The Effect of Pregnant-controlled Sacral Massage on Mothers' Labor Pain, Perception, Process and Midwives' Satisfaction

Status

Not yet recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06499402

Enrollment

112

Registered

2024-07-12

Start date

2024-07-22

Completion date

2024-09-22

Last updated

2024-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labor, Labor Pain

Brief summary

Our study aims to determine the effect of pregnant-controlled automatic sacral massage on mothers' labor pain, perception, process and midwives' satisfaction. The research was planned as a randomized controlled experimental study. A total of 112 women, 56 pregnant women in the experimental and control groups, will be included in the study. In this project, an automatic massage device will be used during the active phase (when the cervical opening is between 5-6 cm and 10 cm) and a massage device in line with the pregnancy-controlled sacral massage application protocol. Pregnant women are followed throughout the active phase of labor and indicators reflecting labor pain, progress of labor, and the health status of the mother and the baby are used with the Individual Identification Form, Visual Comparison Scale, Labor Monitoring Form, Mother's Birth Perception Scale (ADAS). The satisfaction of midwives will be evaluated with the Evaluation of Satisfaction Status of Midwives Form.

Interventions

OTHERmassage

sacral massage

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

SINGLE (Subject)

Eligibility

Sex/Gender

FEMALE

Age

18 Days to 45 Days

Healthy volunteers

Yes

Inclusion criteria

* Participating in the study voluntarily * having a cervical dilatation of 5-6 cm, * being between 38-40 weeks of pregnancy,- being a single fetus, having a cephalic presentation, * having a fetal weight between 2.5-4 kg, * having no vision-hearing problems, * having communication and cooperation skills

Exclusion criteria

* having pregnancy complications * Those who have acute inflammatory problems in soft tissues, skin or joints, burns, nerve injuries, open wounds, rheumatoid and gouty arthritis, * those who have used any non-pharmacological methods will not be admitted.

Design outcomes

Primary

Measure	Time frame	Description
stress	1 day	questionnaire, stress scale

Secondary

Measure	Time frame	Description
labor pain	1 day	pain scale, VAS

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026