The Effect of Conservative Interventions on the Signs and Symptoms of Diastasis Recti
NCT ID: NCT02268110
Last Updated: 2018-09-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
32 participants
INTERVENTIONAL
2014-08-31
2018-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Supervised exercise therapy
Participants will receive 12 sessions with a physiotherapist where they will receive instructions on body mechanics, and be given a progressive abdominal exercise program
Exercise therapy
Supervised exercise therapy with a 12 week progressive abdominal exercise home program for
Abdominal binding
Participants will be fitted for an abdominal binder and asked to wear it for a period of 12 weeks.
Abdominal binding
Wearing an abdominal binder for 12 weeks
Exercise therapy and Abdominal Binding
Participants will attend 12 sessions with a physiotherapist, and receive an abdominal binder
Exercise therapy
Supervised exercise therapy with a 12 week progressive abdominal exercise home program for
Abdominal binding
Wearing an abdominal binder for 12 weeks
Control
Participants will not receive an intervention during the study period
No interventions assigned to this group
Interventions
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Exercise therapy
Supervised exercise therapy with a 12 week progressive abdominal exercise home program for
Abdominal binding
Wearing an abdominal binder for 12 weeks
Eligibility Criteria
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Inclusion Criteria
* 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
* diagnosed with neurological impairments affecting the central nervous system or sacral nerves
* diagnosed with connective tissue disorders
18 Years
35 Years
FEMALE
No
Sponsors
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University of Toronto
OTHER
Queen's University
OTHER
Responsible Party
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Nadia Keshwani
PhD candidate
Principal Investigators
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McLean Linda, PhD
Role: STUDY_DIRECTOR
Queen's University
Locations
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Rehabilitation Sciences Institute
Toronto, Ontario, Canada
Countries
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Other Identifiers
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REH-566-13
Identifier Type: -
Identifier Source: org_study_id
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