Neuro Linguistic Programming Pain Levels After Cesarean Delivery

Pain, Postoperative Clinical Trial

Official title:

The Effect of Neuro Linguistic Programming on Pain Levels After Cesarean Delivery: A Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05033405
• Other study ID #: 047213793060212
• Status: Completed
• Phase: N/A
• Start date: March 1, 2021
• Est. completion date: June 21, 2021

Study information

• Verified date: August 2021
• Source: Munzur University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study was conducted to determine the effect of Neuro-Linguistic Programming (NLP) application on post-cesarean section pain levels.

Description:

The study was carried out between March 1 and June 1, 2021 with mothers who gave birth through cesarean section in the postpartum service of a maternity and children's hospital in the most populated city of Turkey, which is located in the west. The study data consists of a total of 76 individuals, including 38 in the experimental group and 38 in the control group. In the study, the effect size was calculated as 2.22. Accordingly, the power of the study, which was completed with 38 individuals in the control group and 38 in experimental group, had an effect size of 2.22, and used a significance level of 0.05, was calculated as 99.9%. The power analysis was conducted on the G*Power software package.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 76
• Est. completion date: June 21, 2021
• Est. primary completion date: June 1, 2021
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 19 Years to 42 Years

Eligibility

Inclusion Criteria:

• The study included individuals who

• had a cesarean section,

• were at the 6th to 24th hour postpartum,

• agreed to participate in the study,

• had a cesarean section for the first time,

• did not use patient-controlled analgesia (PCA),

• did not have an additional health problem that may cause pain in the postpartum period, other than cesarean incision pain, and

• could speak and understand Turkish.

Exclusion Criteria:

• Mothers who wanted to quit on their own will at any stage after being included in the study, had verbal communication problems, had hearing or vision problems, or had previously been diagnosed with a psychiatric illness were excluded from the sample.

Related Conditions & MeSH terms

• Nursing Caries
• Pain, Postoperative

Intervention

Behavioral:
• NEURO-LINGUISTIC PROGRAMMING (NLP)
? One session (20-minute long) of NLP application was performed. The NLP techniques that were employed were representational systems and submodality. In this technique, the sensory, auditory, and kinesthetic feelings of the individual are learned. These emotions are modified by imagining. The NLP application was carried out by a researcher who has a certificate in this field

Locations

Country	Name	City	State
Turkey	Nursel Alp Dal	Tunceli

Sponsors (1)

Lead Sponsor	Collaborator
Munzur University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Examination of inter-and intra-group differences regarding VAS Scores	A mean total score on the Visual Analogue Scale (VAS). In this assessment, users score their pain from 0 to 10. The scores are interpreted as follows: "0", no pain at all; 1-4, mild pain; 5-6, moderate pain; and 7-10, severe pain.; A mean total score on the VAS of four and above indicates postoperative pain.	Immediately after the completion of the NLP application
Secondary	Distribution of participant characteristics by groups	The effect of NLP application on post-operative pain in women who gave birth by cesarean section is examined. Comparisons are made by using Visual Analog Scale (VAS) mean scores in the experimental and control groups.	20 minutes after the first administration of the VAS