Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 8:03 PM
Ignite Modification Date:
2025-12-24 @ 8:03 PM
NCT ID:
NCT07186504
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women aged ≥18 years
* Gestational age ≤27 weeks at enrollment
* Clinically confirmed pelvic girdle pain, defined as:
* Pain localized between the posterior iliac crest and the gluteal fold, particularly around the sacroiliac joints and/or pubic symphysis, Pain intensity ≥3/10 on Visual Analog Scale (VAS), At least 3 positive clinical tests among: Posterior Pelvic Pain Provocation (P4) test, Patrick's FABER, Menell's test, Active Straight Leg Raise (ASLR), and palpation of long dorsal sacroiliac ligament or symphysis pubis
* Ability to understand and provide written informed consent
Exclusion Criteria:
* Isolated low back pain without pelvic involvement
* Contraindications to exercise during pregnancy (e.g., severe preeclampsia, placenta previa after 26 weeks, risk of preterm labor, ruptured membranes, significant cardiac or pulmonary disease)
* Neurological, rheumatologic, or orthopedic conditions that may interfere with participation
* Insufficient French language proficiency to understand questionnaires and instructions
* Participation in another interventional study that could affect outcomes
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT07186504
Study Brief:
Protocol Section:
NCT07186504