Treatment for postpartum pelvic pain using physiotherapy and radiofrequency
Efficacy of Radiofrequency and the Treatment of Myofascial Pain Syndrome in Postpartum Pelvic Pain: Mixed Research Study
This study tests if combining physiotherapy with radiofrequency can help women with pelvic pain after giving birth feel better and improve their sexual function.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 74 (estimated) |
| Ages | 18 Years to 45 Years |
| Sex | Female |
| Sponsor | University of Alcala Academic / other |
| Locations | 1 site (Alcalá de Henares, Madrid) |
| Trial ID | NCT06469632 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of a physiotherapy treatment combined with radiofrequency for women experiencing pelvic pain after vaginal delivery. It will involve a randomized design with two groups, where one group receives physiotherapy focused on myofascial pain syndrome and pelvic floor muscle training, while the other group receives the same treatment with the addition of radiofrequency. The study will also explore factors influencing adherence to treatment and women's self-efficacy regarding their recovery. The goal is to reduce pain and improve sexual function in postpartum women suffering from pelvic pain.
Who should consider this trial
Good fit: Ideal candidates are primiparous women who have experienced vaginal delivery and are suffering from pelvic pain at least eight weeks postpartum.
Not a fit: Patients who have had multiple births, cesarean deliveries, or specific pelvic injuries may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could significantly alleviate pelvic pain and enhance sexual function for postpartum women.
How similar studies have performed: While there is limited data on this specific combination of treatments, similar physiotherapy approaches have shown promise in managing pelvic pain in postpartum women.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Primiparous women * Eutocic vaginal birth * Postpartum pelviperineal pain 8 weeks after birth * Intensity ≥ 4 cm in the VAS * Freely signed the Informed consent Exclusion Criteria: * Multiparous women * Instrumental delivery * Cesarean delivery * Avulsion of the levator ani muscle * Diagnosis of coccygodynia and/or coccygeal pain * Sphincter anal injury during vaginal birth * History of pelvic fractures and/or neoplasms * Pregnant women * Neurological diseases * Vaginal infection or active urinary tract, or with any * Uterine device with metallic components * Women with cognitive, auditory and/or visual limitations to understand information, respond to questionnaires, consent and/or participate in the study.
Where this trial is running
Alcalá de Henares, Madrid
- Physiotherapy in Women's Health (FPSM) Research Group. Physiotherapy Department, Faculty of Medicine and Health Sciences, University of Alcalá, Alcalá de Henares, 28805 Madrid, Spain. — Alcalá de Henares, Madrid, Spain (Recruiting)
Study contacts
- Principal investigator: Beatriz Navarro-Brazález, PhD — Physiotherapy in Women's Health (FPSM) Research Group. Physiotherapy Department, Faculty of Medicine and Health Sciences, University of Alcalá, Alcalá de Henares, 28805 Madrid, Spain.
- Study coordinator: Beatriz Navarro-Brazález, PhD
- Email: b.navarro@uah.es
- Phone: +34918854828
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.