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Long-Term Effectiveness of Pain Neuroscience Education in Women With Genito-Pelvic Pain/Penetration Disorder.

Long-Term Outcomes at Five Years Following Pain Neuroscience Education in Women With Genito-Pelvic Pain/Penetration Disorder: Observational Follow-Up of a Randomized Controlled Trial.

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07463066
Enrollment
69
Registered
2026-03-10
Start date
2026-04-01
Completion date
2026-04-30
Last updated
2026-03-13

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

Conditions

Genito-Pelvic Pain/Penetration Disorder

Keywords

Pain, Pelvic pain, Dysfunction sexual

Brief summary

The goal of this observational follow-up study is to learn whether the benefits of Pain Neuroscience Education are maintained five years after the original intervention in women previously diagnosed with Genito-Pelvic Pain/Penetration Disorder who participated in a randomized controlled trial. The main questions it aims to answer are: Are improvements in pain intensity maintained five years after the intervention? Are improvements in sexual function and pain-related disability sustained over time? Researchers will compare participants according to the treatment group to which they were originally assigned in the randomized controlled trial to evaluate long-term differences in outcomes. Participants will: Complete questionnaires assessing pain intensity, sexual function, and pain-related outcomes. Undergo follow-up assessments similar to those performed during the original study.

Detailed description

Genito-Pelvic Pain/Penetration Disorder is a chronic pain condition that significantly affects physical, emotional, and sexual well-being. Women experiencing persistent pelvic pain frequently report difficulties related not only to pain intensity but also to sexual function, fear of movement or penetration, and reduced quality of life. Despite its high impact, conservative treatment approaches remain underutilized, and long-term management strategies are still being explored. Pain Neuroscience Education (PNE) has emerged over the last decade as a therapeutic approach aimed at helping patients understand the neurophysiological mechanisms underlying persistent pain. By reconceptualizing pain as a multifactorial and modifiable process rather than solely a marker of tissue damage, PNE seeks to reduce fear, maladaptive beliefs, and pain-related disability. Growing evidence supports its short- and medium-term effectiveness in various chronic pain populations. Five years ago, a multi-centered randomized controlled trial evaluated the effectiveness of a structured Pain Neuroscience Education program in women diagnosed with Genito-Pelvic Pain/Penetration Disorder. The intervention was delivered through different educational modalities and demonstrated clinically relevant improvements following treatment. However, evidence regarding the durability of these effects over extended periods remains limited. Long-term follow-up studies are essential to determine whether educational interventions targeting pain processing produce sustained changes in pain perception, functional outcomes, and overall well-being. The present study is designed as a long-term observational follow-up of the original randomized controlled trial cohort. No new intervention will be administered. Instead, participants who were previously enrolled will be reassessed five years after completion of the initial intervention in order to evaluate the persistence of treatment-related changes over time. This study will contribute to understanding the long-term trajectory of women treated with Pain Neuroscience Education for persistent pelvic pain and will help clarify the potential role of educational strategies as durable components of conservative pain management.

Interventions

OTHERIn person workshops

Several in person workshops given by a researcher

Access to a website containing the educational program

Sponsors

University of Valencia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- Patients over 18 years-old suffering from dyspareunia for more than 3 months

Exclusion criteria

\- Patients suffering from a previous medical condition that explains logically the presence of pain

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue ScaleBaselinePain intensity assessment instrument. Minimum value 0, maximum value 10. Higher scores mean worse outcome

Secondary

MeasureTime frameDescription
Pain Catastrophizing ScaleBaselineInstrument developed quantify an individual's pain experience. Minimum value 0, maximum value 52. Higher scores mean worse outcome.
Survey of Pain AttitudesBaselineInstrument to understand the pain-related beliefs of your chronic pain patients. Minimum value 0, maximum value 285. Higher scores mean better results.
Female Sexual Function IndexBaselineInventory designed to assess female sexual function. Minimum value 2, maximum value 36. Higher scores mean better functioning.

Countries

Spain

Contacts

CONTACTBorja Perez-Dominguez, PhD.
f.borja.perez@uv.es+34 697464680

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026