Evaluation of Comfort Behavior Levels of Newborns With Artificial Intelligence Techniques

Sponsor

Eskisehir Osmangazi University (Other)

Overall Status

Unknown status

CT.gov ID

NCT04337229

Collaborator

(none)

1,000

Enrollment

Arm

Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

This study; It will be carried out with the aim of developing the artificial intelligence method, which allows automatic determination of comfort levels of newborns.

Condition or Disease	Intervention/Treatment	Phase
Newborn Comfort Nursing Artificial Intelligence	Other: Artifical intelligent	N/A

Detailed Description

This study; It will be carried out with the aim of developing the artificial intelligence method, which allows automatic determination of comfort levels of newborns. Facial and body movements of newborns will be recorded by camera, and images will be processed in computer environment by using artificial intelligence techniques. As a result, it is planned to create a technology that determines the comfort level of the newborn quickly and simply and can be used by the mobile device.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

1000 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Intervention Model Description:

it is planned to create a technology that determines the comfort level of the newborn quickly and simply, easy to use, time-saving and can be used by the mobile device.it is planned to create a technology that determines the comfort level of the newborn quickly and simply, easy to use, time-saving and can be used by the mobile device.

Masking:

None (Open Label)

Masking Description:

Researchers and family of newborns will know about all the details of the study. Verbal and written permission will be obtained from families.

Primary Purpose:

Other

Official Title:

Evaluation of Comfort Behavior Levels of Newborns With Artificial Intelligence Techniques

Anticipated Study Start Date :

Sep 1, 2020

Anticipated Primary Completion Date :

Dec 1, 2020

Anticipated Study Completion Date :

Sep 1, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: artificial intelligence techniques Facial and body movements of newborns will be recorded by camera, and images will be processed in computer environment by using artificial intelligence techniques. As a result, it is planned to create a technology that determines the comfort level of the newborn quickly and simply and can be used by the mobile device.	Other: Artifical intelligent it is planned to create a technology that determines the comfort level of the newborn quickly and simply, easy to use, time-saving and can be used by the mobile device.

Arm

Intervention/Treatment

Experimental: artificial intelligence techniques

Facial and body movements of newborns will be recorded by camera, and images will be processed in computer environment by using artificial intelligence techniques. As a result, it is planned to create a technology that determines the comfort level of the newborn quickly and simply and can be used by the mobile device.

Other: Artifical intelligent

it is planned to create a technology that determines the comfort level of the newborn quickly and simply, easy to use, time-saving and can be used by the mobile device.

Outcome Measures

Primary Outcome Measures

Images of the newborn [12 hours for each newborn]
Images will be taken to transfer behaviors of newborns to the computer. Attention will be paid to making face and body movements visible while taking the image.The camera will take 12 hours of view of each newborn.However, this period can be shortened as a result of preliminary work.

Secondary Outcome Measures

Artificial intelligence techniques [Approximately 1 week for each newborn]
The images of the newborn will be transferred to the computer. The images will be processed by a specialist on computer using artificial intelligence techniques.

Eligibility Criteria

Criteria

Ages Eligible for Study:

1 Hour to 28 Days

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Parents' acceptance of their baby's participation in the study
Having a baby born at 24-42 weeks

Exclusion Criteria:

Having a baby born before 24 weeks of gestation or after 42 weeks of gestation.
Has received analgesic, muscle relaxant or sedative drug treatment that may affect comfort and behavior (last 24 hours)
Newborn has serious neurological damage

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

Eskisehir Osmangazi University

Investigators

Principal Investigator: DENİZ YİĞİT, Res.Asst., ESKİŞEHİR OSMANGAZİ ÜNİVERSİTESİ SAĞLIK BİLİMLERİ FAKÜLTESİ

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

DENİZ YİĞİT, Research Assistant, Eskisehir Osmangazi University

ClinicalTrials.gov Identifier:

NCT04337229

Other Study ID Numbers:

DYIGIT
Ayfer ACIKGOZ

First Posted:

Apr 7, 2020

Last Update Posted:

Apr 13, 2020

Last Verified:

Apr 1, 2020

Individual Participant Data (IPD) Sharing Statement:

Yes

Plan to Share IPD:

Yes

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Keywords provided by DENİZ YİĞİT, Research Assistant, Eskisehir Osmangazi University

newborn

comfort

nursing

artificial intelligence

Study Results

No Results Posted as of Apr 13, 2020