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 @ 5:43 PM
Ignite Modification Date:
2025-12-24 @ 5:43 PM
NCT ID:
NCT07037368
Eligibility Criteria:
Inclusion Criteria:
* Postpartum females aged 20-40 years
* Females who delivered via vaginal delivery or cesarean section
* 6 weeks to 6 months postpartum period
* Willingness to participate and provide informed consent
Exclusion Criteria:
* Females with a history of pelvic or spinal surgery prior to pregnancy
* Known cases of pre-existing musculoskeletal disorders (e.g., scoliosis, chronic back pain)
* Multiple pregnancies (twins or more) in the current or previous delivery
* Postpartum complications unrelated to delivery mode (e.g., sepsis, trauma)
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT07037368
Study Brief:
Protocol Section:
NCT07037368