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:
2025-12-25 @ 4:41 AM
Ignite Modification Date:
2025-12-25 @ 4:41 AM
NCT ID:
NCT04981418
Eligibility Criteria:
Inclusion Criteria:
* Women aged greater than or equal to 18
* Able and willing to provide informed consent
* Self reported Persistent pelvic girdle pain (PGP) (≥3 months post partum)
* Self reported severe PGP (causing walking or stair climbing to be bothersome)
* Diagnosed with PGP in line with European guidelines
* PGP must have started or been aggravated during pregnancy, as determined by self report
Exclusion Criteria:
* known allergy to lycra
* age \< 18
* currently pregnant
* PGP for \> 2 years post partum
* Self reported history of pathologies causative of lumbo pelvic pain(e.g. Infection, trauma, cancer)
* Participating in concurrent interventional research which may over-burden the patient or confound data collection
* There are no special arrangements made for participants who are unable to adequately understand verbal and/or written English. There is no intention to exclude patients, therefore, if they have regular access to a friend or family member who is able to translate for them they would be able to participate
* Participants who lack capacity to provide informed consent
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT04981418
Study Brief:
Protocol Section:
NCT04981418