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.
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