Comparing two therapies for neck pain in breastfeeding mothers
Effectiveness of High Tone Power Therapy Versus Interferential Current Therapy in Mothers With Breastfeeding-Related Neck Pain
This study tests which therapy, high tone power therapy or interferential current therapy, works better to relieve neck pain in mothers who are breastfeeding.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 45 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | Female |
| Sponsor | October 6 University Academic / other |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06573515 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of high tone power therapy versus interferential current therapy in alleviating neck pain experienced by breastfeeding mothers. The study focuses on mothers who are exclusively breastfeeding and examines how these therapies can improve cervical spine mobility and reduce pain. Participants will receive either of the two therapies to determine which is more effective in treating musculoskeletal issues related to breastfeeding. The trial aims to provide insights into better pain management strategies for new mothers.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy, first-time breastfeeding mothers aged 18-35 with a normal body mass index.
Not a fit: Patients with pre-existing orthopedic or neurological conditions, cesarean deliveries, or chronic diseases may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide effective pain relief options for breastfeeding mothers, enhancing their overall well-being and ability to care for their infants.
How similar studies have performed: Previous studies have shown positive outcomes with similar therapeutic approaches for musculoskeletal pain, suggesting potential success for this trial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All mothers are medically stable. * All mothers are primiparous and currently breastfeed their infants. * All mothers will be exclusive breastfeeding mothers. * Their ages will be 18-35 years old. * Their body mass index will be 18.5 to 24.9 kg/m2. * All mothers will provide an informed consent form agreeing to participate and publication of the study results. Exclusion Criteria: * Mothers who were pregnant and nursing with known orthopedic and neurological conditions of the spine, upper limbs and shoulder regions prior to breastfeeding. * Mothers had cesarean delivery. * Mothers with cerebrovascular problems, or any disorder affect the goal of the study. * Mothers with preterm babies, low-birth weight babies, intrauterine growth restriction, with chronic diseases like cancer, human immuno-deficiency virus (HIV), tuberculosis and with postpartum complications like postpartum hemorrhage and eclampsia.
Where this trial is running
Cairo
- Heba — Cairo, Egypt (Recruiting)
Study contacts
- Study coordinator: Heba ahmed haridy, doctoral
- Email: Heba.Ahmed.PT@o6u.edu.eg
- Phone: 01117671712
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.