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Search / Trial NCT02648607

Management of Chronic Post-Partum Pelvic Girdle Pain Study

Launched by UNIVERSITY OF PLYMOUTH · Jan 6, 2016

Trial Information

Current as of June 26, 2025

Completed

Keywords

Pelvic Girdle Pain Chronic Pelvic Girdle Pain Symphysis Pubis Dysfunction Sacroiliac Joint Dysfunction Physiotherapy Physical Therapy Orthoses Orthosis Orthotic Devices

ClinConnect Summary

Pelvic girdle pain (PGP) occurs in 70% of pregnant women; of whom 25% have severe pain and 8% severe disability requiring the use of crutches, wheelchair or confinement to bed (Wu et al, 2004). At a personal level, women with PGP find that everyday activities such as turning in bed, prolonged walking, or carrying items may cause pain; impacting negatively on quality of life (Wang et al, 2004). In economic terms societal costs are significant, mainly as a consequence of work absenteeism; with 20% of people requiring an average of 7 weeks sick leave (Noren et al, 1997). The impact of this pro...

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria: Women with PGP (commenced or aggravated during pregnancy) will be included if they:
  • have symptoms that continued for \> 3 months following birth,
  • have PGP that causes walking and/or stair climbing to be bothersome (as determined by a score of at least 2 on a 10 point visual analogue scale)
  • are positive on at least 3 out of 7 pain provocation tests (see screening section below)
  • Exclusion Criteria: Women will be excluded if they have:
  • A recent history/signs or symptoms indicative of serious causes of pain that might be inflammatory infective, traumatic, neoplastic, degenerative or metabolic.
  • In particular exclusion will occur if following questioning or clinical examination there is evidence of:
  • trauma
  • Indicators of serious pathology
  • steroid use
  • drug abuse
  • HIV infection
  • immunosuppressed state
  • neurological symptoms/signs (including cauda-equina)
  • fever
  • systemically unwell
  • obstetric complications
  • pain that does not improve with rest/severe disabling pain
  • history of chronic back or pelvic pain requiring surgery.
  • a known skin allergy to Lycra

About University Of Plymouth

The University of Plymouth is a renowned academic institution dedicated to advancing research and innovation in various fields, including health and clinical sciences. As a clinical trial sponsor, the university leverages its multidisciplinary expertise and state-of-the-art facilities to conduct rigorous research aimed at improving patient outcomes and informing healthcare practices. With a commitment to ethical standards and collaboration, the University of Plymouth fosters partnerships with healthcare providers, industry stakeholders, and regulatory bodies to ensure the successful design, implementation, and dissemination of clinical trials that contribute to the body of medical knowledge.

Locations

Bristol, Avon, United Kingdom

Plymouth, Devon, United Kingdom

Patients applied

0 patients applied

Trial Officials

Lee Cameron

Principal Investigator

University of Plymouth

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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