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Clinical Trials/NCT07292051
NCT07292051
Not yet recruiting
Not Applicable

Effect of Blood Flow Restriction Technique on Postpartum Pelvic Girdle Pain

Kafrelsheikh University0 sites66 target enrollmentStarted: December 12, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
66
Primary Endpoint
pelvic girdle pain intensity ( pain index )

Overview

Brief Summary

Purpose of the study :

The purpose of the current study is investigating the effect of Blood Flow Restriction Training technique on postpartum pelvic girdle pain.

Detailed Description

This study is a randomized controlled trial. To fulfill its purpose, we have two groups; control group (A) and experimental group (B) are two matched postpartum pelvic girdle pain groups. While group (A) will receive a core stability exercise program, group (B) will receive core stability exercise program with blood flow restriction technique.

The primary outcome measure will be pelvic girdle pain intensity, while the secondary outcomes will include pelvic girdle-related disability, health-related quality of life, Kinesiophobia , global improvement and ASLR-RE angle.

Treatment duration will be eight weeks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 35 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients will be eligible for the study if they met all the following criteria:
  • Are between 3 and 12 months postpartum.
  • Are aged between 20 and 35 years.
  • Have a body mass index (BMI) \< 30 kg/m².
  • Reported experiencing pelvic girdle pain-defined as pain localized between the posterior iliac crest and the gluteal fold, particularly in the vicinity of the sacroiliac joints-that either began during pregnancy or persisted after delivery .
  • Presented with a positive Active Straight Leg Raise (ASLR) test.
  • Showed positive findings in at least two of the following six pelvic pain provocation tests:
  • Posterior Pelvic Pain Provocation (P4/Thigh Thrust) Test
  • Patrick's (FABER) Test
  • Long Dorsal Sacral Ligament Test

Exclusion Criteria

  • -Patients will be excluded if they have any of the following:
  • If they were Pregnant
  • Known causes of pelvic girdle pain, such as fractures and rheumatism
  • Undergone lumbar or pelvic surgery in the past
  • Current neurological symptoms and signs in lower extremities such as lumbar radiculopathy and myelopathy
  • Cardiovascular disease
  • Experience with structured and supervised core or trunk exercise training programs

Outcomes

Primary Outcomes

pelvic girdle pain intensity ( pain index )

Time Frame: Baseline , 8 weeks and 16 weeks

In this study, pain severity will be measured using the mean of three 11-point NRS questionnaires for least, usual, and current pain over the previous 2 weeks.

Secondary Outcomes

  • pelvic girdle-related disability(Baseline , 8 weeks and 16 weeks)
  • Health-related quality of life(Baseline , 8 weeks and 16 weeks)
  • Kinesiophobia(Baseline , 8 weeks and 16 weeks)
  • Global improvement(Baseline , 8 weeks and 16 weeks)
  • Active straight leg raises repositioning error (ASLR-RE)(Baseline , 8 weeks and 16 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Nour Abdelaty Attia El-desouky

Physical Therapist

Kafrelsheikh University

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