The Effect of Conservative Interventions on the Signs and Symptoms of Diastasis Recti
- Conditions
- Diastasis Recti And Weakness Of The Linea Alba
- Interventions
- Other: Exercise therapyOther: Abdominal binding
- Registration Number
- NCT02268110
- Lead Sponsor
- Queen's University
- Brief Summary
The purpose of this study is to determine the effect of two different physiotherapeutic interventions (exercise therapy and/or abdominal binding) on the signs and symptoms of diastasis recti in post-partum women.
- Detailed Description
This study is investigating the effect of exercise therapy and/or abdominal binding on inter-rectus distance, abdominal muscle strength and endurance, lumbopelvic dysfunction, urogynecological complaints, perceived function, and body image in post-partum women with diastasis recti
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 32
- 18 to 35 years old
- given birth to their first child, vaginally, in the last three to four weeks
- inter-rectus distance of two finger widths of greater on palpation during head lift
- history of persistent pain with intercourse prior to pregnancy
- diagnosed with neurological impairments affecting the central nervous system or sacral nerves
- diagnosed with connective tissue disorders
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Exercise therapy and Abdominal Binding Abdominal binding Participants will attend 12 sessions with a physiotherapist, and receive an abdominal binder Exercise therapy and Abdominal Binding Exercise therapy Participants will attend 12 sessions with a physiotherapist, and receive an abdominal binder Supervised exercise therapy Exercise therapy Participants will receive 12 sessions with a physiotherapist where they will receive instructions on body mechanics, and be given a progressive abdominal exercise program Abdominal binding Abdominal binding Participants will be fitted for an abdominal binder and asked to wear it for a period of 12 weeks.
- Primary Outcome Measures
Name Time Method Change in Inter-Rectus Distance baseline, 12 weeks post intervention, 9 months post intervention Measured using ultrasound imaging
- Secondary Outcome Measures
Name Time Method Change in Lumbopelvic dysfunction baseline, 12 weeks post intervention, 9 months post intervention measured using Modified Oswestry Questionnaire
Change in Abdominal Strength and Endurance baseline, 12 weeks post intervention, 9 months post intervention measured using clinical tests and hand-held dynamometry
Change in Body image baseline, 12 weeks post intervention, 9 months post intervention measured using the Multidimensional Body-Self Relations Questionnaire
Change in Severity of Lumbopelvic and/or Abdominal Pain baseline, 12 weeks post intervention, 9 months post intervention Visual Analog Scale
Change in Urogynecological Complaints baseline, 12 weeks post intervention, 9 months post intervention measured using the Pelvic Floor Distress Inventory
Change in Perceived Function baseline, 12 weeks post intervention, 9 months post intervention Inventory of Functional Status After Childbirth Questionnaire
Trial Locations
- Locations (1)
Rehabilitation Sciences Institute
🇨🇦Toronto, Ontario, Canada