Neurolinguistic Programming on Labor Pain

Labor Pain Clinical Trial

Official title:

The Effect of Neurolinguistic Programming on Labor Pain, Fear, Duration and Maternal Satisfaction

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06070779
• Other study ID #: NLP and labor pain
• Status: Recruiting
• Phase: N/A
• Start date: October 1, 2023
• Est. completion date: February 28, 2024

Study information

• Verified date: January 2024
• Source: University of Gaziantep
• Contact: AYSEGÜL KILIÇLI, Dr.
• Phone: (0414) 317 17 17
• Email: aysegul_ay_9[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

THE EFFECT OF NEURO LINGUISTIC PROGRAMMING ON LABOUR PAIN, FEAR, DURATION AND MATERNAL SATISFACTION

Description:

In this study, it is aimed to determine the effect of neuro linguistic programming on labour pain, fear, duration and maternal satisfaction.

Sample size:

• The sample size of the study is 124 (for primiparous=62, multiparous=62).

• Frist, primiparous women who applied to the hospital for vaginal delivery will be divided into 2 arms as 31 experimental group and 31 control group.

• Second, multiparous women who applied to the hospital for vaginal delivery will be divided into 2 arms as 31 experimental group and 31 control group.

Data Collection Tools;

• Introductory Information Form,

• Visual Analog Scale for Pain,

• Wijma Birth Expectation/Experience Scale B version,

• Birth Satisfaction Scale

Application time:

• The neurolinguistic programming will be applied to the experimental group. NLP application will be done when the cervical opening is 4 cm, when the cervical opening is 5-6 cm, when the cervical opening is 7-8 cm.NLP application will be done three times in total. Each session will last 20 minutes

• No neurolinguistic programming will be applied to the control group.

Measurement time:

• Introductory Information Form will be completed by the woman when the cervical dilatation is 3-4 cm.

• VAS for pain will be measured before and immediately after the application when cervical dilatation is 4 cm; before and immediately after the application when cervical dilatation is 5-6 cm; before and immediately after the application when cervical dilatation is 7-8 cm; when cervical dilatation is 9-10 cm.

• Wijma Birth Expectation/Experience Scale B version and Birth Satisfaction Scale will be completed by the woman in the postnatal ward at approximately the second hour postpartum after the birth has taken place.

• The labour duration will be started for the mother who comes to the delivery room when the cervical opening is 4 cm and the total labour duration will be measured in minutes after the birth occurs.

• The control group will not be administered NLP only, but the measurements will be completed as in the experimental group.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 124
• Est. completion date: February 28, 2024
• Est. primary completion date: February 28, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 19 Years to 35 Years

Eligibility

Inclusion Criteria:

• pregnant women who give birth vaginally,

• whose birth takes place in the delivery room unit,

• who are 19 years of age or older and 35 years of age or younger,

• who are born at 37 and above gestational weeks,

• who give singleton birth,

• who do not have chronic diseases and any complications in this pregnancy and postpartum period

Exclusion Criteria:

• mothers who wish to leave the study voluntarily at any stage after being included in the study,

• who develop any health problems in themselves or their babies during the birth and postnatal period will be excluded from the scope.

Related Conditions & MeSH terms

• Labor Pain

Intervention

Other:
• neuro linguistic programming
neuro linguistic programming

Locations

Country	Name	City	State
Turkey	Sanliurfa training and research hospital	Sanliurfa	Eyalet/Yerleske

Sponsors (1)

Lead Sponsor	Collaborator
Aysegul Kilicli

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual Analogue Scale for Pain	Visual Analogue Scale for Pain; Scores between 0-10 are received. The difference in score indicates that the pain is aching.	immediately before neuro linguistic programming application when the cervical opening was 4 cm, 5-6 cm, 7-8 cm
Primary	Visual Analogue Scale for Pain	Visual Analogue Scale for Pain; Scores between 0-10 are received. The difference in score indicates that the pain is aching.	immediately after neurolinguistic programming application when the cervical opening was 4 cm, 5-6 cm, 7-8 cm
Primary	Wijma Birth Anticipation/Experience Scale B version;	Wijma Birth Anticipation/Experience Scale B version; The minimum score from the scale is 0 and the maximum score is 165 points. If the total score obtained from the scale is below 66, it is considered mild, between 66 and 85, it is considered moderate, and above 85, it is considered severe fear of childbirth.	between approximately the second to sixth hours postpartum
Primary	Birth Satisfaction Scale;	Birth Satisfaction Scale; The score that can be obtained from the scale is between 30-150 points. The change in the score obtained from the scale from birth increases.	between approximately the second to sixth hours postpartum
Primary	Labour duration	Labour duration; time will be measured in minutes	the duration of labour will be calculated in minutes from the time the cervical opening begins until the fourth stage of labour
Primary	Visual Analogue Scale for Pain	Visual Analogue Scale for Pain; Scores between 0-10 are received. The difference in score indicates that the pain is aching.	when the cervical opening was 9-10 cm