Phase
Condition
N/ATreatment
Assessment of postural control, body perception, psychosocial factors and inflammation
Clinical Study ID
Ages 18-40 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Informed consent to participate
18-40 years old
First pregnancy
Singleton pregnancy (confirmed through ultrasound)
No current PLPP
Dutch- or English speaking
Exclusion
Exclusion Criteria:
Pregnant for more than 16 weeks
Currently experiencing PLPP, or having had PLPP during the index pregnancy
History of surgery or major trauma to spine, pelvis or legs
Specific vestibular or balance disorders
Use of medication that could affect balance (e.g., ototoxic or centrally-actingdrugs)
Specific spinal conditions or deformities (e.g., structural scoliosis)
Rheumatic disease
(History of) a neurological disorder (e.g., neuropathy)
Problems with vision that are not corrected by glasses, contact lenses or surgicaleye correction
Hyperemesis gravidarum
Recent history of ankle problem (e.g., ankle sprain less than 3 weeks ago)
Currently having a condition that may compromise the normal course of the pregnancy (e.g., hypertension, renal disease, coagulation disorder)
Use of corticosteroids or NSAIDs
(History of) endocrine, nutritional, metabolic, inflammatory, (auto)immune,cardiovascular conditions, or cancer
Comorbidities that might influence inflammatory markers (e.g., acute illness,infection (e.g. CMV, HPV, urinary tract infection...), hypothyroidism,endometriosis)
(History of) psychiatric disorder
Study Design
Study Description
Connect with a study center
Hasselt University
Hasselt,
BelgiumActive - Recruiting
KU Leuven
Leuven,
BelgiumActive - Recruiting
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