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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02268110
Other study ID # REH-566-13
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2014
Est. completion date May 2018

Study information

Verified date September 2018
Source Queen's University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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 information / eligibility

Status Completed
Enrollment 32
Est. completion date May 2018
Est. primary completion date August 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 35 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Other:
Exercise therapy
Supervised exercise therapy with a 12 week progressive abdominal exercise home program for
Abdominal binding
Wearing an abdominal binder for 12 weeks

Locations

Country Name City State
Canada Rehabilitation Sciences Institute Toronto Ontario

Sponsors (2)

Lead Sponsor Collaborator
Queen's University University of Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Inter-Rectus Distance Measured using ultrasound imaging baseline, 12 weeks post intervention, 9 months post intervention
Secondary Change in Abdominal Strength and Endurance measured using clinical tests and hand-held dynamometry baseline, 12 weeks post intervention, 9 months post intervention
Secondary Change in Body image measured using the Multidimensional Body-Self Relations Questionnaire baseline, 12 weeks post intervention, 9 months post intervention
Secondary Change in Lumbopelvic dysfunction measured using Modified Oswestry Questionnaire baseline, 12 weeks post intervention, 9 months post intervention
Secondary Change in Urogynecological Complaints measured using the Pelvic Floor Distress Inventory baseline, 12 weeks post intervention, 9 months post intervention
Secondary Change in Severity of Lumbopelvic and/or Abdominal Pain Visual Analog Scale baseline, 12 weeks post intervention, 9 months post intervention
Secondary Change in Perceived Function Inventory of Functional Status After Childbirth Questionnaire baseline, 12 weeks post intervention, 9 months post intervention
See also
  Status Clinical Trial Phase
Recruiting NCT04158180 - Creation and Validation of a Questionnaire Evaluating Diastasis Recti
Not yet recruiting NCT06214650 - Diastasis Recti Abdominis and a Combined Treatment With Abdominal Exercise and Radiofrequency N/A
Recruiting NCT05162612 - Anatomo-radiological Study on Semilunar Line as Risk Factor fo Diastasis Recti Abdominis
Terminated NCT04049487 - Impact of Exercise on Diastasis Rectus Abdominus N/A
Recruiting NCT06286553 - Rehabilitation of Abdominal Diastasis After Childbirth: Trunk and Inspiratory Muscle Training N/A
Completed NCT04757077 - The Association Between Pelvic Floor Muscle Function, Diastasis Recti and Postpartum Pelvic Girdle Pain - a Matched Case Control Study.