Skip to main content
OpenTrials
Completed

NCT Number: NCT03436888

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Pelvic Girdle Pain Musculoskeletal Pain Neurologic Manifestations Pain Pathological Conditions, Signs and Symptoms Pelvic Pain Postpartum Period Pregnancy Related Signs and Symptoms

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Caen University Hospital, Caen, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. Disability

    Time frame: up to ten days

    Disability will be measured using Pelvic Girdle Questionnaire

Secondary outcomes

  1. Disability: Oswestry disability index

    Time frame: 1 day (First appointment)

    Disability will be measured using Oswestry disability index

  2. fear-avoidance beliefs: Fear Avoidance Beliefs Questionnaire

    Time frame: 1 day (First appointment)

    Fear Avoidance Beliefs will be measured using Fear Avoidance Beliefs Questionnaire

  3. Pain Catastrophizing: Pain catastrophizing scale

    Time frame: 1 day (First appointment)

    Pain catastrophizing will be measured using pain catastrophizing scale

  4. health-related quality of life: SF 8 scale

    Time frame: 1 day (First appointment)

    Health-related quality of life will be measured using SF 8 scale

  5. Pain: Visual Analogue Pain Rating Scale

    Time frame: 1 day (First appointment)

    Pain will be measured using Visual Analogue Pain Rating Scale

Sponsors and collaborators

Lead sponsor

University Hospital, Caen

Other

Registry information

Acronym: PELVIC

Important dates

Study start
2018
Primary completion
2023
Study completion
2023
First posted
Feb 19, 2018
Registry last updated
Nov 28, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.