- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06168643
Effects of Core Stability Exercise With Pregnancy Support Belt in Pubic Symphysis Dysfunction.
Effects of Core Stability Exercises With And Without Pregnancy Support Belt On Pain, Function And Disability In Symphysis Pubis Dysfunction During Pregnancy.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Imran Amjad, Post Doc
- Phone Number: 03324390125
- Email: imran.amjad@riphah.edu.pk
Study Locations
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Punjab
-
Lahore, Punjab, Pakistan
- Recruiting
- Riphah International University, Lahore
-
Contact:
- Adeela Arif, Mphil
- Phone Number: 03320845723
- Email: adeela.arif@riphah.edu.pk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Age 25-35 years females Have pain in the region of pubic symphysis, with or without radiation to the groin.
Have pain during stair climbing, turning over in bed, standing on one leg. Have tenderness on palpation of symphysis pubis. Have positive active straight leg raise (ASLR) test result
Exclusion Criteria:
Medical conditions preventing use of pregnancy support belts. Pregnant females having SPD but with absolute contraindications to exercise. Posterior (lumber spine or sacroiliac joint) pain that was considered worse than the symphysis pubis pain
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Core stability
|
Physical therapy interventions will include core stability exercises which will be demonstrated and will be checked if they are being performed correctly.
The exercises guided shall be performed 3 times daily and logbook will be provided to keep the record of exercise program.
|
|
Experimental: Core stability with pregnancy support belt
|
Participants will receive same information and exercises as those in Group A. they will also receive pregnancy support belt.
The logbook will be provided to keep the record of hours the belt has been worn along with exercise record.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Roland-Morris Questionnaire (modified)
Time Frame: 6th week
|
Roland-Morris Disability Questionnaire (RMDQ) is designed to assess self-rated physical disability caused by low back pain.
This scale is used on subjects of age more than 12 years.
Each question is worth one point so score can range from 0 (no disability) to 24 (severe disability).
|
6th week
|
|
Numerical pain rating scale
Time Frame: 6th week
|
The Numerical pain rating scale is the most commonly used pain scale in the health care.
This scale is used on subjects of age more than 9.
By using this scale ask the participant to rate their pain orally by giving the numbers from 0-10
|
6th week
|
|
Pain Specific Functional Scale
Time Frame: 6th Week
|
The PSFS is a self-reported valid, reliable, and responsive outcome measure for patients with musculoskeletal problems.
Patients are asked to identify up to five important activities they are unable to perform and rate (on an 11-point scale) the current level of difficulty associated with each activity."0"
represents "unable to perform" and "10" represents "able to perform at prior level
|
6th Week
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Depledge J, McNair PJ, Keal-Smith C, Williams M. Management of symphysis pubis dysfunction during pregnancy using exercise and pelvic support belts. Phys Ther. 2005 Dec;85(12):1290-300.
- Jain S, Eedarapalli P, Jamjute P, Sawdy R. Symphysis pubis dysfunction: a practical approach to management. The Obstetrician & Gynaecologist. 2006;8(3):153-8.
- Maclennan AH, Maclennan SC. Symptom-giving pelvic girdle relaxation of pregnancy, postnatal pelvic joint syndrome and developmental dysplasia of the hip. Acta Obstetricia et Gynecologica Scandinavica. 1997;76(8):760-4.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Ayesha Sarwar
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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-
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