Diastasis Recti And Weakness Of The Linea Alba Clinical Trial
Official title:
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
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 |
Verified date | September 2018 |
Source | Queen's University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
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 |
Country | Name | City | State |
---|---|---|---|
Canada | Rehabilitation Sciences Institute | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
Queen's University | University of Toronto |
Canada,
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 |
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