- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07371039
Sacral Pressure During Labor: Effects on Pain and Maternal Satisfaction
January 22, 2026 updated by: Ayşegül Muslu, Izmir Kavram Vocational School
Effects of a Nurse-Led Sacral Pressure Intervention During Labor on Pain Perception and Maternal Satisfaction: A Randomized Controlled Trial
The study will be conducted with pregnant women in the active and transitional phases of labor.
In the intervention group, sacral pressure will be applied during contractions, while the control group will receive routine clinical care.
Perceived labor pain and maternal satisfaction will be assessed throughout the labor process
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
60
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 Contact
- Name: AYSEGÜL MUSLU, Phd
- Phone Number: +90444 9 134
- Email: aysegulmuslu777@gmail.com
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Aged 18 years or older
- Singleton pregnancy
- Cephalic (vertex) presentation
- Gestational age between 37 and 42 weeks
Exclusion Criteria
- Illiterate in Turkish
- Presence of chronic disease(s)
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: Prevention
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Sacral massage applied to the S4-S5 bones
Pressure will be applied to minimize the mother's pain in order to facilitate contractions.
|
Pressure application using the metacarpal bone of one hand on the S4-S5 bones was planned.
|
|
No Intervention: routine clinical practice
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The VAS Pain Scale
Time Frame: Average: 1 year
|
Average: 1 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The Intrapartum Period Satisfaction Form
Time Frame: Average: 1 year
|
Average: 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: AYSEGÜL MUSLU, izmir kavram vocation
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 (Estimated)
February 1, 2026
Primary Completion (Estimated)
March 15, 2026
Study Completion (Estimated)
April 20, 2026
Study Registration Dates
First Submitted
January 14, 2026
First Submitted That Met QC Criteria
January 22, 2026
First Posted (Actual)
January 27, 2026
Study Record Updates
Last Update Posted (Actual)
January 27, 2026
Last Update Submitted That Met QC Criteria
January 22, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E1881
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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