NCT07292051

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
66

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Dec 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

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

Study Progress80%
Dec 2025Jun 2026

First Submitted

Initial submission to the registry

December 5, 2025

Completed
7 days until next milestone

Study Start

First participant enrolled

December 12, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

December 18, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2026

Last Updated

December 18, 2025

Status Verified

December 1, 2025

Enrollment Period

6 months

First QC Date

December 5, 2025

Last Update Submit

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 COMPARATOR

Group (A) will receive a core stability exercise program.

Other: Core Stability Exercise

Group (B)

EXPERIMENTAL

Group (B) will receive core stability exercise program with blood flow restriction technique.

Other: Core Stability ExerciseOther: 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.

Group (A)Group (B)

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

Group (B)

Eligibility Criteria

Age20 Years - 35 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

jilan Adel, lecturer

CONTACT

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