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 @ 4:52 AM
Ignite Modification Date:
2025-12-25 @ 4:52 AM
NCT ID:
NCT07078318
Eligibility Criteria:
Inclusion Criteria:
Female participants aged between 18 and 45 years
Experiencing dyspareunia of musculoskeletal origin for at least 6 months
In a stable sexual relationship and sexually active
Willing and able to attend weekly treatment sessions for 8 weeks
Able to provide informed consent
No pelvic surgery within the last 6 months
Normal cognitive function and ability to follow instructions
Baseline FSFI score indicating sexual dysfunction (e.g., ≤ 26.55)
Exclusion Criteria:
* Presence of neurological, gynecological, or urological pathologies causing pelvic pain (e.g., endometriosis, pelvic inflammatory disease)
Pregnancy or postpartum period within the last 6 months
Diagnosed psychiatric disorders (e.g., major depression, psychosis)
Use of medications that affect autonomic nervous system function (e.g., beta-blockers, antidepressants)
History of pelvic radiation, cancer, or pelvic trauma
Participation in other rehabilitation or psychotherapy programs during the study period
Inability to tolerate manual therapy or perform breathing exercises
BMI \> 35, which may interfere with ultrasonographic assessment
Non-compliance risk, such as irregular attendance or language barriers
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT07078318
Study Brief:
Protocol Section:
NCT07078318