Neurolinguistic Programmig on Labor Pain

Sponsor
Aysegul Kilicli (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06070779
Collaborator
(none)
124
4
4

Study Details

Study Description

Brief Summary

THE EFFECT OF NEURO LINGUISTIC PROGRAMME ON BIRTH PAIN, FEAR, DURATION AND MATERNAL SATISFACTION

Condition or Disease Intervention/Treatment Phase
  • Other: neuro linguistic program
N/A

Detailed Description

In this study, it is aimed to determine the effect of neuro linguistic programme on birth 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.

Randomization:
  • primiparous women will be randomly assigned to the experimental and control groups. 31 pieces of paper labelled experiment and 31 pieces of paper labelled control will be placed in sealed opaque envelopes and mixed in a bag. The women will be asked to choose one envelope. The information in the envelope will not be told to the mothers.

  • multiparous women will be randomly assigned to the experimental and control groups. 31 pieces of paper labelled experiment and 31 pieces of paper labelled control will be placed in sealed opaque envelopes and mixed in a bag. The women will be asked to choose one envelope. The information in the envelope will not be told to the mothers.

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 program will be applied to the experimental group once during the latent phase of labour (when the cervical opening is 4-6 cm). The application will last 20 minutes.

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

Measurement time:
  • Introductory Information Form and Visual Analogue Scale for Pain will be filled in the experimental group before the application.

  • Visual Analogue Scale for Pain, Wijma Birth Expectation/Experience Scale B version, Birth Satisfaction Scale will be filled after the application.

  • The time will be started for the mother who comes to the delivery room when the cervical opening is 4 cm and the total delivery time 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
124 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
randomised controlled trialrandomised controlled trial
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
The Effect of Neurolinguistic Programmig on Labor Pain, Fear, Duration and Maternal Satisfaction
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Feb 1, 2024
Anticipated Study Completion Date :
Feb 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: neuro linguistic programming group for primiparous

NLP application to the experimental group will be done only once by the researcher Ayşegül Kılıçlı. Application will last 20 minutes.The practice will be initiated in the latent phase of labour when the cervical opening is 4 cm. In the neuro linguistic program (NLP); The system of representation of women in practice will be determined first. Then, with the anchoring technique, negative feelings and thoughts about labour will be tried to be erased from the mind or their severity will be reduced. Then, positive feelings and thoughts will be created instead of the mother's negative feelings and thoughts with belief change strategies. Then, with the swish technique, the mother's positive feelings and thoughts about labour will be made aware of and reinforced.

Other: neuro linguistic program
neuro linguistic programming

No Intervention: control group for primiparous

The control group will not receive only the neuro-linguistic program, but all other assessments will be parallel to the experimental group (neuro linguistic programming group for primiparous).

Experimental: neuro linguistic programmig group for multiparous

NLP application to the experimental group will be done only once by the researcher Ayşegül Kılıçlı. Application will last 20 minutes.The practice will be initiated in the latent phase of labour when the cervical opening is 4 cm. In the neuro linguistic program (NLP); The system of representation of women in practice will be determined first. Then, with the anchoring technique, negative feelings and thoughts about labour will be tried to be erased from the mind or their severity will be reduced. Then, positive feelings and thoughts will be created instead of the mother's negative feelings and thoughts with belief change strategies. Then, with the swish technique, the mother's positive feelings and thoughts about labour will be made aware of and reinforced.

Other: neuro linguistic program
neuro linguistic programming

No Intervention: control group for multiparous

The control group will not receive only the neuro-linguistic program, but all other assessments will be parallel to the experimental group (neuro linguistic programmig group for muliparous).

Outcome Measures

Primary Outcome Measures

  1. Labour Pain [immediately before application]

    Visual Analogue Scale for Pain

  2. Labour Pain [immediately after application]

    Visual Analogue Scale for Pain

  3. Labour fear [immediately after application]

    Wijma Birth Anticipation/Experience Scale B version

  4. Birth satisfaction [in the sixth hour after birth]

    Birth Satisfaction Scale

  5. birth time [the duration of labour will be calculated in minutes from the time the cervical opening begins until the fourth stage of labour]

    birth time

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years to 35 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Aysegul Kilicli

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Aysegul Kilicli, Gaziantep University Health Sciences Institute, Department of Nursing, Department of Obstetrics and Gynaecology Nursing, PhD., University of Gaziantep
ClinicalTrials.gov Identifier:
NCT06070779
Other Study ID Numbers:
  • NLP and labor pain
First Posted:
Oct 6, 2023
Last Update Posted:
Oct 6, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Aysegul Kilicli, Gaziantep University Health Sciences Institute, Department of Nursing, Department of Obstetrics and Gynaecology Nursing, PhD., University of Gaziantep
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 6, 2023