CClinicalTrials.gg
CompletedNCT07151144Updated Jan 2, 2026

Effects of Massage and Shower on Birth Experience and Breastfeeding

An interventional study of Massage and Shower in Pregnancy and Delivery Care, sponsored by Sakarya University. Completed at 1 site in Turkey (Türkiye). Open to female participants aged 19 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-02.

Sponsored by Sakarya University · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
19 Years to 45 Years
Sex
Female
01

Study summary

Study Design This study is a quasi-experimental research designed to examine the effects of massage and warm shower-used as non-pharmacological methods during labor-on birth satisfaction, maternal comfort, and breastfeeding success.

tudy Population

The study was conducted in the delivery unit of a public hospital in Turkey in 2025. The sample consisted of women who were experiencing their first pregnancy and giving birth for the first time. Inclusion criteria were as follows:

Between 37 and 42 weeks of gestation,

Low-risk, singleton pregnancies,

Planned for vaginal delivery,

No significant obstetric complications during pregnancy,

Voluntarily agreed to participate in the study.

A total of 120 participants were randomly assigned into three groups:

Massage Group (n=430): Received massage during labor.

Shower Group (n=40): Took a warm shower during labor.

Control Group (n=40): Received routine standard hospital care without any additional intervention.

Data Collection Tools

Data were collected using the following instruments:

Personal Information Form

Birth Satisfaction Scale

Birth Comfort Scale

Breastfeeding Success Scale Intervention Massage Group: During the active phase of labor (cervical dilation of 4-7 cm), participants received 15-minute sessions of light-pressure massage to the lower back, sacrum, and lumbar area at regular intervals.

Shower Group: During the same phase, participants were assisted to take a warm shower for approximately 20 minutes.

Control Group: Received routine intrapartum care with no additional non-pharmacological intervention

Read the detailed description

Before the intervention (baseline during early labor),

Immediately after birth (for comfort and satisfaction),

Within the first 2 hours postpartum (for breastfeeding success).

02

Conditions studied

  • Pregnancy
  • Delivery Care
03

In context

Lead sponsor

Sakarya University is the lead sponsor of 178 studies on the registry; 48 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

Between 37 and 42 weeks of gestation,

Low-risk, singleton pregnancies,

Planned for vaginal delivery,

No significant obstetric complications during pregnancy,

Voluntarily agreed to participate in the study.

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
120 participants (actual)

Study arms

  • Experimental
    intervention group

    Massage and Showe

    Other: Massage · Other: Shower

  • No intervention
    Control group

    Control group

Interventions

  • OtherMassage

    During the active phase of labor (cervical dilation of 4-7 cm), participants received 15-minute sessions of light-pressure massage to the lower back, sacrum, and lumbar area at regular intervals.

  • OtherShower

    During the same phase, participants were assisted to take a warm shower for approximately 20 minutes.

06

What researchers measure

Primary outcomes

  1. Birth Satisfaction

    Evaluated using the Birth Satisfaction Scale (BSS), which measures a mother's satisfaction with her labor and delivery experience (The scale is a 30-item Likert-type scale. The lowest possible score is 30, and the highest is 150. A higher score indicates higher birth satisfaction.). The scale includes multiple dimensions such as quality of care, personal attributes, and stress experienced during labor. 25 September, 2025-15 December, 2025

    Time frame: up to 3 months

  2. Maternal Comfort

    Maternal Comfort: Assessed through the Birth Comfort Scale, which evaluates physical, emotional, and environmental aspects of comfort experienced by the mother during labor (The scale is a 34-item Likert-type scale. The lowest possible score is 34, and the highest is 170. A higher score indicates higher postpartum comfort). 25 September, 2025-15 December, 2025

    Time frame: up to 3 months

  3. Breastfeeding Success:

    Measured within the first hours postpartum using the LATCH Breastfeeding Assessment Tool, which assesses five components: Latch, Audible swallowing, Type of nipple, Comfort (breast/nipple), and Hold (positioning).A low score indicates unsuccessful breastfeeding, while a high score indicates successful breastfeeding.

    Time frame: Within the first 2 hours postpartum

07

Study locations

1 site
  • Sakarya University
    Sakarya, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — Ethically, patient information can be shared upon reasonable request without revealing their identities for security reasons.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07151144
Lead sponsor
Sakarya University
Responsible party
öznur tiryaki (Associate Professor, Sakarya University) — Principal investigator
First posted
Sep 3, 2025
Start date
Aug 25, 2025
Primary completion
Nov 15, 2025
Completion
Dec 15, 2025
Last update
Jan 2, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

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