Startseite Effect of self-hypnosis on fear and pain of natural childbirth: a randomized controlled trial
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Effect of self-hypnosis on fear and pain of natural childbirth: a randomized controlled trial

  • Batool Kamalimanesh ORCID logo , Maryam Moradi ORCID logo EMAIL logo , Mehdi Fathi ORCID logo , Maliheh Afiat ORCID logo , Mahnaz Boroumand Rezazadeh ORCID logo und Mohammad Taghi Shakeri ORCID logo
Veröffentlicht/Copyright: 26. Februar 2025

Abstract

Objectives

A clinical trial was conducted to address the trend of high cesarean section rates resulting from maternal fear of childbirth. This trial aimed to investigate the effectiveness of self-hypnosis in mitigating fear and pain during childbirth.

Methods

This study was a parallel, not blinded, randomized controlled trial conducted in 2019 in Mashhad, Iran. Ninety-three nulliparous women were selected by convenience sampling and randomized by random allocation software (4 blocking groups) to either self-hypnosis or control groups. During the clinical trial, both groups received usual care for pregnancy and childbirth. However, the self-hypnosis group also participated in two hypnosis sessions and was given two audio files to practice self-hypnosis at home until delivery. The follow-up period ranged from the 37th week of pregnancy to the postpartum period. Fear of childbirth was assessed at 39 weeks and at cervical dilatation of 8–10 cm, while labor pain was measured at the same stage of labor as the primary outcomes between two groups. Data were analyzed using SPSS 16, applying the Independent sample t-test, Mann–Whitney U test, and Chi-square test. A p-value of less than 0.05 was considered statistically significant.

Results

Thirty women in the self-hypnosis group, aged 24.96±5.42, and 33 women in the control group, aged 23.63±4.68, completed the study. The average scores of fear of childbirth during pregnancy at 39 weeks (self-hypnosis: 46.46±14.53, control: 73.18±17.91), during the active phase of labor at cervical dilatation of 8–10 cm (self-hypnosis: 40.80±17.37, control: 75.12±19.40), and labor pain at cervical dilatation of 8–10 cm (self-hypnosis: 83.03±16.43, control: 95.36±10.36) were significantly lower in the self-hypnosis group compared to the control group (p<0.001 for all).

Conclusions

Our findings suggest that self-hypnosis could be a more effective intervention than usual care alone for reducing fear and pain during natural childbirth in nulliparous women.

Background

The fear and anxiety a mother may experience as childbirth approaches is known as the “fear of childbirth” (FOC). FOC prevalence varies by country due to differences in the definition of concepts, FOC measurement time, and cultural diversity [1]. In European countries, the overall rate of FOC was 1.9–14 % [2], with moderate and severe FOC rates reported to be 19.6 and 6.1 % respectively in Iran [3]. FOC can be particularly prevalent in women who have not previously given birth. The most common causes contributing to this anxiety are fear of labor pain and the baby’s health [1]. Fear can lead to increased catecholamine release during labor, resulting in a cycle of fear-tension-pain [4]. Among the side effects of this cycle are severe labor pain, dystocia, and prolonged labor [5].

In Iran, many women choose cesarean sections due to FOC, leading to a high rate of C-sections (48 %, compared to the WHO’s 15 % recommendation) [6], 7]. This can result in maternal complications such as infection and bleeding, as well as fetal issues like low APGAR scores [8], 9]. To address this, natural childbirth promotion programs, including pain relief methods, have been introduced in Iranian maternity hospitals since 2014 [10], 11]. Epidural analgesia is the most effective pain relief method during labor. However, patient preferences, contraindications, limited availability, and technical issues may necessitate the use of alternative methods. These alternatives include systemic pharmacologic agents, typically administered by inhalation (like nitrous oxide) or injection, and nonpharmacologic approaches such as yoga, music therapy, massage, reflexology, shiatsu, acupuncture, birthing balls, transcutaneous electrical nerve stimulation, and hypnosis [12].

Hypnosis is a state of focused attention and reduced peripheral awareness that enhances one’s responsiveness to suggestions [13]. Hypnosis is affordable, safe, effective, and it does not require any special equipment. It can be used with various patient groups and in different clinical settings. Its therapeutic benefits, particularly in anesthesia, can typically be experienced within minutes or even seconds. Additionally, hypnosis can be practiced independently through self-hypnosis, offering further convenience and accessibility [14].

Despite being considered a benign process, certain studies have identified potential side effects such as headache, dizziness, nausea, anxiety, or panic. These complications can vary in intensity and duration and are classified as short-term or long-term complications. Ambivalence, which is a conflict between the desire to be hypnotized and the anxiety or wish not to be, may result in a headache, as suggested by Hilgard (1974) [15].

To understand how someone responds to hypnosis, it’s important to consider personal risk factors like unmet sexual or social needs, alcohol or drug addiction, and personal biases. Professional risk factors, inadequate knowledge, training, and skills, also play a role. The environment or research settings can significantly impact an individual’s experience with hypnosis [15]. To assess an individual’s hypnotic ability, a range of tests, like the Hypnotic Induction Profile, and the Elkins Hypnotizability Scale can be employed [16], 17].

Hypnosis is an effective tool in obstetrics, helping manage conditions like nausea, labor pain, hypertension, and preterm labor [18]. Self-hypnosis during childbirth empowers women to control anxiety and stress levels [19]. According to previous research by Downe et al. (2015), hypnosis is characterized by a decrease in the experience of FOC in the two weeks following delivery. Moreover, to the best of our knowledge, no studies have investigated the effect of hypnosis or self-hypnosis on FOC during pregnancy and labor. So, this study sought to explore the potential benefits of self-hypnosis in managing these issues.

Methods

This study was a parallel, not blinded, randomized controlled trial conducted in 2019 in Mashhad, Iran. In this study, participants were randomly assigned to two groups: the intervention and the control groups. The intervention group received usual care along with self-hypnosis training, while the control group received usual care. It is worth noting that neither the researchers nor the participants were blinded in this research design.

Ethical considerations

This study was a midwifery dissertation for a M.Sc. degree that was sanctioned by the Mashhad University of Medical Sciences in Iran with the code 971166. The study was also approved by the Iran National Committee for Ethics in Biomedical Research (Ethical code: IR.MUMS.NURSE.REC.1398.005) and was registered in the Iran Registry of Clinical Trials. Written informed consent was obtained from all participants.

Measures

The researchers utilized various data collection tools, as follows:

Demographic survey questions (DSQ)

The researcher created a paper with three sections to gather demographic, pregnancy, and labor information, essential for understanding participants’ backgrounds and experiences during childbirth.

Hypnotic induction profile (HIP)

This scale evaluates the up gaze and eye roll, are graded from zero to four degrees according to the observation of the amount of visible sclera between the lower eyelid and the cornea; a score of zero indicates no hypnotizability, a score of 1 indicates mild, a score of 2 indicates moderate, a score of 3 indicates good and a score of 4 indicates excellent hypnotisability [16]. The reliability coefficient of the HIP was r: 0.805 in this study and was measured at 35/0–36/6th gestational week/day as inclusion criteria.

The depression, anxiety, stress scale-21 (DASS-21)

This scale consists of 21 Likert-scale items, which are grouped into subscales for stress, anxiety, and depression. The cutoff points for high total score, severe depression, severe anxiety, and severe stress were greater than 60, 21, 15, and 26, respectively. The DASS-21 Persian version was confirmed to be valid and reliable by Sahebi et al. (2005), with alpha coefficients of 0.90, 0.91, and 0.84 for the stress, depression, and anxiety subscales, respectively [20]. In this study, stress, anxiety, and depression at 35/0–36/6th gestational week/day were measured as inclusion criteria.

The Wijma delivery expectancy/experience questionnaire version A (W-DEQ (A))

The W-DEQ (A) is a 33-question survey that uses a 6-point Likert scale. The scores range from zero to 165, (0–37 mild, 38–65 moderate, 66–84 severe). The cutoff score for clinical fear is 85 or above [21]. The Persian version of the questionnaire (version A) was validated and shown to be reliable in Iran, with a Cronbach’s alpha coefficient of 0.914 [22]. It is important to keep in mind that the W-DEQ (A) measures FOC during pregnancy. In this study, the W-DEQ (A) measured FOC at 35/0–36/6th gestational week/day as an inclusion criterion and at 39/0th gestational week/day as a primary outcome.

The delivery fear scale (DFS)

The DFS was designed by Wijma et al. in 2002 and was subsequently translated and validated by Saeedi et al. in Iran in 2019. The scale measures FOC during labor and consists of 10 items, with each item being scored between 1 and 10. A score of 1 indicates that the respondent does not agree with the statement at all, while a score of 10 indicates complete agreement. The highest and lowest levels of fear are scored at 100 and 10, respectively. Saeedi et al. measured the reliability of the Persian version of the scale using Cronbach’s alpha, which was found to be 0.80 [23], 24]. In this study, FOC was measured at 4–5 cm and 8–10 cm of cervical dilatation as secondary and primary outcomes, respectively.

The numerical rating scale (NRS)

This scale measures pain levels on a horizontal line from zero to 100 mm, with zero representing no pain and 100 representing unbearable pain. Scores are categorized as mild (0–39), moderate (40–79), or severe (80–100) [25]. The reliability of the NRS was 0.83 in this study. In this study, labor pain was measured at 4–5 cm and 8–10 cm cervical dilatations as secondary and primary outcomes, respectively.

Participants

A clinical trial at Umm Al-Banin Hospital in Mashhad, Iran involved 93 nulliparous women. They were recruited in two ways: through phone calls to those attending childbirth classes and by inviting those visiting the pregnancy clinic. Recruitment took place from May to October 2019, with follow-up until December 2019. Following this, a checklist of inclusion criteria and written consent were obtained from all women at 35/0–36/6th gestational week/day. Those who fulfilled all inclusion criteria were randomly assigned to the self-hypnosis or control groups.

Inclusion criteria

Iranian nationality, 18–35 years old, nulliparous, 35/0–36/6th gestational week/day, carrying a single, healthy fetus with low-risk pregnancy, no addiction to drugs, alcohol or psychotropic medicines, no indication of CS, the intention to have a natural birth at the research hospital, no severe depression, anxiety or stress based on the DASS-21, having medium to very high hypnotizability according to the HIP, and having medium or severe FOC according to the W-DEQ (A).

Withdrawal criteria

Unwillingness to continue, receiving outside counseling on the study topic, adverse events for the mothers, missed hypnosis sessions, listening to audio files less than 10 times per week, inability to perform self-hypnosis, high-risk pregnancy and labor, failure to go to the research hospital for childbirth, CS, and receiving pain killers (spinal, epidural, Entonox, and narcotics).

Interventions

The control group received standard pregnancy and childbirth care. The self-hypnosis group attended two 60–90 minute hypnosis training sessions at 37/0th and 38/0th weeks/day, in addition to usual care. They also listened to two audio files twice a day until delivery. Self-hypnosis ability was assessed at 39/0 weeks/day, and those unable to perform it were excluded.

Usual care

Pregnancy and childbirth care in Iran followed strict protocols, including weekly prenatal care and birth preparation education by midwives and obstetricians. Mothers were admitted for labor only if they showed true signs and had access to pain relief facilities. Cesarean sections were performed only when necessary, and mothers and infants were discharged within 24 hours if there were no complications.

Self-hypnosis intervention

Audio files

Seven participants were interviewed to determine the causes of their FOC and their attitudes toward it. Based on the interviews, two self-hypnosis audio files with different condition keys were designed and approved by the head of the Asian Hypnosis Association. The audio files were then provided to the seven women who participated in the interviews, all of whom were able to successfully engage in self-hypnosis.

First hypnosis session

The first session, which was held at 37/0 weeks/day of pregnancy, was scheduled to explain the general information regarding hypnosis, self-hypnosis, and the implementation of the progressive muscle relaxation technique. Furthermore, suggestions and conditioning techniques were used to create a positive mental image of the birthing room, midwives, maternal voices, and contractions. At the end, the mothers were asked to listen to audio file No. 1 (15 min) at home twice a day (morning and evening) until the second session.

Second hypnosis session

In the second session, which was held at 38/0th week/day of pregnancy, the midwife went over the topics that were discussed in the previous session and repeated them for the mothers. She also conducted a conditioning technique aimed at helping the mothers deal with any fear or pain they might experience during vaginal examinations, midwifery interventions, and contractions. Additionally, the midwife made suggestions for the birth and the baby’s age progression to further reduce any fear of delivery and the baby’s health. Towards the end of the session, the mothers were given audio file No. 2 (15 min) to listen to at home twice a day (morning and evening) until delivery. The midwife contacted the mothers twice a week by phone to ensure that they were following through with their practice. Finally, the mothers were instructed to contact the midwife when they went to the hospital for childbirth. Labor could have started spontaneously or been induced by a doctor.

Self-hypnosis during childbirth

During labor, the mothers used self-hypnosis using the suggestion technique. Additionally, whenever they experienced a contraction, they subconsciously placed their right thumb (conditioning key) inside their fist, squeezed it, took deep breaths, and relaxed, all according to the conditioning technique that was induced.

Outcomes

Outcomes included:

  1. Measuring the level of FOC using the W-DEQ (A) questionnaire at the 39/0 weeks/day of gestation

  2. Measuring FOC at 4–5 cm and 8–10 cm of cervical dilatation using the DFS

  3. Measuring labor pain at 4–5 cm and 8–10 cm of cervical dilatation using the NRS

  4. Collecting pregnancy and labor information using the DSQ 2 h after childbirth

Primary outcomes

The study examined FOC at 39/0 weeks/day and FOC and labor pain at 8–10 cm of cervical dilatation as the primary outcomes.

Secondary outcomes

The secondary outcomes included FOC and labor pain at 4–5 cm cervical dilatation, pregnancy age, labor augmentation, postpartum hemorrhage, APGAR score, neonate weight, hospitalization at the neonatal intensive care unit (NICU), and participant satisfaction with self-hypnosis.

Sample size

Upon thorough review of various articles on self-hypnosis, we found that the necessary information for determining sample size was not available. Consequently, we opted to utilize the pilot method for the initial 10 participants, as suggested by the statistician. Considering an alpha coefficient of 0.1 and 90 % power, the sample size was calculated using the mean comparison formula in the two independent groups to compare the FOC at the 39/0 weeks/day of pregnancy and the 8–10 cm of cervical dilatation and labor pain at 8–10 cm of cervical dilatation. After calculation, a sample size of n=32 was determined for labor pain, which was greater than the sample size for FOC. Therefore, a sample size of 40 participants was assigned to each group, accounting for a 25 % attrition rate.

Randomization

The participants were grouped into intervention and control groups using Microsoft Excel software with the block randomization method. This ensured an equal distribution of participants between groups and balanced sample sizes. In this study, a block size of 4 was used.

Implementation

The first author, a registered midwife with a clinical hypnosis certificate from the Society of Clinical Hypnosis of Iran, utilized a scheduled random allocation sequence to assign participants to either the intervention or control group.

Statistical methods

The data was analyzed using SPSS software version 16. Both groups were tested for normal distribution using the Kolmogorov‒Smirnov test. The mean and standard deviation (SD) were used for normally distributed variables, while the frequency and percentage were used for qualitative variables. Independent sample t-test was used for normally distributed quantitative variables, and the Mann‒Whitney U test for non-normal or ordinal variables. The chi-square test was used to compare nominal variables between the study groups. A p-value less than 0.05 was considered to indicate statistical significance.

Results

Ninety-three mothers were enrolled in the study, 30 of whom were excluded (12 from the self-hypnosis group and 18 from the control group), leaving 30 and 33 women in the self-hypnosis and control groups, respectively, who completed the study. Although all women in both groups were able to perform self-hypnosis during childbirth, only one pregnant woman in the self-hypnosis group could not accomplish self-hypnosis during pregnancy (Figure 1).

Figure 1: 
CONSORT flow diagram.
Figure 1:

CONSORT flow diagram.

Baseline data

The study revealed that the self-hypnosis group had a mean age of 24.96 years (SD=5.42), while the control group had a mean age of 23.63 years (SD=4.68). The mean extent of hypnotizability in the self-hypnosis group was 2.96 (SD=0.76), and that in the control group was 2.84 (SD=0.75) (Table 1). Additionally, the FOC at the 35/0–36/6th gestational weeks/day was 63.00 (SD=16.43) in the self-hypnosis group and 63.54 (SD=16.74) in the control group (Table 2).

Table 1:

Comparison of demographic and midwifery information between the self-hypnosis and control groups.

Variables Self-hypnosis group (n=30)
Control group (n=33)
Test results
Mean±SD Mean±SD
Age (years)a 24.96±5.42 23.63±4.68 P=0.301
Pregnancy age when entering the study (days)b 260.97±1.86 261.21±1.93 P=0.611
Duration of marriage (years)b 3.35±3.23 2.83±1.80 P=0.866
Body mass index (kg/m2)a 22.98±3.44 23.19±4.29 P=0.832
Extent of hypnotizabilitya 2.96±0.76 2.84±0.75 P=0.540
Variables Self-hypnosis group (n=30)
Control group (n=33)
Test results
n, % n, %
Education levelb High school 7 (23.3) 13 (39.4) P=0.110
Diploma 12 (40.0) 13 (39.4)
Academic 11 (36.7) 7 (21.2)
Income levelb Low 9 (30.0) 12 (36.4) P=0.727
Moderate 21 (70.0) 20 (60.6)
High 0 (0.0) 1 (3.0)
Residencyc Rental 16 (53.3) 20 (60.6) P=0.717
Personal home 8 (26.7) 6 (18.2)
Parents’ home 6 (20.0) 7 (21.2)
  1. aIndependent t-test; bMann‒Whitney U test; cChi‒square test.

Table 2:

Comparison of the means and standard deviations of fear of childbirth in the self-hypnosis and control groups.

Fear of childbirth Self-hypnosis group (n=30)
Control group (n=33)
Intergroup test results
Mean±SD Mean±SD
FOC at the 35/0–36/6th week of pregnancya 63.00±16.43 63.54±16.74 t=0.130, df=61, p=0.897
FOC at the 39/0th week of pregnancya 46.46±14.53 73.18±17.91 t=6.45, df=61, p<0.001
FOC at the 4–5 cm cervical dilatationa 21.83±8.06 59.09±17.75 t=10.54, df=61, p<0.001
FOC at the 8–10 cm cervical dilatationa 40.80±17.37 75.12±19.40 t=7.367, df=61, p<0.001
  1. FOC, Fear of childbirth; a Independent t test.

Primary outcomes

The study findings demonstrated that the mean FOC at the 39/0th week of gestation was significantly lower (p<0.001) in the self-hypnosis group (mean=46.46, SD=14.53) than in the control group (mean=73.18, SD=17.91) (Table 2).

The results revealed that at 8–10 cm of cervical dilatation, there was a marked difference between the self-hypnosis and the control groups. The average FOC was 40.80 (SD=17.37) and 75.12 (SD=19.40) for the self-hypnosis and control groups, respectively. The independent t-test findings confirmed the notable variation (t(61)=7.367, p<0.001) between the two groups, with the self-hypnosis group reporting considerably lower mean FOC scores (Table 2).

Furthermore, during the same stage of labor, the mean pain scores were 83.03 (SD=16.43) and 95.36 (SD=10.36) for the self-hypnosis and control groups, respectively. The Mann‒Whitney U test results also revealed a significant difference (U= −4.396, p<0.001) in the labor pain scores between the two groups, with the self-hypnosis group having significantly lower scores (Table 3).

Table 3:

Comparison of the mean and standard division of labor pain scores in the self-hypnosis and control groups.

Variables Self-hypnosis group (n=30)
Control group (n=33)
Intergroup test results
Mean±SD Mean±SD
Pain at 4–5 cm cervical dilatationa 54.23±20.29 68.66±17.97 t=2.99, df=61, p<0.004
Pain at 8–10 cm cervical dilatationb 83.03±16.43 95.36±10.36 U= −4.396 p<0.001
  1. aIndependent t test; bMann‒Whitney U test.

Secondary outcomes

Our research has shown that teaching women self-hypnosis during labor and delivery can lead to a lower likelihood of cesarean section. The mean FOC and labor pain scores at 4–5 cm of cervical dilatation are shown in Tables 3 and 4. Notably, there were no significant differences between the self-hypnosis group and the control group in terms of pregnancy duration, labor augmentation, postpartum hemorrhage, APGAR score, neonatal weight, or NICU hospitalization (p>0.05). Table 4 highlights the satisfaction variable, which indicates positive feedback from mothers who learned about self-hypnosis.

Table 4:

Frequency distribution of self-hypnosis satisfaction in the intervention group.

Variable Low
Medium
High
Total
Frequency, % Frequency, % Frequency, % Frequency, %
Satisfaction with self-hypnosis in reducing labor pain 6 (20.0) 13 (43.3) 11 (36.7) 30 (100.0)
Recommending self-hypnosis to others as a method to overcome labor pain 5 (16.7) 10 (33.3) 15 (50.0) 30 (100.0)
Satisfaction with self-hypnosis in reducing fear of childbirth 2 (6.7) 13 (43.3) 15 (50.0) 30 (100.0)
Recommending self-hypnosis to others as a method to overcome fear of childbirth 1 (3.3) 8 (26.7) 21 (70.0) 30 (100.0)

Side effects

The study also evaluated the potential side effects of self-hypnosis by asking mothers about headaches, dizziness, nausea, and anxiety after childbirth. However, no side effects were reported in the self-hypnosis group. In the control group, no specific side effects were observed either.

Discussion

This research aimed to study the impact of self-hypnosis on fear and pain levels in first-time mothers during childbirth. Prior studies have suggested that FOC during pregnancy may lead to fear during labor [26]. Therefore, teaching self-hypnosis during pregnancy could potentially reduce pain and FOC. This study is unique in that it assessed the influence of self-hypnosis on FOC during both pregnancy and labor for the first time.

In this study, we examined the hypnotizability of participants utilizing the “conditioning technique.” Our results demonstrated that conditioning mothers during pregnancy to associate contractions with a specific cue, such as their right thumb, enabled them to enter a hypnotic trance unconsciously during labor, allowing for posthypnotic suggestions without conscious awareness. The absence of a standardized methodology for hypnosis protocols complicates comparisons of different techniques and their effectiveness, which may explain the difference in our findings compared to some prior research, although the majority of literature aligns with our results [27], [28], [29], [30].

It is important to note that only the data analyst was blinded in this study. Previous studies have suggested that hospital staff caring for the self-hypnosis group often misattributed calmness to a lack of labor progress tied to stress among intervention participants [31]. Additionally, research by Werner et al. indicates that blinding physicians, particularly midwives, may interfere with the hypnosis process [32]. Consequently, the other researchers and hospital staff were aware of the participants’ self-hypnosis. To eliminate bias, participants who received pain relief (spinal, epidural, Entonox, and narcotics) were explicitly excluded from the study. In such cases, it was clear that any observed pain reduction could not be attributed to self-hypnosis, but rather to the pain relief methods themselves.

A key strength of this study was the monitoring of participants’ daily self-hypnosis practice, which may have contributed to the reduction in pain at 4–5 and 8–10 cm cervical dilatation. In the study by Beevi et al. (2017), none of the participants in the intervention group requested an epidural [33]. In contrast, Downe et al. (2015) found that only one-third of participants recorded their practice, while Cyna et al. (2013) noted that less than one-third attended all hypnosis sessions, indicating low adherence and limited pain reduction [34], 35]. The results of Werner et al.’s study indicated that hypnotizability was solely evaluated in the self-hypnosis group, and the three groups were not homogeneous in terms of hypnotizability [36]. However, research has demonstrated that the capacity to alleviate pain through hypnosis is significantly influenced by hypnotizability, with highly hypnotizable participants being more capable of reducing pain than their less hypnotizable counterparts under identical circumstances [37]. It should be noted that the hypnosis technique used in Werner et al.’s (2013) study countered the one employed in the present study, as they utilized the suggestion of forgetfulness during labor, which is a challenging hypnosis phenomenon that only 20–25 % of individuals can fully experience [38]. Nevertheless, Werner et al.’s (2013) study was a large randomized trial with a high response rate of nearly 100 % at follow-up, while our study had a smaller sample size.

In our study, we evaluated the severity of labor pain during childbirth. However, two previous studies, namely, Downe et al. (2015) and Cyna et al. (2013), measured this pain at two and six weeks after delivery, respectively [34], 35]. The literature suggests that the severity of pain experienced during labor is not necessarily correlated with either the anticipated pain experienced during pregnancy or the postpartum pain experienced by the mother [26].

Thus, measuring childbirth pain may not represent actual delivery pain. Downe et al.’s (2015) study on self-hypnosis for labor was the largest randomized controlled trial, but the decreased response rate after two weeks may limit the generalizability of their findings.

Excessive anxiety during childbirth can increase catecholamines, particularly epinephrine, leading to muscle spasms, vasoconstriction, visceral injuries, and intensified pain [39]. However, hypnosis can disrupt the connection between the amygdala-limbic system and the cerebral cortex, inhibiting the interpretation of emotions such as fear and pain [40]. In hypnosis, there is a reduction in positive tonus within the cortex, attributed to radiating inhibition. When a word or command from the hypnotist is directed at a specific region of the cortex, it concentrates the excitatory process at that site. This concentration is swiftly followed by negative induction, allowing the effect to propagate across the entire cortex without resistance. Consequently, the directive word or command becomes entirely isolated from external influences, acting as an absolute and compelling stimulus, even after the subject has returned to a waking state [41]. Research shows that hypnosis is a safe method for mitigating pain during labor and postpartum [42], enhancing the likelihood of vaginal birth and reducing the need for cesarean section.

Limitations

  1. It is important to note that the sample size was small; therefore, the results may not be applicable to all pregnant women with different demographic and midwifery characteristics.

  2. We had a higher than expected attrition rate (25 %) due to the lack of communication about childbirth admissions and cesarean sections. The intervention group had a 35.3 % attrition rate, while the control group had 28.6 %. We recruited 42 and 51 participants for the intervention and control groups, respectively, to achieve our goal.

  3. Attitudes toward self-hypnosis may have also impacted the results, although the study attempted to mitigate this through random group division.

Conclusions

Research indicates that self-hypnosis can help reduce the fear of childbirth and labor pain for first-time pregnant women. It can alleviate anxiety and stress, increase self-confidence, and positively impact the well-being of both mothers and fetuses. This cost-effective method shows potential for improving pregnancy outcomes, especially for medium to highly hypnotizable mothers. However, more research is needed to understand its effects on a larger sample of women and how it compares to other pain management techniques during labor.


Corresponding author: Maryam Moradi, Global and Women’s Health, School of Public Health and Preventive Medicine, Faculty of Medicine, Nursing and Health, Monash University, Melbourne, Australia; and Nursing and Midwifery Care Research Center, Mashhad University of Medical Sciences, Mashhad, Iran, E-mail:

Award Identifier / Grant number: 971166

Acknowledgments

The authors express their gratitude towards the Vice Chancellor for Research of the University, who sponsored this project, the professors of the School of Nursing and Midwifery, and the sincere cooperation of the staff of Umm Al-Banin Hospital and the mothers who participated in this study. Their support and participation played a crucial role in the success of this research project.

  1. Research ethics: This study was a midwifery dissertation for a M.Sc. degree that was sanctioned by the Mashhad University of Medical Sciences in Iran with the code 971166. The study was also approved by the Iran National Committee for Ethics in Biomedical Research (Ethical code: IR.MUMS.-NURSE.REC.1398.005) and was registered in the Iran Registry of Clinical Trials (IRCT20190129042538N1).

  2. Informed consent: Written informed consent was obtained from all participants.

  3. Author contributions: The present study is the result of the Midwifery M.Sc. thesis of the first author (B.K.) under the supervision of M.M. B.K., M.M. and M.F. contributed to conceptualization, methodology, review, and editing in writing. B.K., M.A. and M.B.R. collected the samples. B.K. and M.M. drafted the manuscript. M.T.S., B.K. and M.M. have performed statistical analysis. B.K, M.M., M.T.S. and M.F. interpreted the results. All authors critically reviewed and revised the final manuscript.

  4. Use of Large Language Models, AI and Machine Learning Tools: The authors of this manuscript declare that no artificial intelligence (AI) was used during the writing process.

  5. Conflict of interest: The authors have no potential conflicts of interests with respect to the research, authorship, and/or publication of this article.

  6. Research funding: This article is the outcome of a M.Sc. thesis with code 971166, financially supported by the Vice-Chancellor in Research Affairs, Mashhad University of Medical Sciences.

  7. Data availability: The datasets from this study are available from the corresponding author upon reasonable request.

References

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Received: 2024-10-11
Accepted: 2025-01-07
Published Online: 2025-02-26

© 2025 the author(s), published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 International License.

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