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Clinical Trials/NCT05490810
NCT05490810
Completed
Not Applicable

Effects of Trunk Stabilization Versus Activation Exercises on Pain and Disability in Postpartum Lumbo-pelvic Pain

Riphah International University1 site in 1 country30 target enrollmentFebruary 1, 2022
ConditionsPelvic Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pelvic Pain
Sponsor
Riphah International University
Enrollment
30
Locations
1
Primary Endpoint
Visual analogue scale
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

To compare the Effects of trunk stabilization versus activation exercises on pain and disability in postpartum lumbo-pelvic pain.

Detailed Description

Effects of stabilizing exercises on postpartum pelvic floor muscle function, lumbo-pelvic pain and disability. In results, stability exercises can help women with LPP enhance the function of their PFMs. Pregnancy and childbirth weakens PFMs and disrupts the load-transfer system in the lumbo-pelvic area. The use of PFMs in the right pattern can help these muscles operate better. Local stabilizing muscles are targeted during stabilization exercises, which increase pelvic motor control and stability. As per researcher knowledge there was limited evidence present on the comparison of trunk stabilization and trunk activation exercises. Therefore, this study was conducted to find the effectiveness of trunk stabilization versus activation exercises on disability and pain in postpartum women with lumbo-pelvic pain.

Registry
clinicaltrials.gov
Start Date
February 1, 2022
End Date
July 30, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 20-40
  • Female after postpartum
  • Two or more positive posterior provocation test
  • Active straight leg raises
  • Pain onset during pregnancy

Exclusion Criteria

  • Orthopedic or rheumatologic disorders
  • Intervertebral disc pathology
  • Neoplasm or previuos surgery of spine
  • History of fracture.

Outcomes

Primary Outcomes

Visual analogue scale

Time Frame: 2 weeks

Pain intensity was assessed using a visual analog scale (VAS), which is a 100-mm ungraded line with two anchors. Its left and right anchors represented the minimum and maximum intensities of pain, respectively. The participants were asked to report their current pain intensity on the VAS.

Secondary Outcomes

  • Oswestry disability index(2 weeks)

Study Sites (1)

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