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Cross-cultural Adaptation and Validation of the Pelvic Girdle Questionnaire in French Language

Cross-cultural Adaptation and Validation of the Pelvic Girdle Questionnaire in French Language

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03436888
Acronym
PELVIC
Enrollment
134
Registered
2018-02-19
Start date
2018-03-15
Completion date
2023-08-25
Last updated
2023-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Girdle Pain, Postpartum Period, Pregnancy Related

Brief summary

The objective of this study is the adaptation of the Pelvic Girdle Questionnaire to the French language from France, and the analysis of its psychometric properties. Firstly, a translation and adaptation process will be performed according to international guidelines. Secondly, the validation process will be performed through a sample of 250 pregnant or postpartum women suffering from pelvic girdle pain. They will fill several questionnaires, including Pelvic Girdle Questionnaire, that will allow us to analyse psychometric properties of the French version.

Interventions

None listed

Sponsors

University Hospital, Caen
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Women from 18 years-old, pregnant or having given birth less than one year earlier, with PGP whose onset occurred during pregnancy or within 3 weeks after birth. Registered in the French social security system.

Exclusion criteria

* Ovarian cysts, uterine fibroids, caesarean section (if subject in postpartum period), radicular pain below the knee, previous surgery on the spine, pelvis or lower limbs, vaginismus-type pelvic pain, spondylolisthesis, inflammatory diseases, prolapse, suspected serious pathology (weakness of the lower limbs, reflex changes or loss of sensation associated with the same spinal nerve), impossibility or difficulty in understanding the questionnaires and subjects needing guardianship/supervision.

Design outcomes

Primary

MeasureTime frameDescription
Disabilityup to ten daysDisability will be measured using Pelvic Girdle Questionnaire

Secondary

MeasureTime frameDescription
Disability: Oswestry disability index1 day (First appointment)Disability will be measured using Oswestry disability index
fear-avoidance beliefs: Fear Avoidance Beliefs Questionnaire1 day (First appointment)Fear Avoidance Beliefs will be measured using Fear Avoidance Beliefs Questionnaire
Pain Catastrophizing: Pain catastrophizing scale1 day (First appointment)Pain catastrophizing will be measured using pain catastrophizing scale
health-related quality of life: SF 8 scale1 day (First appointment)Health-related quality of life will be measured using SF 8 scale
Pain: Visual Analogue Pain Rating Scale1 day (First appointment)Pain will be measured using Visual Analogue Pain Rating Scale

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026