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

Recruiting N/A Interventional Study
Low Back Pain Lumbopelvic Pain Pelvic Girdle Pain
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 40
Sex
Female
Study type
Interventional
Purpose
Diagnostic
Participants needed
211 (estimated)
Sponsor
Hasselt University · Other
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About This Trial
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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Informed consent to participate * 18-40 years old * Pregnant * Singleton pregnancy (confirmed through ultrasound) * No current PLPP * Dutch- or English-speaking Exclusion Criteria: * Pregnant for more than 16 weeks * Currently experiencing PLPP, or having had PLPP during the…
Contacts

Lotte Janssens, Prof, PhD

+32 474 43 56 39

lotte.janssens@uhasselt.be

CONTACT

Inge Geraerts, Prof, PhD

+32 16 32 91 20

inge.geraerts@kuleuven.be

CONTACT