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 @ 11:44 PM
Ignite Modification Date:
2025-12-24 @ 11:44 PM
NCT ID:
NCT07292051
Eligibility Criteria:
Inclusion Criteria:
* Patients will be eligible for the study if they met all the following criteria:
1. Are between 3 and 12 months postpartum.
2. Are aged between 20 and 35 years.
3. Have a body mass index (BMI) \< 30 kg/m².
4. Reported experiencing pelvic girdle pain-defined as pain localized between the posterior iliac crest and the gluteal fold, particularly in the vicinity of the sacroiliac joints-that either began during pregnancy or persisted after delivery .
5. Presented with a positive Active Straight Leg Raise (ASLR) test.
6. Showed positive findings in at least two of the following six pelvic pain provocation tests:
* Posterior Pelvic Pain Provocation (P4/Thigh Thrust) Test
* Patrick's (FABER) Test
* Long Dorsal Sacral Ligament Test
* Pelvic Compression Test
* Pelvic Distraction (Separation) Test
* Sacral Thrust Test
Exclusion Criteria:
* -Patients will be excluded if they have any of the following:
1. If they were Pregnant
2. Known causes of pelvic girdle pain, such as fractures and rheumatism
3. Undergone lumbar or pelvic surgery in the past
4. Current neurological symptoms and signs in lower extremities such as lumbar radiculopathy and myelopathy
5. Cancer
6. Cardiovascular disease
7. Experience with structured and supervised core or trunk exercise training programs
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
35 Years
Study:
NCT07292051
Study Brief:
Protocol Section:
NCT07292051