The Effect of Pain Management Education on The Mothers in Newborn

Pain Clinical Trial

Official title:

The Effect of Pain Management Education on The Mothers on The Use of Nonpharmacological Practices and Anxiety Level in Heel Stick in Newborn

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05173662
• Other study ID #: SelcukU-11-2021
• Status: Completed
• Phase: N/A
• Start date: July 10, 2021
• Est. completion date: November 24, 2021

Study information

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

Clinical Trial Summary

The aim of this study was to determine the effect of non-pharmacological pain management education given to mothers on the use of non-pharmacological methods and anxiety levels of mothers during routine heel blood collection (guthrie screening test) in term newborns.

H0= There was no difference between the intervention group who received non-pharmacological pain management education and the control group's level of anxiety and use of non-pharmacological applications.

H1= The use of non-pharmacological methods is different between the intervention group and the control group that received non-pharmacological pain management education.

H2= Anxiety scores of the intervention group that received non-pharmacological pain management education and the control group were different.

H3= Some characteristics and anxiety levels of mothers have an effect on their use of non-pharmacological methods.

It was carried out between July - September 2021 at the Akşehir State Hospital Gynecology and Obstetrics Clinic, which serves in the Akşehir district of Konya province.

Description:

In this study was to determine the effect of pain management education on mothers' use of non-pharmacological methods and anxiety levels during newborn heel blood screening.

This study was designed as parallel group, pre-test and post-test randomized controlled trial.

Based on 80% power and 95% confidence level, the sample size was calculated as 32 infants for each group, a total of 64 infants (G*Power 3.1.9.2).

Randomization In this study, stratified randomization method was applied. Eight blocks of four were created with the permutation-blocked randomization method.

With the computer program (randomized.org), the numbers from 1 to 6 were listed 8 times (6,3,5,2,2,6,6,5) and the combinations were sorted according to this group, and assignments were made to the intervention and control groups.

Blinding The researcher and participant (mothers) could not be blinded since the researcher had to provide training and manage the process before the application. In order to avoid bias in the evaluation of the data, the analysis of the coded data in terms of groups was done by an independent statistician. After the statistical analyzes were completed and the research report was written, the researcher explained the coding of the intervention and control groups. In this way, single blindness was achieved.

In the collection of research data; Introductory Information Form, Non-pharmacological Method Application Checklist and Spielberger State Anxiety Inventory were used. In addition, the mothers in the intervention group were given a brochure on Nonpharmacological Pain Management Education Nonpharmacological Pain Management Education Brochure

This brochure was prepared by the researcher in line with the literature .The brochure contains methods for non-pharmacological pain management that can be applied during procedural painful interventions in newborns. These methods are; expressed breast milk, hugging, skin-to-skin contact, cuddling, calming sounds. The brochure contains information and drawings about the methods. The drawings were created by Architect Merve Özkald. Opinions were received from five experts in terms of the content, language, design and visual suitability of the brochure and the Content Validity Index (CGI) was calculated as 0.890.

Data collection Voluntary Informing Consent Form was obtained from the mothers before the study, and the Introductory Information Form was collected from the mothers by the researcher by face-to-face interview method. Between the dates of the study, mothers of newborns who met the inclusion criteria were randomly assigned to intervention and control groups. Heel blood collection in all newborns; The study was carried out between the 24th and 48th hours of the baby's life, in the gynecology and obstetrics clinic, only in the room where the mother and baby stay together, without any intervention to the baby, by removing the clothes from the lower part of the baby in its natural position.

The heel blood collection procedure was applied in such a way that the baby was next to the mother. No non-pharmacological method was used in routine practice during the procedure.

In this study; The heel blood collection procedure was performed by the same nurse working in the NICU for each infant at one time and by taking the same amount of blood from each infant on average.

At least half an hour before the heel blood collection, it was ensured that the babies were fed and their diapers were clean. During the blood collection process; Standardization of the blood collection technique used, the area where the blood was taken (outer side of the right heel), the needle used in the procedure (needle number 21), environmental factors (such as heat, light, noise), used antiseptic solution (70% alcohol) provided.

To the mothers in the intervention group; At least 12 hours before the heel blood collection (guthrie screening test), information was given by the researcher (FU) about the purpose of the heel blood collection procedure and the application process, and the questions, if any, were answered. Afterwards, an average of 25 minutes of education was given through the training brochure prepared by the researcher on non-pharmacological pain management. The education was carried out in a language that the mother could understand, in the form of direct lectures and questions and answers, using the visuals in the brochure.

The mothers in the control group, on the other hand, were informed by the researcher about the purpose of the heel blood collection procedure and the application process at least 12 hours before the guthrie screening test, and their questions were answered, if any, and no other application was made.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 64
• Est. completion date: November 24, 2021
• Est. primary completion date: September 24, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 38 Weeks to 42 Weeks

Eligibility

Inclusion Criteria:

For newborns;

• Being a healthy term newborn (born at 38-42 weeks of gestation)

• A blood sample will be taken for the Guthrie screening test.

• Having the mother with the baby (Gynecology and Obstetrics Clinic) for mothers;

• Volunteering to participate in the study

• Ability to read and write Turkish

• Being over 18 years old

Exclusion Criteria:

For newborns;

• Having a congenital anomaly

• Having received any analgesia before the procedure

• IInability to draw blood in one go for mothers;

• Rejection of heel blood collection voluntarily

• Existence of any obstacle that may make communication difficult

Related Conditions & MeSH terms

• Infant ALL
• Pain
• Pain, Procedural
• Procedural Pain

Intervention

Procedure:
• Providing education and brochures on non-pharmacological methods that can be applied during the heel blood collection process
Theeduvation initiative was implemented by the researcher at least 12 hours ago in the mothers' room and a brochure was given about the education.

Locations

Country	Name	City	State
Turkey	Selcuk University	Konya	Selcuklu
Turkey	Selcuk University	Konya

Sponsors (1)

Lead Sponsor	Collaborator
Selcuk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The mothers' use of non-pharmacological methods	The mothers' use of non-pharmacological methods during heel blood collection. These methods are; expressed breast milk, hugging, skin-to-skin contact, cuddling, calming sounds. The cases of using the methods were determined as yes and no for each method.	After the process first 10 minute
Secondary	State anxiety level scores of mothers	The State and Trait Anxiety Inventory (STAI) was developed by Spielberger in 1983.; The STAI consists of two subscales of 20 questions about state and trait anxiety.; All questions are in a four-point Likert type. The scores of both subscales are summed separately and a total score between 20 and 80 is obtained.; Higher scores indicate a higher level of anxiety.	Pre-test 5-10 minutes before the process and 10 minutes after the process