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RecruitingNCT07902947Updated Oct 29, 2026

Pain Neuroscience-Based Education for Labor Pain in Pregnant Women

An interventional study of Impact of Education in Labor Pain and Anxiety, sponsored by Bilecik Seyh Edebali Universitesi. Recruiting at 3 sites in Turkey (Türkiye). Open to female participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-29.

Sponsored by Bilecik Seyh Edebali Universitesi · Not applicable, Interventional, and Screening

From the registry’s dates

  • Started Sep 2026; still recruiting 1 month later.
Updated Oct 29, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
Female
01

Study summary

Fear of labor pain and negative cognitive patterns are among the key psychological determinants that influence the childbirth experience. In particular, pain catastrophizing can lead an individual to interpret their pain experience as more threatening and difficult to manage than it actually is. This study aims to have a positive impact on an individual's pain experience.

Read the detailed description

Fear of childbirth and negative cognitive patterns are significant psychological determinants influencing the childbirth experience. In particular, pain catastrophizing can lead individuals to interpret the pain experience as more threatening and difficult to manage than it actually is. Studies indicate that high levels of pain catastrophizing are associated with the experience of labor pain, emotional distress, and negative expectations regarding childbirth (7). Similarly, recent systematic reviews evaluating non-pharmacological interventions aimed at reducing fear of childbirth report that education-based and psychoeducational approaches show promise in alleviating this fear (8).

However, educational programs for pregnant women often focus primarily on the physiological processes of childbirth, breastfeeding, and newborn care, while addressing the neurobiological mechanisms of labor pain, cognitive processes influencing pain perception, and pain-coping strategies to a limited extent. Furthermore, the participant's active role may be restricted in traditional educational models. The "flipped learning" model, which has become increasingly prevalent in health education in recent years, stands out as an approach that enables participants to access digital materials beforehand and engage actively during face-to-face sessions. It is believed that this model can enhance the retention of learning and support the individual's active participation in the process.

In this context, it is important to investigate the effects of a web-based "flipped" pain neuroscience education program-administered to pregnant women attending prenatal classes-on fear of childbirth and pain catastrophizing. Given the limited number of studies in the literature examining the effectiveness of pain neuroscience-based education regarding labor pain during pregnancy-particularly those utilizing the flipped learning model-it is anticipated that this research will contribute to the literature.

02

Conditions studied

  • Labor Pain and Anxiety

Keywords

  • Labor pain
  • Flipped learning
  • Pregnant women
03

In context

Labor Pain

423 studies on the registry are indexed under Labor Pain; 74 are open to participants now.

This study's planned enrollment of 60 is below the median of 100 across 347 interventional studies indexed under Labor Pain.

Browse Labor Pain studies →

Lead sponsor

Bilecik Seyh Edebali Universitesi is the lead sponsor of 62 studies on the registry; 27 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Pregnant Women

Exclusion criteria

Exclusion Criteria:

  • I do not wish to participate in the study
05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    The Effect of Flipped Learning on Labor Pain

    Pre-training, post-training, pre-test, post-test

    Other: Impact of Education

  • Experimental
    Pain Level

    Presentation of pain in patients

    Other: Impact of Education

Interventions

  • OtherImpact of Education

    The Effect of Flipped Learning on Labor Pain

06

What researchers measure

Primary outcomes

  1. It will be assessed using the WIJMA Delivery Expectancy Scale.

    Pain Level

    Time frame: 6 weeks

07

Study locations

3 of 3 sites recruiting
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Sep 2026 to primary completion in Oct 2026, 1 month.

Of 191 non-industry interventional studies with no phase under Labor Pain, half reached primary completion within 9 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 14. This study's 1 month is below that.

Counting every sponsor, half of 193 studies reached it within 9 months; a quarter within 5 and three quarters within 14.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 20, 2026
First posted
Oct 29, 2026
StartActual
Sep 17, 2026
Primary completionActual
Oct 19, 2026
CompletionEst.
Nov 2026
Last update
Oct 29, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 29, 2026
Show all 1 update
  1. Oct 29, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07902947
Lead sponsor
Bilecik Seyh Edebali Universitesi
Responsible party
Sponsor
First posted
Oct 29, 2026
Start date
Sep 17, 2026
Primary completion
Oct 19, 2026
Completion
Nov 2026 (estimated)
Last update
Oct 29, 2026

Study contacts

Aysun Acun, Ph.D.
Contact
aysun.acun@bilecik.edu.tr
+905072104506
Aysel Çınar, Dr.
Contact
aysel.sayhan@bilecik.edu.tr
+902282141121
Aysun Acun, Ph.D.
study director · Bilecik Seyh Edebali Universitesi

Oversight

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

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