Status:

NOT_YET_RECRUITING

Adapted Physical Activity and Pelvic Floor Function for Pelvic Girdle Pain During Pregnancy

Lead Sponsor:

Haute Ecole de Santé Vaud

Collaborating Sponsors:

La Tour Hospital

Conditions:

Pelvic Girdle Pain

Pregnancy

Eligibility:

FEMALE

18+ years

Phase:

NA

Brief Summary

Pelvic girdle pain (PGP) is a common condition during pregnancy, affecting up to two-thirds of women. It can cause significant discomfort, limit daily activities, and reduce quality of life. Current t...

Detailed Description

Background and Rationale Pregnancy induces substantial morphological, hormonal, and biomechanical changes that increase the risk of musculoskeletal pain, particularly pelvic girdle pain (PGP). Up to ...

Eligibility Criteria

Inclusion

  • Pregnant women aged ≥18 years
  • Gestational age ≤27 weeks at enrollment
  • Clinically confirmed pelvic girdle pain, defined as:
  • Pain localized between the posterior iliac crest and the gluteal fold, particularly around the sacroiliac joints and/or pubic symphysis, Pain intensity ≥3/10 on Visual Analog Scale (VAS), At least 3 positive clinical tests among: Posterior Pelvic Pain Provocation (P4) test, Patrick's FABER, Menell's test, Active Straight Leg Raise (ASLR), and palpation of long dorsal sacroiliac ligament or symphysis pubis
  • Ability to understand and provide written informed consent

Exclusion

  • Isolated low back pain without pelvic involvement
  • Contraindications to exercise during pregnancy (e.g., severe preeclampsia, placenta previa after 26 weeks, risk of preterm labor, ruptured membranes, significant cardiac or pulmonary disease)
  • Neurological, rheumatologic, or orthopedic conditions that may interfere with participation
  • Insufficient French language proficiency to understand questionnaires and instructions
  • Participation in another interventional study that could affect outcomes

Key Trial Info

Start Date :

September 30 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 31 2027

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT07186504

Start Date

September 30 2025

End Date

October 31 2027

Last Update

September 22 2025

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