Pain ManagementNCT06999564
Effects of EFT on Postpartum Safety Perception, Anxiety, and Postoperative Pain After Cesarean Section
A study testing EFT in people with Pain Management and Anxiety, run by KTO Karatay University at 1 site in Turkey (Türkiye).
Trial summary
This study is a parallel randomized controlled trial on 60 primiparous women with cesarean section pain, randomly divided into EFT and control groups. The study was approved by KTO Karatay University Faculty of Medicine Ethics Committee. Read more about this study
- Who is it for?
- Ages 18 to 35 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Pain Management, Anxiety
- What is being tested?
- EFT
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 2 Jun 2025to 13 Dec 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 35 years
- Women only
- Healthy volunteers accepted
- Adult
Who may be able to join
- primary school graduate
- primiparous
- planned cesarean section
- Postoperative pain of 4 or more according to VAS.
Who cannot join
- Heart disease
- high blood pressure
- chronic diseases such as diabetes
- history of miscarriage
- placenta previa
- mental illness in the last year
Show all 13Show fewer
- use of psychoactive drugs
- drug addiction
- cigarette smoking
- preeclampsia
- bleeding
- intrauterine death
- premature birth
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Effect of Eft applıed Before Cesarean sectıon on Postpartum feelıngs of Safety, anxıety and postoperatıve paın: RCT
This study is a parallel randomized controlled trial on 60 primiparous women with cesarean section pain, randomly divided into EFT and control groups. The study was approved by KTO Karatay University Faculty of Medicine Ethics Committee. Women will be included in the study according to the following criteria: at least primary school graduate, primiparous, planned cesarean section and 4 or more postoperative pain according to VAS. Women with chronic diseases such as heart disease, high blood pressure and diabetes, history of miscarriage, placenta previa, mental illness in the past year, psychoactive drug use, drug addiction, smoking, and pregnancy complications such as pre-eclampsia, bleeding, intrauterine death and preterm delivery will be excluded. Data collection will start in June 2025 and will be completed in August 2025.
Read the detailed description
Caesarean section is a surgical operation used when vaginal delivery is risky for the mother and fetus and can have both long and short-term effects on maternal and infant health. It is known that caesarean sections do not have a proven positive effect on mother-baby health, but may have negative consequences. After cesarean section, women may experience various problems such as inability to perform activities of daily living, breastfeeding problems, inability to actively take care of the newborn, decreased postpartum comfort, anxiety, depression, insomnia and pain.
Postoperative pain, one of the most common complications of cesarean section, plays an important role in ensuring skin-to-skin contact, establishing mother-baby bonding, initiating breastfeeding, the mother\'s recovery process and maternal-infant health. In addition, women may experience various levels of stress, anxiety and insecurity after cesarean section. Factors such as spousal support, presence of social support resources, attitudes of health personnel, antenatal education about the postpartum period, general well-being of mother and baby, stress, anxiety, depression, mode of delivery, perception of delivery, birth experience, breastfeeding problems, early discharge are factors affecting mothers\' sense of security in the postpartum period. Failure to provide a sense of security after birth increases the risk of anxiety and depression in the following periods. Factors that increase anxiety in women after cesarean section include surgical operation, prolonged transition to oral feeding, late mobilization, risk of infection, delayed mother-infant interaction and milk release.
Early detection of post-cesarean anxiety and postpartum sense of security and taking measures to address these conditions can improve the mother\'s quality of life, reduce anxiety and worry, and contribute to the effective and efficient maintenance of the mother-infant relationship. Reducing postoperative pain is also of great importance in terms of preventing physical complications and chronic pain, relieving depression, improving the quality of life of the individual, providing postpartum comfort and supporting effective breastfeeding. The side effects of pharmacologic methods used to improve postoperative pain and comfort after cesarean section and the inadequacy of these methods have increased the interest in non-pharmacologic approaches. Nonpharmacological techniques include diaphragmatic breathing exercises, Lamaze methods, visualization, meditation, acupuncture, acupressure, reflexology, massage, hypnosis, aromatherapy, prayer therapy, music therapy and EFT. EFT (Emotional Freedom Techniques) envisages pressing and stimulating the meridian crossing points of the organs associated with these emotions in order to improve psychological conditions such as anger, sadness and anxiety. EFT can resolve emotional problems, reduce anxiety levels, make the person feel calmer and think more positively, supporting maternal and fetal health.
A review of the literature shows that mothers have the most problems with pain, breastfeeding and mobilization after cesarean section and need help with these problems; 78% of women who gave birth by cesarean section experience moderate to severe pain, which negatively affects maternal comfort, and mothers who undergo cesarean section experience unbearable pain of different intensities. In the world, anxiety and depression in the postpartum period have increased in the last decade, as Hada et al. (2019) reported in their study. Postpartum depression rates have been reported to be approximately 13% worldwide. Postpartum anxiety and depression are more common in the early postpartum period and in women who gave birth by cesarean section.
EFT has been reported to be effective in many other areas, including the treatment of disorders such as generalized or specific anxiety, morbid fears, depression, posttraumatic stress disorder, chronic pain and addiction. However, so far, no study has examined the effect of EFT on postpartum feelings of safety, anxiety and postoperative pain together. In the light of this information, unlike the studies in the literature, this study will be conducted to examine the effect of EFT applied before cesarean section on postpartum feelings of safety, anxiety and postoperative pain. In this context, anxiety levels, pain intensity and postpartum feelings of safety will be evaluated in the post-cesarean period. Therefore, it is thought that the results obtained from the study will guide future studies and make a significant contribution to the literature.
- Conditions
- Pain Management, Anxiety
- Being tested
- EFT
- Keywords
- caesarean section, anxiety, sense of course
- Medical subject headings
- Agnosia, Anxiety Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
EFTBehavioural
EFT involves the following steps:
- Identification of the problem that is causing the person distress (e.g., fear of childbirth) and scoring or measuring the severity of this problem.
- Tapping with the fingertips on certain points of the face and body, known as correction (i.e., regulation of the energy system), as well as the expression of an emphatic phrase (related to the person\'s problem and self-acceptance).
| Study group | Role | What they receive |
|---|---|---|
| EFT | Experimental | Three sessions of face-to-face EFT will be applied to mothers who will have a planned cesarean section three days before delivery. In order to examine the effect of EFT on women's feelings of security, anxiety and pain levels after childbirth, face-to-face EFT will be applied to mothers in the postpartum period after cesarean section. Receives: Behavioral: EFT |
| CONTROL | No intervention | No application was made to the control group. Following the pre-test application, VAS, SUI and STAI-I-SATAI-II post-test data will be applied before and after cesarean delivery. After the data were reported, EFT was applied to the women in the control group individually by the researchers. |
What is being measured
The primary outcome is the main question the study is designed to answer.
EFT for women who had a planned caesarean section
Face-to-face EFT will be applied to mothers in the period after cesarean delivery in order to examine the effect of EFT application between 0-24 hours on womens pain level.
Measured: 0-24 hour
2. EFT for women with a planned cesarean section
Description: By applying EFT face-to-face to mothers in the period after cesarean delivery, the effect of EFT application between 0-24 hours on women's anxiety levels will be examined.
Measured: 0-24 hour
Secondary outcomes (1)
3.EFT for women with a planned cesarean section
EFT for women with a planned cesarean section
Remove Description: By applying EFT face-to-face to mothers in the period after cesarean delivery, the effect of EFT application between 0-24 hours on women's postpartum confidence levels will be examined.
Measured: 0-24 hour
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 May 2025
- Study start2 Jun 2025
- Primary completion1 Dec 2025
- Study completion13 Dec 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pain ManagementStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This study is a parallel randomized controlled trial on 60 primiparous women with cesarean section pain randomly allocated to EFT and control groups. The study was approved by the Ethics Committee of KTO Karatay University Faculty of Medicine. In addition, the protocol of this study was registered in the Clinical Trials Register. All participants gave written informed consent before data collection. Women were included according to the following criteria: at least primary school graduate, primiparous, planned cesarean section, and postoperative pain of 4 or more according to VAS. Women with chronic diseases such as heart disease, high blood pressure and diabetes, history of miscarriage, placenta previa, mental illness in the past year, use of psychoactive drugs, drug addiction, smoking, and pregnancy complications such as pre-eclampsia, bleeding, intrauterine death and preterm delivery were excluded.
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- KTO Karatay University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Hafize Dağ Tüzmen, KTO Karatay University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06999564
- Sponsor's protocol ID
- EFT AND CESAREAN SECTION
- Status last verified
- Dec 2025
- First submitted
- 13 Apr 2025
- Last updated
- 16 Dec 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: YES
Study at a glance
From the registry record, last updated by the sponsor on 16 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Eft applıed Before Cesarean sectıon on Postpartum feelıngs of Safety, anxıety and postoperatıve paın: RCT
- ClinicalTrials.gov ID
- NCT06999564
- Acronym / sponsor ID
- EFT AND CESAREAN SECTION
- Conditions
- Pain Management, Anxiety
- Keywords
- caesarean section, anxiety, sense of course
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- KTO Karatay UniversityUniversity, hospital or other
- Study start
- 2 Jun 2025 (actual)
- Primary completion
- 1 Dec 2025 (actual)
- Study completion
- 13 Dec 2025 (actual)
- First posted
- 31 May 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study is a parallel randomized controlled trial on 60 primiparous women with cesarean section pain, randomly divided into EFT and control groups. The study was approved by KTO Karatay University Faculty of Medicine Ethics Committee. Women will be included in the study according to the following criteria: at least primary school graduate, primiparous, planned cesarean section and 4 or more postoperative pain according to VAS. Women with chronic diseases such as heart disease, high blood pressure and diabetes, history of miscarriage, placenta previa, mental illness in the past year, psychoactive drug use, drug addiction, smoking, and pregnancy complications such as pre-eclampsia, bleeding, intrauterine death and preterm delivery will be excluded. Data collection will start in June 2025 and will be completed in August 2025.
Detailed description
Caesarean section is a surgical operation used when vaginal delivery is risky for the mother and fetus and can have both long and short-term effects on maternal and infant health. It is known that caesarean sections do not have a proven positive effect on mother-baby health, but may have negative consequences. After cesarean section, women may experience various problems such as inability to perform activities of daily living, breastfeeding problems, inability to actively take care of the newborn, decreased postpartum comfort, anxiety, depression, insomnia and pain.
Postoperative pain, one of the most common complications of cesarean section, plays an important role in ensuring skin-to-skin contact, establishing mother-baby bonding, initiating breastfeeding, the mother\'s recovery process and maternal-infant health. In addition, women may experience various levels of stress, anxiety and insecurity after cesarean section. Factors such as spousal support, presence of social support resources, attitudes of health personnel, antenatal education about the postpartum period, general well-being of mother and baby, stress, anxiety, depression, mode of delivery, perception of delivery, birth experience, breastfeeding problems, early discharge are factors affecting mothers\' sense of security in the postpartum period. Failure to provide a sense of security after birth increases the risk of anxiety and depression in the following periods. Factors that increase anxiety in women after cesarean section include surgical operation, prolonged transition to oral feeding, late mobilization, risk of infection, delayed mother-infant interaction and milk release.
Early detection of post-cesarean anxiety and postpartum sense of security and taking measures to address these conditions can improve the mother\'s quality of life, reduce anxiety and worry, and contribute to the effective and efficient maintenance of the mother-infant relationship. Reducing postoperative pain is also of great importance in terms of preventing physical complications and chronic pain, relieving depression, improving the quality of life of the individual, providing postpartum comfort and supporting effective breastfeeding. The side effects of pharmacologic methods used to improve postoperative pain and comfort after cesarean section and the inadequacy of these methods have increased the interest in non-pharmacologic approaches. Nonpharmacological techniques include diaphragmatic breathing exercises, Lamaze methods, visualization, meditation, acupuncture, acupressure, reflexology, massage, hypnosis, aromatherapy, prayer therapy, music therapy and EFT. EFT (Emotional Freedom Techniques) envisages pressing and stimulating the meridian crossing points of the organs associated with these emotions in order to improve psychological conditions such as anger, sadness and anxiety. EFT can resolve emotional problems, reduce anxiety levels, make the person feel calmer and think more positively, supporting maternal and fetal health.
A review of the literature shows that mothers have the most problems with pain, breastfeeding and mobilization after cesarean section and need help with these problems; 78% of women who gave birth by cesarean section experience moderate to severe pain, which negatively affects maternal comfort, and mothers who undergo cesarean section experience unbearable pain of different intensities. In the world, anxiety and depression in the postpartum period have increased in the last decade, as Hada et al. (2019) reported in their study. Postpartum depression rates have been reported to be approximately 13% worldwide. Postpartum anxiety and depression are more common in the early postpartum period and in women who gave birth by cesarean section.
EFT has been reported to be effective in many other areas, including the treatment of disorders such as generalized or specific anxiety, morbid fears, depression, posttraumatic stress disorder, chronic pain and addiction. However, so far, no study has examined the effect of EFT on postpartum feelings of safety, anxiety and postoperative pain together. In the light of this information, unlike the studies in the literature, this study will be conducted to examine the effect of EFT applied before cesarean section on postpartum feelings of safety, anxiety and postoperative pain. In this context, anxiety levels, pain intensity and postpartum feelings of safety will be evaluated in the post-cesarean period. Therefore, it is thought that the results obtained from the study will guide future studies and make a significant contribution to the literature.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- This study is a parallel randomized controlled trial on 60 primiparous women with cesarean section pain randomly allocated to EFT and control groups. The study was approved by the Ethics Committee of KTO Karatay University Faculty of Medicine. In addition, the protocol of this study was registered in the Clinical Trials Register. All participants gave written informed consent before data collection. Women were included according to the following criteria: at least primary school graduate, primiparous, planned cesarean section, and postoperative pain of 4 or more according to VAS. Women with chronic diseases such as heart disease, high blood pressure and diabetes, history of miscarriage, placenta previa, mental illness in the past year, use of psychoactive drugs, drug addiction, smoking, and pregnancy complications such as pre-eclampsia, bleeding, intrauterine death and preterm delivery were excluded.
| Arm | Type | Receives |
|---|---|---|
| EFT | Experimental | Behavioral: EFTThree sessions of face-to-face EFT will be applied to mothers who will have a planned cesarean section three days before delivery. In order to examine the effect of EFT on women's feelings of security, anxiety and pain levels after childbirth, face-to-face EFT will be applied to mothers in the postpartum period after cesarean section. |
| CONTROL | No intervention | –No application was made to the control group. Following the pre-test application, VAS, SUI and STAI-I-SATAI-II post-test data will be applied before and after cesarean delivery. After the data were reported, EFT was applied to the women in the control group individually by the researchers. |
Who may qualify
- Ages
- 18 to 35 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- primary school graduate
- primiparous
- planned cesarean section
- Postoperative pain of 4 or more according to VAS.
Key exclusion criteria (13 listed)
- Heart disease
- high blood pressure
- chronic diseases such as diabetes
- history of miscarriage
- placenta previa
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| EFTEFT involves the following steps: 1. Identification of the problem that is causing the person distress (e.g., fear of childbirth) and scoring or measuring the severity of this problem. 2. Tapping with the fingertips on certain points of the face and body, known as correction (i.e., regulation of the energy system), as well as the expression of an emphatic phrase (related to the person\'s problem and self-acceptance). | Behavioural | EFT |
Primary outcome
EFT for women who had a planned caesarean section
Time frame: 0-24 hour
Face-to-face EFT will be applied to mothers in the period after cesarean delivery in order to examine the effect of EFT application between 0-24 hours on womens pain level.
2. EFT for women with a planned cesarean section
Time frame: 0-24 hour
Description: By applying EFT face-to-face to mothers in the period after cesarean delivery, the effect of EFT application between 0-24 hours on women's anxiety levels will be examined.
1 secondary outcome
3.EFT for women with a planned cesarean section
Time frame: 0-24 hour
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Dec 2025.
- Individual participant dataSharing planned: Yes. YES
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing EFT in people with Pain Management and Anxiety, run by KTO Karatay University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 16 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
EFT for women who had a planned caesarean section (time frame: 0-24 hour). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Dec 2025.