Effects of Yakson Method and Swaddling on Pain and Physiological Parameters

NCT ID: NCT05518916

Last Updated: 2022-08-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-01

Study Completion Date

2023-09-01

Brief Summary

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Type of Study: The study was planned to be conducted in a randomized controlled experimental design.

Place and Time of the Research: Institutional permission will be obtained from the Balcalı Training and Research Hospital in Adana for the collection of research data. Researchers commit to start data collection after obtaining institutional permission. The data collection process will take 1 year after obtaining the institutional permission.

48 newborns who are suited the inclusion criteria will be included in the study. Participants will be assigned to 3 groups according to randomization: Swaddling, Yakson Method, and Control.

Detailed Description

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Total processing time and baby's crying time are calculated by watching video recordings. In order to find the total procedure time, starting from the puncture of the baby's heel, the time until the dry cotton is placed on the baby's heel after the blood collection process is completed is calculated. The heart rate and SpO2 are noted by the investigator during the heel lancing procedure. Pain assessment of infants is done by two independent neonatal nurses, apart from the researcher, by watching video recordings. The scores given by the two observers will be evaluated by making inter-observer harmony. Before the evaluation, the nurses will be trained about the scale and its evaluation.

Conditions

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Pain During Heal Lancing

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Prospective, parallel, three-arm randomized controlled clinical trial
Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Outcome Assessors
After the researh report is written, a third person will assign an intervention and control group to the letters.

Study Groups

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Yakson Method Group

* The mother is informed about the benefits of the Yakson method.
* Yakson method is taught practically to the mother. Education continues until the researcher is sure that the mother has done the method correctly. The mother starts the application 10 minutes before the heel lancing is done and continues for another 5 minutes after the heel lancing is done. During the application, the baby is recorded with the camera. Just before starting the Yakson method (initial assessment), at 10 minutes of the Yakson method (just before the heel lancing), during the heel lancing while the Yakson method is in progress, and 5 minutes after the procedure (just before the end of the tender touch), the newborn's pain and physiological parameters are evaluated. Evaluation results are recorded in the application observation form.

Group Type EXPERIMENTAL

Nonfarmacology method

Intervention Type OTHER

Yakson Method and Swaddling

Swaddling Group

* Parents are informed about the research and verbal consent is obtained.
* Written consent is obtained with an informed consent form.
* The Mother-Baby Information Form is filled.
* Babies are fed 1 hour before blood collection.
* And researher swaddling the baby

Group Type EXPERIMENTAL

Nonfarmacology method

Intervention Type OTHER

Yakson Method and Swaddling

Control Group

Parents are informed about the research and verbal consent is obtained.

* Written consent is obtained with an informed consent form.
* The Mother-Baby Information Form is filled.
* Babies are fed 1 hour before blood collection.
* Before starting the heel lancing, a pulse oximeter probe will be attached to the baby's left big toe.
* Blood is taken from the right heel of the foot.
* During the application, the baby is recorded with the camera.
* Evaluation results are recorded in the application observation form.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Nonfarmacology method

Yakson Method and Swaddling

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Born at term (38-42 weeks)
* Healthy newborn
* Absence of congenital anomaly
* No analgesic or sedative medication has been administered in the last 6 hours
* Parent's consent for inclusion in the study in accordance with the consent form


* Mother's willingness to participate in the study
* The mother can be mobilized and not have a physical disability (so that she can appyl Yakson therapy for her baby)
* Being communicative

Exclusion Criteria

* Babies whose blood cannot be drawn on the first try
Minimum Eligible Age

0 Days

Maximum Eligible Age

28 Days

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Istanbul University - Cerrahpasa

OTHER

Sponsor Role lead

Responsible Party

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Aslihan Hacisalihoglu

Research Assistan

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Aslıhan Hacısalihoğlu, Master

Role: CONTACT

03223386841

Birsen Mutlu, PHD

Role: CONTACT

03223386842

Other Identifiers

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IstanbulUC-AHacisalihoglu

Identifier Type: -

Identifier Source: org_study_id

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