Training program to prevent Diastasis Recti after pregnancy
Randomised Controlled Trial to Assess the Benefit of Naprapathy Training for Preventing Problems from Rectus Abdominis Diastasis
This study tests a special training program to see if it can help new moms prevent problems related to diastasis recti, which is a separation of abdominal muscles after pregnancy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 70 (estimated) |
| Ages | 18 Years to 50 Years |
| Sex | Female |
| Sponsor | Karolinska Institutet Academic / other |
| Locations | 1 site (Stockholm) |
| Trial ID | NCT04652830 on ClinicalTrials.gov |
What this trial studies
This randomized controlled trial aims to evaluate the effectiveness of a specific naprapathy training program designed to prevent symptoms related to diastasis recti in postpartum women. The study will involve women who are 3-12 months postpartum and have a diastasis of the rectus abdominis muscles greater than 3 cm. Participants will be randomly assigned to either the training program or a control group, and the study will assess changes in abdominal function and anatomy over a three-month follow-up period. The research seeks to fill the gap in understanding how diastasis recti affects trunk stability and back pain.
Who should consider this trial
Good fit: Ideal candidates are women who are 3-12 months postpartum with a diastasis recti greater than 3 cm.
Not a fit: Patients who are currently pregnant or have a history of significant neurological, musculoskeletal, or psychiatric disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve abdominal strength and reduce back pain in postpartum women with diastasis recti.
How similar studies have performed: While there is limited research on the effectiveness of training programs for preventing diastasis recti, this approach is novel and aims to address a significant gap in existing literature.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Uni- and multiparous women 3-12 months postpartum * Ability to understand Swedish language * Ability participate in a three months follow-up program * Diastasis of the rectus abdominis muscles \> 3 cm Exclusion Criteria: * Ongoing pregnancy * Age \<18 years or \>50 years * \< 3 months or \>12 months post partum * History of neurologic, musculoskeletal or psychiatric disorders * Interrectal diastasis \< 3 cm
Where this trial is running
Stockholm
- Hela Kvinnans Klinik — Stockholm, Sweden (Recruiting)
Study contacts
- Principal investigator: Gabriel Sandblom, Ass Prof — Karolinska Institutet
- Study coordinator: Katarina Woxnerud, Naprapath
- Email: katarina@woxnerud.se
- Phone: +46 702694900
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.