The Effect Of Therapeutic Touch To Mothers With Preterm Babies

October 9, 2019 updated by: Seyda Can, University of Yalova

The Effect Of Therapeutic Touch Training Given To Mothers With Preterm Babies On Attachment Level And The Responses The Baby

The study was carried to determine the effect of yakson or gentle human touch methods applied by the mothers to their preterm newborns on mother's attachment level and baby's response.

Study Overview

Detailed Description

The study was carried out as a randomized controlled experimental research. Population of the study is all of the babies who were hospitalized at the neonatal intensive care unit of a state hospital in Turkey between August 2016 and August 2017 and the mothers of the babies; its sample is 90 mothers and their babies included with randomization method who were matching the criteria who were also hospitalized between these dates.

Study Type

Observational

Enrollment (Actual)

90

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The sample of the study consists of babies and their mothers who were matching the criteria of the research between these dates and who volunteered. As a result of the power analysis, sample size was calculated as 90 for experimental and control groups with Power: 0.80. As a result of the sample calculation a total of 90 mothers and babies; 30 for Yakson group, 30 for gentle human touch group, 30 for control group were included in the study. The assignment of mothers and babies to the experiment and control groups was carried out by randomization with drawing lots method.

Description

Inclusion Criteria:

Mothers' Selection Criteria

  • Mother should not have any defines psychiatric diseases,
  • Mother should not have any physical disabilities,
  • Mother should be literate and open to communication,
  • Should not have transportation problem,
  • Should be willing to participate and volunteer for the study.

Babies' Selection Criteria

  • Babies should be between 26-34 gestation weeks,
  • Should not have congenital abnormalities,
  • Babies should not have any health problems that may hinder the practice (Intracranial hemorrhage, sepsis, hemorrhagic diseases, having an operation, etc.).

Exclusion Criteria:

-Participants must have inclusion criterias.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Control
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Control Group

The mothers and infants in the experimental and control groups were assigned to the groups by randomization method. Therapeutic touch didn't apllied to control group.

Babies in the control group who took care practices in accordance with normal hospital procedures.

The study was carried out as randomized experiment to determine the effect of Yakson or Gentle Human Touch method practiced by mothers to preterm newborns on the maternal attachment level and the baby's responses.
Other Names:
  • The Effect Of Yakson Or Gentle Human Touch
Yakson Group

The touch method was taught to the mothers in the Yakson group by the researcher in the first three days after the birth with the training brochure, video and applications on the model that are prepared in accordance with expert opinion.

In yakson method, mother's fingers are closed, and she should touch in a way that does not apply excessive pressure. The method is applied for a total of 15 minutes in three cycles. First 5 minutes is resting the hand, 5 minutes is gentle caressing, and another 5 minutes of resting the hand.

The study was carried out as randomized experiment to determine the effect of Yakson or Gentle Human Touch method practiced by mothers to preterm newborns on the maternal attachment level and the baby's responses.
Other Names:
  • The Effect Of Yakson Or Gentle Human Touch
Gentle Human Touch Group

The touch method was taught to the mothers in the Gentle Human Touch group by the researcher in the first three days after the birth with the training brochure, video and applications on the model that are prepared in accordance with expert opinion.

Mother slowly places one hand on the baby's hand and the other over pelvic cavity, covering the waist and hips of the baby.

The touch is preserved for 15 minutes. In order to ensure equal touch for the duration of gentle human touch, the mother sits on a stool and her elbows have to be at the same level with baby's bed

The study was carried out as randomized experiment to determine the effect of Yakson or Gentle Human Touch method practiced by mothers to preterm newborns on the maternal attachment level and the baby's responses.
Other Names:
  • The Effect Of Yakson Or Gentle Human Touch

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Effect Of Therapeutic Touch Training Given To Mothers With Preterm Babies On Attachment Level And The Responses The Baby
Time Frame: Between August 2016 and August 2017
Study was determined that therapeutic touch methods applied to babies by the mothers increase mother-baby attachment; contributed to the sleep-calmness states, vital signs and weight gain of the baby; and reduced the stays in hospital.
Between August 2016 and August 2017

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: ŞEYDA CAN, PhD, University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2016

Primary Completion (Actual)

August 31, 2017

Study Completion (Actual)

August 31, 2017

Study Registration Dates

First Submitted

October 8, 2019

First Submitted That Met QC Criteria

October 8, 2019

First Posted (Actual)

October 10, 2019

Study Record Updates

Last Update Posted (Actual)

October 14, 2019

Last Update Submitted That Met QC Criteria

October 9, 2019

Last Verified

October 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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