Neurolinguistic Programming on Labor Pain

Status Recruiting

Clinical Trial Summary

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

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Labor Pain

Clinical Trial Details

NCT number	NCT06070779
Study type	Interventional
Source	University of Gaziantep
Contact	AYSEGÜL KILIÇLI, Dr.
Phone	(0414) 317 17 17
Email	aysegul_ay_9@hotmail.com
Status	Recruiting
Phase	N/A
Start date	October 1, 2023
Completion date	February 28, 2024

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT03539562` - Therapeutic Rest to Delay Admission in Early Labor: A Prospective Study on Morphine Sleep
Withdrawn	`NCT04662450` - Evaluation and Management of Parturients' Pain Intensity	N/A
Completed	`NCT02885350` - Spinal or Epidural Fentanyl or Sufentanil for Labour Pain in Early Phase of the Labour	Phase 4
Completed	`NCT02550262` - Programmed Intermittent Epidural Bolus for Labor Analgesia During First Stage of Labor	N/A
Completed	`NCT01598506` - Intrathecal Hydromorphone for Labor Analgesia	Phase 2
Withdrawn	`NCT01636999` - Comparing Sedara to Butorphanol in Early Labor	N/A
Completed	`NCT00987441` - Epidural Labor Analgesia and Infant Neurobehavior	N/A
Completed	`NCT00755092` - Effect of Doula in Nulliparas and Multiparas	N/A
Terminated	`NCT00787176` - The Association Between Fluid Administration, Oxytocin Administration, and Fetal Heart Rate Changes	N/A
Recruiting	`NCT06036797` - Efficacy and Safety of Hydromorphone-ropivacaine Versus Sufentanil-ropivacaine for Epidural Labor Analgesia	Phase 2
Completed	`NCT05512065` - Changes in Velocimetric Indices of Uterine and Umbilical Arteries Before and After Combined Spinal-epidural Analgesia in Laboring Women	N/A
Completed	`NCT05327088` - Epidural Dexmedetomidine vs Nalbuphine for Labor Analgesia	Phase 2
Completed	`NCT03103100` - Comparing Bupivacaine, Lidocaine, and a Combination of Bupivacaine and Lidocaine for Labor Epidural Activation	Phase 3
Recruiting	`NCT03623256` - Comparison of Intrathecal Versus Epidural Fentanyl on Fetal Bradycardia in Labor Combined Spinal Epidural Analgesia	Phase 4
Active, not recruiting	`NCT02271100` - Assessment of the Use of Ultrasound for Epidural Catheter Placement and Comparison With Palpation Technique	N/A
Completed	`NCT02926469` - Virtual Reality Analgesia in Labor: The VRAIL Pilot Study	N/A
Completed	`NCT03712735` - Programmed Intermittent Epidural Bolus For Laboring Obstetrical Women	Phase 4
Not yet recruiting	`NCT05565274` - Outcome of Combined Tramadol and Paracetamol Versus Pentazocine as Labour Analgesia Among Parturients	N/A
Recruiting	`NCT01708668` - The Effects of Intermittent Epidural Bolus on Fever During Labor Analgesia	N/A
Recruiting	`NCT02575677` - Oxycodone in Treatment of Early Labour Pain Efficacy and Safety

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.