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Clinical Trials/NCT04818411
NCT04818411
Completed
Not Applicable

Comparison of Stabilization Exercises Versus Thrust Manipulation Technique on Pelvic Girdle Pain.

Riphah International University1 site in 1 country40 target enrollmentAugust 18, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pelvic Girdle Pain
Sponsor
Riphah International University
Enrollment
40
Locations
1
Primary Endpoint
Visual analog scale
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The objective of this research is to compare the efficacy of stabilization exercise versus pelvic girdle pain thrust manipulation technique in females with postpartum pain.

Detailed Description

Pelvic-girdle pain is a mechanical disorder growing rapidly as a consequence of changing delivery pattern and changing lifestyle. Medication with synthetic drugs not only has been unable to effectively curtail the spread of this disease conditions but also is most of the times linked with co-occurring side-effects. The exercise and manual therapy-based approach could lead in reducing the functional limitations and morbidity rate in females with the postpartum pain. This research could also help in spreading the awareness globally, to Prenatal and Postnatal Hospital Caregivers.

Registry
clinicaltrials.gov
Start Date
August 18, 2019
End Date
July 26, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • • Post-partum females with the normal vaginal delivery present with pelvic girdle pain before the next conception.
  • Aged between 18 and 45
  • Posterior pelvic girdle pain located distal and/or lateral to the L5-S1
  • Pain onset during pregnancy or within 3 weeks after delivery, most recent delivery within 6 to 16 weeks
  • Positive posterior pelvic pain provocation (P4) test

Exclusion Criteria

  • Patients presenting with the history of:
  • Back pain indicating radiculopathy
  • Mechanical back pain
  • Back pain due to disc herniation
  • Rheumatological diseases
  • Neurological illness or recent surgery
  • Women who have gone through C-section

Outcomes

Primary Outcomes

Visual analog scale

Time Frame: 2 months

The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain."

Oswestry disability index

Time Frame: 2 months

The ODI score (index) is calculated as: If all 10 sections are completed the score is calculated as follows: if 16 (total scored) out of 50 (total possible score) x 100 = 32% If one section is missed (or not applicable) the score is calculated: If 16 (total scored) / 45 (total possible score) x 100 = 35.5%

Study Sites (1)

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