RecruitingNot ApplicableNCT05486663

Tactile/kinesthetic Stimulus Program

The Effect of the Tactile/kinesthetic Stimulus Program on the Maturation of Sucking Ability in Preterm Infants


Sponsor

Gonca Karatas Baran

Enrollment

80 participants

Start Date

Aug 1, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

The study will be carried out as a prospective randomized controlled clinical study to determine the effect of tactile/kinesthetic stimulus program on preterm infants on transition time to full sucking, sucking success and hospital stay.


Eligibility

Min Age: 28 WeeksMax Age: 32 Weeks

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Tactile/kinesthetic Group for people with breast feeding, exclusive, hospital stay, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 28 Weeks to 32 Weeks.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERTactile/kinesthetic Group

Tactile/kinesthetic stimulation is performed in three stages. In the first stage; for tactile stimulation; The baby is placed in the prone (prone) position in the incubator. Light massage was applied in the head, shoulder, back, legs and arms of the infants. Each massage is applied 12 times for 1 minute. Massage was performed for 5 seconds. In the second stage Kinesthetic stimulation, including elbow flexion-extension movement, palm massages, flexion-extension of the knees and legs and plantar massages, was applied while the neonate was in supine position. Each kinesthetic stimulation was performed for 5 seconds. Each movement was repeated six times, with a total duration of 5 minutes. Tactile stimulation was repeated once after kinesthetic stimulation. The total duration of TKS was 15 minutes which was performed three times daily preferably between breastfeeding or bottle feeding for 14 consecutive days.


Locations(1)

Etlık Zubeyde Hanım Kadın Hastalıkları Eğitim Ve Araştırma Hastanesi

Ankara, Eyalet/Yerleşke, Turkey (Türkiye)

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05486663


Related Trials