Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
FEMALE
NCT06785909

Proprioceptive, Fear-related and Inflammatory Factors in the Persistence of Pregnancy-related Lumbopelvic Pain.

Led by Hasselt University · Updated on 2025-12-02

211

Participants Needed

2

Research Sites

199 weeks

Total Duration

On this page

Sponsors

H

Hasselt University

Lead Sponsor

K

KU Leuven

Collaborating Sponsor

AI-Summary

What this Trial Is About

Pregnancy-related lumbopelvic pain (PLPP) affects 50-90% of pregnant women and is often dismissed as a normal part of pregnancy. However, the long-term consequences can be dramatic. Up to 21% of women with PLPP still have pain three years postpartum, and 10% experience disability, poorer quality of life, and lower ability to work 11 years after delivery. Because the multifactorial etiology of PLPP is unclear, prevention and treatment fall short. Previous studies on the causes of PLPP focused on impairments in motor output but ignored that impairments in sensory input (e.g., proprioception, the primary expertise of our research group) often precede motor output problems. Moreover, though psychological factors such as fear (of movement) are known to affect PLPP, their predictive role in PLPP remains understudied. Finally, the role of systemic inflammation in PLPP has yet to be examined, despite recent studies demonstrating its role in the chronification of lumbopelvic pain in the general population. This prospective cohort study aims to identify new modifiable predictors for the onset of PLPP during pregnancy and its persistence postpartum. The investigators will compare sensory (proprioception, body perception), fear-related, and inflammatory factors between women with and without PLPP and determine their predictive role in the onset and persistence of PLPP. The results will increase our understanding of the multifactorial etiology of PLPP and help optimize prevention and treatment.

CONDITIONS

Official Title

Proprioceptive, Fear-related and Inflammatory Factors in the Persistence of Pregnancy-related Lumbopelvic Pain.

Who Can Participate

Age: 18Years - 40Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Provided informed consent to participate
  • Aged 18 to 40 years
  • Currently pregnant
  • Have a singleton pregnancy confirmed by ultrasound
  • Do not currently have pregnancy-related lumbopelvic pain (PLPP)
  • Able to speak Dutch or English
Not Eligible

You will not qualify if you...

  • Pregnant for more than 16 weeks at the time of enrollment
  • Currently experiencing PLPP or had PLPP during the current pregnancy
  • History of surgery or major trauma to the spine or pelvis
  • History of major trauma or surgery to lower limbs more than 2 years ago with ongoing symptoms
  • History of major trauma or surgery to lower limbs less than 2 years ago
  • Specific vestibular or balance disorders
  • Use of medication that affects balance (e.g., ototoxic or centrally-acting drugs)
  • Diagnosed with or treated for rheumatic conditions or taking related medication
  • History of neurological disorders (e.g., neuropathy)
  • Uncorrected vision problems
  • Recent ankle problems (e.g., sprain within last 3 weeks)
  • On absolute or relative bed rest due to pregnancy complications
  • History of inflammatory, autoimmune diseases, hypothyroidism, or cancer
  • Diagnosed with or treated for psychiatric disorders (e.g., psychotic disorder)

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Hasselt University

Hasselt, Belgium

Actively Recruiting

2

KU Leuven

Leuven, Belgium

Actively Recruiting

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Research Team

L

Lotte Janssens, Prof, PhD

CONTACT

I

Inge Geraerts, Prof, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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