About this trial
A randomised controlled trial with the aim of analysing the effectiveness of a training program intended to prevent symptoms related to DRAM in the postpartum period.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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
Disqualifiers
Ongoing pregnancy
Age <18 years or >50 years
< 3 months or >12 months post partum
History of neurologic, musculoskeletal or psychiatric disorders
Trial design
Parallel
Treatments tested in this trial
Naprapathy training
BehavioralActive training aimed at strengthening the abdominal muscles
Control group
Other interventionNo change of daily routines in regard to training
Treatment groups
Trial outcomes
Primary outcomes
Abdominal Trunk Function
Abdominal Trunk Function assessed with the Abdominal Trunk Function Protocol (ATFP). Six separate subscales.
Secondary outcomes
Disability
Disability rated with the Disability Rating index (DRI). Rates ranging from 0 to 1200, where high ratings indicate worse outcome.
Urinary Incontinence
Urinary incontinence rated with UDI-6 (urinary distress inventory). Rates ranging from 0 to 18, where high rates indicate worse outcome.
Health-related Quality of Life
Quality of Life rated with EQ-5D
Width of the diastasis
Width measured with ultrasound
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Karolinska Institutet
Lead sponsor
Hela Kvinnans Klinik
Collaborator