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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 enrollmentStarted: August 2014Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
32
Locations
1
Primary Endpoint
Change in Inter-Rectus Distance

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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

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)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Nadia Keshwani

PhD candidate

Queen's University

Study Sites (1)

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