Actively Recruiting
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
Eligibility Criteria
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
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
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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