Skip to main content
Clinical Trials/NCT02268110
NCT02268110
Completed
Not Applicable

The Effect of Exercise Therapy and/or Abdominal Binding on Inter-rectus Distance, Abdominal Muscle Strength, Lumbopelvic and Urogynecological Complaints, Perceived Function, and Body Image in Post-partum Women With Diastasis Recti

Queen's University1 site in 1 country32 target enrollmentAugust 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diastasis Recti And Weakness Of The Linea Alba
Sponsor
Queen's University
Enrollment
32
Locations
1
Primary Endpoint
Change in Inter-Rectus Distance
Status
Completed
Last Updated
7 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
August 2014
End Date
May 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nadia Keshwani

PhD candidate

Queen's University

Eligibility Criteria

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

Outcomes

Primary Outcomes

Change in Inter-Rectus Distance

Time Frame: baseline, 12 weeks post intervention, 9 months post intervention

Measured using ultrasound imaging

Secondary Outcomes

  • Change in Lumbopelvic dysfunction(baseline, 12 weeks post intervention, 9 months post intervention)
  • Change in Abdominal Strength and Endurance(baseline, 12 weeks post intervention, 9 months post intervention)
  • Change in Body image(baseline, 12 weeks post intervention, 9 months post intervention)
  • Change in Severity of Lumbopelvic and/or Abdominal Pain(baseline, 12 weeks post intervention, 9 months post intervention)
  • Change in Urogynecological Complaints(baseline, 12 weeks post intervention, 9 months post intervention)
  • Change in Perceived Function(baseline, 12 weeks post intervention, 9 months post intervention)

Study Sites (1)

Loading locations...

Similar Trials