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NCT Number: NCT07292051

Effect of Blood Flow Restriction Technique on Postpartum Pelvic Girdle Pain

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.

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Key information

Age range

20 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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
  • Pelvic Compression Test
  • Pelvic Distraction (Separation) Test
  • Sacral Thrust 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
  • Cancer
  • Cardiovascular disease
  • Experience with structured and supervised core or trunk exercise training programs

Treatment and study plan

Core stability exercise

Other

Patients will receive specific core stabilizing exercises, focusing on Pelvic floor muscles ,Gluteus maximus, Gluteus Medius, specific abdominal muscles , the lumbar multifidus, and Erector spinae.

Blood Flow Restriction Technique

Other

Patients will receive the same core stability exercise added to Blood Flow Restriction Technique

Primary outcomes

  1. 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

  1. pelvic girdle-related disability

    Time frame: Baseline , 8 weeks and 16 weeks

    pelvic girdle-related disability, measured by pelvic girdle questionnaire (PGQ)

  2. Health-related quality of life

    Time frame: Baseline , 8 weeks and 16 weeks

    Health-related quality of life, measured by the Arabic version of European quality of life-Five-Dimension Five-Level Instrument (EQ-5d-5L)

  3. Kinesiophobia

    Time frame: Baseline , 8 weeks and 16 weeks

    Kinesiophobia measured by an Arabic Tampa scale

  4. Global improvement

    Time frame: Baseline , 8 weeks and 16 weeks

    Global improvement measured by global rating of change (GROC) scale

  5. Active straight leg raises repositioning error (ASLR-RE)

    Time frame: Baseline , 8 weeks and 16 weeks

    ASLR-RE angle, measured by Image J

Study contacts

Contact information is provided by the study sponsor or research team.

jilan Adel, lecturer

CONTACT

[email protected]

01007519909 ext. +20

Sponsors and collaborators

Lead sponsor

Kafrelsheikh University

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Dec 18, 2025
Registry last updated
Dec 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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