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Clinical Trials/NCT02268110
NCT02268110CompletedNot 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 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

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

Study 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

Arms & Interventions

Supervised exercise therapy

Experimental

Participants will receive 12 sessions with a physiotherapist where they will receive instructions on body mechanics, and be given a progressive abdominal exercise program

Intervention: Exercise therapy (Other)

Abdominal binding

Experimental

Participants will be fitted for an abdominal binder and asked to wear it for a period of 12 weeks.

Intervention: Abdominal binding (Other)

Exercise therapy and Abdominal Binding

Experimental

Participants will attend 12 sessions with a physiotherapist, and receive an abdominal binder

Intervention: Exercise therapy (Other)

Exercise therapy and Abdominal Binding

Experimental

Participants will attend 12 sessions with a physiotherapist, and receive an abdominal binder

Intervention: Abdominal binding (Other)

Control

No Intervention

Participants will not receive an intervention during the study period

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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