shorter in the TENS group than in the control group, which is in line with the results of the present study conducted among nulliparous women. However, no significant difference was reported between the two groups regarding the duration of the third stage (Shahoei et al., 2017), which is not in line with that of the present study. The reason for the difference may be related to the difference in the method used in these studies and the location of the TENS pads. In Shahoei’s study, the electrodes were placed over the lumbar and sacral regions, whereas in the present study, they were applied to specific acupressure points (Hugo and Sanyinjiao).
Moradi et al. (2022) reported the duration of the first stage of the active phase of labor in nulliparous women, which showed no significant differences among the three groups: The TENS group, the placebo group, and the psychological counseling group. However, there was a significant difference in the duration of the second stage of the active phase, as well as in the total duration of the active phase, among the three groups, which is in line with our findings. An interventional study involving 160 nulliparous women evaluated the effect of TENS at four points (BL19, PC6, B12, and L14) on labor duration. The duration of labor was significantly shorter in all four groups than in the control group, but no statistically significant difference was reported among the four intervention groups (Peng et al., 2010). Other studies reported a significant reduction in the duration of the active phase of labor while using TENS in the Hugo point (Dong et al., 2015; Njogu et al., 2021; Santana et al., 2016).
In the present study, applying TENS at the Hugo acupoint significantly reduced the duration of labor stages compared to the other two groups. However, Rasaeean et al. (1995) reported that TENS did not shorten labor duration. Additionally, there was a gradual decrease in the effectiveness of TENS from dilatation of 1-8 cm. Similarly, a systematic review and meta-analysis demonstrated that while TENS significantly reduced labor pain, it did not affect the duration of labor (Thuvarakan et al., 2020). The results were inconsistent with those of the present study, and this difference may be due to variations in the placement area of the TENS pads, the type of TENS device used, and the frequency and voltage of the TENS device. The usage of either high or low-frequency TENS system parameters explains this finding. These parameters increase β-endorphins and methionine-enkephalin concentration and the production of inhibitory neurotransmitters such as gamma-aminobutyric acid (GABA) and serotonin, but exhibit a reduction in neurotransmitter release (aspartate and glutamate). These natural analgesic substances inhibit the production of catecholamines (Chalermkitpanit et al., 2017).
This study adhered strictly to the principles of controlled trials to ensure accuracy and reliability. Data collection was carefully performed following standardized protocols to ensure the accuracy and reliability of the results. The labor progress checklist used in this study was developed and validated based on the standards set by the Iranian Ministry of Health and Medical Education (2025). However, the study population was limited to nulliparous women. Future research is suggested to include multiparous women to enable comparisons of labor stage durations between nulliparous and multiparous women. This study did not investigate neonatal outcomes after delivery, which should be addressed in future interventional studies.
Conclusion
This study evaluated the effect of TENS at Hugo and Sanyinjiao acupoints on labor progression and duration in nulliparous women. The results showed that TENS, especially at the Hugo point, significantly reduced the duration of the first and second stages of labor and improved cervical dilation, effacement, and fetal descent. However, the findings also revealed that the second stage of labor was longer in the Sanyinjiao group compared to the control group, which may be due to different physiological responses at the Sanyinjiao point or variations in the method of intervention, indicating the need for further investigation. These findings suggest that TENS can be used as a safe, low-cost, and non-invasive method in maternity education and clinical practice to promote normal childbirth. For healthcare managers, supporting such interventions may improve maternal satisfaction and reduce unnecessary cesarean sections. Future studies are recommended to explore other acupoints, TENS parameters, and long-term maternal outcomes.
Ethical Considerations
Compliance with ethical guidelines
This article is a part of a research project and has been approved by the Ethics Committee of Zanjan University of Medical Sciences, Zanjan, Iran (Code: IR.ZUMS.REC.1398.100). All study procedures were in accordance with the protocol of the Regional Ethical Research Committee and the 1964 Declaration of Helsinki. After being informed about the study objectives, written consent was obtained from all women. They were told that their participation was voluntary, confidential, and anonymous, and they had the right to withdraw from the research at any time. This study was registered in the Iranian Registry of Clinical Trials (IRCT) (Code: IRCT20220221054085N1).
Funding
This study was funded by the Scientific Council of Zanjan University of Medical Sciences, Zanjan, Iran (Project code: A-11-1236-1).
Authors' contributions
Conceptualization: Sanaz Fayazi; Study design: Sanaz Fayazi, Mina Abbasi, and Tahereh Shams Ghoreishi; Data acquisition: Masoumeh Amani; Writing the original draft: Sanaz Fayazi and Masoumeh Amani; Data interpretation, review and editing: Mina Abbasi and Tahereh Shams Ghoreishi, Masoumeh Amani, and Sanaz Fayazi.
Conflict of interest
The authors declared no conflict of interest.
Acknowledgments
The authors thank Zanjan University of Medical Sciences, Zanjan, Iran, and the Vice-Chancellor of Research and Technology for their financial support to carry out the study. The authors want to thank the staff for their collaboration and the mothers for their participation.
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