Effect of Blood Flow Restriction Technique on Postpartum Pelvic Girdle Pain
1 other identifier
interventional
66
0 countries
N/A
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2025
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 5, 2025
CompletedStudy Start
First participant enrolled
December 12, 2025
CompletedFirst Posted
Study publicly available on registry
December 18, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 15, 2026
December 18, 2025
December 1, 2025
6 months
December 5, 2025
December 5, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
pelvic girdle pain intensity ( pain index )
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.
Baseline , 8 weeks and 16 weeks
Secondary Outcomes (5)
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
Study Arms (2)
Group (A)
ACTIVE COMPARATORGroup (A) will receive a core stability exercise program.
Group (B)
EXPERIMENTALGroup (B) will receive core stability exercise program with blood flow restriction technique.
Interventions
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.
Patients will receive the same core stability exercise added to Blood Flow Restriction Technique
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Physical Therapist
Study Record Dates
First Submitted
December 5, 2025
First Posted
December 18, 2025
Study Start
December 12, 2025
Primary Completion (Estimated)
June 15, 2026
Study Completion (Estimated)
June 15, 2026
Last Updated
December 18, 2025
Record last verified: 2025-12