The Effects of Whole Body Prenatal Massage Therapy During Pregnancy: A Randomized Controlled Experimental Trial

August 10, 2021 updated by: Yeliz CAKIR KOCAK, Ege University

The Effects of the One Hour-Whole Body Prenatal Massage Therapy Session on Prenatal Distress and Prenatal Attachment for Women and Their Fetuses During Late Pregnancy: A Randomized Controlled Experimental Trial

Background: Massage therapy in many parts of the world is used in all periods of pregnancy.

Aim: The study aimed to determine the effect of massage therapy during pregnancy on women and their fetuses in a university hospital in Izmir, Turkey.

Method: A randomized controlled experimental trial was aimed to reach primipara pregnant women, 20-35 years old, who came to a university obstetric clinic to get the results of the first-trimester screen test. Researchers aimed to reach 30 pregnant women at the start of the study. Participants were randomly allocated to a parallel comparison group by a central office. The sampling technique has been applied according to the CONSORT criteria.

The study practices have been carried out after receiving ethics committee and institution approvals after the researcher completed the prenatal massage therapy training, and after taking the voluntary informed consent of the pregnant women. The practices have been carried out in the massage office that was formed within the scope of the study. Electronic fetal monitoring (EFM), BPP, vital signs, fetal heart rate (FHR) evaluation have been carried out for the pregnants whose routine gestational monitoring went on during their gestational week between the 30th and 34th in the control group, and Pregnant Description Form, VAS, Prenatal Attachment Inventory-PAI, Revised Prenatal Distress Questionnaire-PDQ have been applied. In the prenatal massage therapy group, between the 30th and 34th weeks, each week for five weeks, prenatal massage therapy including a 60 minutes deep tissue and Sweden massage methods had been applied once a week. Side-Lying Positioning System that is designed specifically for the pregnant has been used during the practices. In addition, the reason why the study group consisted of pregnant women in these weeks; Perinatology specialists recommend women to experience a deep and sustainable level of relaxation for 45-60 minutes before falling asleep, especially in the last 6-8 weeks of pregnancy, in preparation for labour (Osborne et al. 2021). In line with this suggestion, since the whole body massage has been performed in the research method, a 60-minute massage (30 minutes for each lateral position) has been applied.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Aim: The study aims to determine the effect of massage during pregnancy on women and their fetuses in a university hospital in Izmir, Turkey.

Method: The study was a randomized controlled experimental trial carried out with 20-35 years-old primipara pregnant women who came to obstetrics polyclinic of a university for evaluation of their first-trimester screen test's results, had no infertility story and were not at high risk (inclusion criteria). The participants were randomly allocated to the parallel comparison groups by a central office. The sample selection process in the study has been planned to be applied according to the CONSORT criteria (Moher et al. 2010) and the permutation method with blocked randomization has been done to the records assigned from the centre that the study was applied (Kanık, Tasdelen, and Erdogan 2011). In the process of collecting data, one blinding method has been applied, and it has only been applied to data analysis. Researchers aimed to reach 30 pregnant women at the start of the study. The completion decision of the data gathering process has been determined with power analysis that is carried out by the PASS program.

The study practices have been carried out after receiving ethics committee and institution approvals after the researcher completed the prenatal massage therapy training, and after taking the voluntary informed consent of the pregnant women. The practices have been carried out in the massage office that was formed within the scope of the study. Electronic fetal monitoring (EFM), BPP, vital signs, fetal heart rate (FHR) evaluation have been carried out for the pregnants whose routine gestational monitoring went on during their gestational week between the 30th and 34th in the control group, and Pregnant Description Form, VAS, Prenatal Attachment Inventory-PAI, Revised Prenatal Distress Questionnaire-PDQ have been applied. In the prenatal massage therapy group, between the 30th and 34th weeks, each week for five weeks, prenatal massage therapy including a 60 minutes deep tissue and Sweden massage methods had been applied once a week. Side-Lying Positioning System that is designed specifically for the pregnant has been used during the practices. In addition, the reason why the study group consisted of pregnant women in these weeks; Perinatology specialists recommend women to experience a deep and sustainable level of relaxation for 45-60 minutes before falling asleep, especially in the last 6-8 weeks of pregnancy, in preparation for labour (Osborne et al. 2021). In line with this suggestion, since the whole body massage has been performed in the research method, a 60-minute massage (30 minutes for each lateral position) has been applied.

Like before the prenatal massage therapy on the first date and after the prenatal massage therapy on the last date in the control group, all the forms and measurements have been applied. Pregnant women's VAS was measured before and after the prenatal massage therapy and the evaluation of the other measured data have been held between the 31st and 33rd gestational weeks. Also, Visual Analog Patient Satisfaction Scale-VAPSS has been measured after each prenatal massage therapy for finding satisfaction levels. In the process of the study, any significant side effect related to the practices hasn't occurred. The completion decision of the data gathering process has been determined with power analysis that was carried out by PASS program. The analysis of the study data has been carried out through SPSS 16 program.

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
    • Bornova
      • İzmir, Bornova, Turkey, 35040
        • Yeliz Çakır Koçak

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

20 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • 20-35 years-old
  • Primiparous women
  • Low-risk pregnant women
  • Before the 30th week of gestation Also for the group of the prenatal massage therapy;
  • Can come 5 times for each week of gestation between 30 and 34 weeks
  • No infectious disease or skin infection on the skin,
  • No thrombosis or phlebitis
  • Single and healthy fetus
  • Written and verbally available
  • Before the 30th week of gestation
  • Accept attendance
  • Residing in the province in which the study conducted city

Exclusion Criteria:

  • Infertility story
  • High risk pregnancy
  • Live or stillbirth after 20th week of gestation
  • Abortion after the first trimester
  • History of recurrent pregnancy loss

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

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Prenatal massage therapy group
Prenatal massage therapy for prenatal attachment, physiological and psychological distress, maternal and fetal well-being.
Other: Prenatal massage therapy
Pregnant women in the intervention group had a whole body prenatal massage therapy every week between 30th and 34th gestational weeks (once a week, 5-weeks in total and 60-minutes each).Session content for the prenatal massage therapy group was created by the researcher who was 640-hours trained massaging midwife.It included 12 different massage techniques (Osborne 2015, Osborne 2021).Also, the session, which included deep tissue and Sweden massage methods, had been applied.Each session began with the pregnant woman in a side-lying position with standart special pillows (30-minutes for left, 30-minutes for right).EFM, BPP, vital signs, FHR evaluation were carried out for all participants per visiting the hospital for the study.BPP before and after prenatal massage therapy was evaluated by an obstetrician.A phone number was set for the study, and this phone number was used by the massaging midwife.The service has been provided for pregnant women to reach her whenever they want.
No Intervention: Control group
Pregnant women in the control group were interviewed twice (once a week for 30th and 34th week) by the same massaging midwife. No additional attempt was made except for filling out the forms and evaluating the biophysical profile by the obstetrician in these interviews. The massaging midwife's phone number was given to the pregnant women in both groups if they want to reach anytime. A phone number was set for the study, and this phone number was used by the massaging midwife. This service has been provided for pregnant women to reach her whenever they want.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prenatal Attachment Inventory (PAI):
Time Frame: from 30 weeks up to 34 weeks
The scale was developed by Muller (1993) and its Turkish validity-reliability study was carried out by Dereli Yılmaz and Kızılkaya Beji (2013). It is used to explain women's thoughts, feelings and situations during pregnancy and to determine the level of attachment to the baby in the prenatal period. Increased score from the scale shows that the prenatal attachment level increases. Cronbach alpha reliability coefficients ranged from 0.81 (Muller 1993) and 0.84 (Dereli Yilmaz and Kızılkaya Beji 2013). The internal reliability of this instrument was 0.87 for 30th week and 0.90 for 34th week in this sample.
from 30 weeks up to 34 weeks
Revised Prenatal Distress Questionnaire (NuPDQ):
Time Frame: from 30 weeks up to 34 weeks
The scale with different versions was developed by Yali and Lobel and the version of 17-item NuPDQ was revised by Lobel et al. (Lobel 2008; Yali and Lobel 1999). Its Turkish validity-reliability study was carried out by Yüksel et all. (Yüksel, Akın, and Durna 2011). It evaluates difficulties in pregnancy which about specific concerns and anxieties specific to the pregnancy period, such as medical problems, physical symptoms, parenting, relationships, bodily changes, birth and baby's health. The reduction of the total score of the scale shows that the prenatal distress level perceived by pregnant women decreases. Cronbach alpha reliability coefficients ranged from 0.79-0.88 (Ibrahim and Lobel 2020) and 0.85 (Yüksel et al. 2011). The internal reliability of this instrument was 0.73 for 30th week and 0.85 for 34th week in this sample.
from 30 weeks up to 34 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maternal hearth rate (MHR):
Time Frame: from 30 weeks up to 34 weeks
It was carried out for all pregnant women (control and prenatal massage therapy groups) per visiting the hospital for the study by the same midwife. The assessment were made before and after the prenatal massage therapy sessions on the first and last days of the 5-week study (two times for the control group and 10 times for the prenatal massage therapy group between the 30th and 34th gestational weeks).
from 30 weeks up to 34 weeks
Fetal hearth rate (FHR):
Time Frame: from 30 weeks up to 34 weeks
It was carried out for all pregnant women (control and prenatal massage therapy groups) per visiting the hospital for the study by the same midwife. The assessment were made before and after the prenatal massage therapy sessions on the first and last days of the 5-week study (two times for the control group and 10 times for the prenatal massage therapy group between the 30th and 34th gestational weeks).
from 30 weeks up to 34 weeks
Biophysical Profile (BPP):
Time Frame: from 30 weeks up to 34 weeks
BPP is a prenatal test used to measure the health of fetus. It has a procedure in which some variables in the USG (fetal breathing movement, fetal body movement, fetal muscle tone, amniotic fluid volume, fetal heart rate reaction) is assessed. The highest score that can be obtained from the BFP assessment is 10 (≤4: abnormal, 6: doubtful, 8-10: normal) (Alp Dal and Ertem 2016). It was carried out for all pregnant women (control and prenatal massage therapy groups) per visiting the hospital for the study by the same obstetrician. The assessment were made before and after the prenatal massage therapy sessions on the first and last days of the 5-week study (two times for the control group and 10 times for the prenatal massage therapy group between the 30th and 34th gestational weeks).
from 30 weeks up to 34 weeks
Visual Analog Scale (VAS):
Time Frame: from 30 weeks up to 34 weeks
It is developed and high reliability have been found by Hayes and Patterson. Its advantages are quickly filled out, simple, interesting, easily scored, the rater is freed from quantitative terms, it requires no master scale (Hayes and Patterson 1921). It is used to make some values that do not measure numerically. The scale is used in many different areas of health. Its main advantage is that it does not have a language and is easy to apply and consisting of a single 100 mm line (Clarke 1964). Cline et al. (1992) found that the vertical use of it is better understood (Cline et al. 1992). The mean value obtained for individuals in the general assessment is taken. Turkish validity and reliability study conducted by Eti Aslan and it is quite reliable in literate group (Eti Aslan 2004). Evaluation was performed over vertical 100 mm measurement in the study.
from 30 weeks up to 34 weeks
Visual Analog Patient Satisfaction Scale-VAPSS:
Time Frame: from 30 weeks up to 34 weeks
Kılınçer ve Zileli (2006) combined two scales features (Visual Analog Pain Scale and Wong-Baker Scale) and arranged VAPSS. It is a measurement tool that can be applied for individuals and all ages also all culture levels. They reported that the scale can use in pregnant women (Kılınçer and Zileli 2006). Evaluation was performed over vertical 100 mm measurement in the study.
from 30 weeks up to 34 weeks

Collaborators and Investigators

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

Sponsor

Ege University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

October 24, 2016

Primary Completion (Actual)

August 8, 2017

Study Completion (Actual)

November 8, 2017

Study Registration Dates

First Submitted

May 18, 2021

First Submitted That Met QC Criteria

August 10, 2021

First Posted (Actual)

August 16, 2021

Study Record Updates

Last Update Posted (Actual)

August 16, 2021

Last Update Submitted That Met QC Criteria

August 10, 2021

Last Verified

August 1, 2021

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • Yeliz Çakır Koçak
  • 16-ASYO-017 (Other Grant/Funding Number: EGE UNIVERSITY)

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.

Clinical Trials on Pregnancy Related

Clinical Trials on Prenatal massage therapy

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Netherlands

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

3
Subscribe