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The Effect of Conservative Interventions on the Signs and Symptoms of Diastasis Recti

Not Applicable
Completed
Conditions
Diastasis Recti And Weakness Of The Linea Alba
Interventions
Other: Exercise therapy
Other: 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
Inclusion Criteria
  • 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
Exclusion Criteria
  • 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
GroupInterventionDescription
Exercise therapy and Abdominal BindingAbdominal bindingParticipants will attend 12 sessions with a physiotherapist, and receive an abdominal binder
Exercise therapy and Abdominal BindingExercise therapyParticipants will attend 12 sessions with a physiotherapist, and receive an abdominal binder
Supervised exercise therapyExercise therapyParticipants will receive 12 sessions with a physiotherapist where they will receive instructions on body mechanics, and be given a progressive abdominal exercise program
Abdominal bindingAbdominal bindingParticipants will be fitted for an abdominal binder and asked to wear it for a period of 12 weeks.
Primary Outcome Measures
NameTimeMethod
Change in Inter-Rectus Distancebaseline, 12 weeks post intervention, 9 months post intervention

Measured using ultrasound imaging

Secondary Outcome Measures
NameTimeMethod
Change in Lumbopelvic dysfunctionbaseline, 12 weeks post intervention, 9 months post intervention

measured using Modified Oswestry Questionnaire

Change in Abdominal Strength and Endurancebaseline, 12 weeks post intervention, 9 months post intervention

measured using clinical tests and hand-held dynamometry

Change in Body imagebaseline, 12 weeks post intervention, 9 months post intervention

measured using the Multidimensional Body-Self Relations Questionnaire

Change in Severity of Lumbopelvic and/or Abdominal Painbaseline, 12 weeks post intervention, 9 months post intervention

Visual Analog Scale

Change in Urogynecological Complaintsbaseline, 12 weeks post intervention, 9 months post intervention

measured using the Pelvic Floor Distress Inventory

Change in Perceived Functionbaseline, 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

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