NCT06070779

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
124

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 18, 2023

Completed
15 days until next milestone

Study Start

First participant enrolled

October 3, 2023

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 6, 2023

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 21, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 21, 2024

Completed
Last Updated

September 19, 2024

Status Verified

September 1, 2024

Enrollment Period

4 months

First QC Date

September 18, 2023

Last Update Submit

September 3, 2024

Conditions

Keywords

neuro linguistic programmingLabour painLabour fearLabour satisfactionLabour duration

Outcome Measures

Primary Outcomes (6)

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

Study Arms (4)

neuro linguistic programming group for primiparous

EXPERIMENTAL

NLP application to the experimental group will be done by the researcher Ayşegül Kılıçlı. The application session will 20 minutes. The application will be started in the active phase of labour when the cervical opening is 4 cm. In the neuro linguistic programming (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 programming

control group for primiparous

NO INTERVENTION

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

neuro linguistic programmig group for multiparous

EXPERIMENTAL

NLP application to the experimental group will be done by the researcher Ayşegül Kılıçlı. The application session will 20 minutes. The application will be started in the active phase of labour when the cervical opening is 4 cm. In the neuro linguistic programming (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 programming

control group for multiparous

NO INTERVENTION

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

Interventions

neuro linguistic programming

neuro linguistic programmig group for multiparousneuro linguistic programming group for primiparous

Eligibility Criteria

Age19 Years - 35 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailspregnant women
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Şanlıurfa training and research hospital

Sanliurfa, Eyalet/Yerleşke, 63000, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Labor Pain

Interventions

Neurolinguistic Programming

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Models, NeurologicalModels, BiologicalModels, TheoreticalInvestigative TechniquesModels, PsychologicalPsycholinguisticsBehavioral SciencesBehavioral Disciplines and Activities

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: randomised controlled trial
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Gaziantep University Health Sciences Institute, Department of Nursing, Department of Obstetrics and Gynaecology Nursing, PhD.

Study Record Dates

First Submitted

September 18, 2023

First Posted

October 6, 2023

Study Start

October 3, 2023

Primary Completion

January 21, 2024

Study Completion

January 21, 2024

Last Updated

September 19, 2024

Record last verified: 2024-09

Data Sharing

IPD Sharing
Will not share

Locations