Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
FEMALE
Healthy Volunteers
ID07471269

Effectiveness Of An Online Pain Neuroscience Education Intervention In Reducing Fear Of Childbirth Among Pregnant Women

Led by Cardenal Herrera University · Updated on 2026-04-15

400

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Fear of childbirth affects women of all ages and ranges from mild worry to severe anxiety, often linked to the perception of childbirth as unpredictable and painful. This trial evaluates an online pain neuroscience education program aimed at reducing fear of childbirth by teaching the neurobiological mechanisms behind pain. The study compares this approach to standard prenatal education to understand its impact on anxiety and confidence in pregnant women. Participants are randomly assigned to one of two groups. The intervention group receives 12 audiovisual lessons of pain neuroscience education adapted specifically for pregnant women, each lasting 10 to 15 minutes. These lessons focus on reshaping beliefs about pain, explaining its biological and protective role, and offering techniques to reduce fear of movement. The comparison group receives 12 sessions of standard prenatal education covering general pregnancy information and specific advice for pregnancy-related lumbopelvic pain, each session lasting about 10 minutes. During the study, pregnant women will complete assessments measuring fear of childbirth, pain catastrophizing, anxiety, and depression after 4 weeks. The study involves monitoring these psychological outcomes to evaluate the effect of the educational programs. Participation includes completing educational sessions online and providing feedback through questionnaires. The trial is expected to run until September 2026, with a focus on improving emotional well-being during pregnancy.

CONDITIONS

Brief Title

Online Pain Neuroscience Education For Fear Of Childbirth.

Who Can Participate

Age: 18Years - 50Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women over 18 years of age
  • Primiparous or multiparous women
  • At the beginning of the third trimester of pregnancy
Not Eligible

You will not qualify if you...

  • Multiple pregnancies
  • Previous spinal surgery
  • Psychiatric disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Approximately 4 weeks

Participants receive 12 educational sessions of either pain neuroscience education or standard prenatal education, each lasting about 10 to 15 minutes, delivered online in audiovisual format.

12 sessions delivered online

Trial Site Locations

Total: 1 location

1

University Cardenal Herrera

Alfara del Patriarca, Valencia, Spain, 46115

Actively Recruiting

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Research Team

J

JF Lisón, Dr

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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