Clinical Trials Directory

Trials / Completed

CompletedNCT07089147

Postpartum Coccydynia and the Paris Questionnaire

The Role of the Paris Questionnaire in the Assessment of Postpartum Coccydynia: Associations With Quality of Life and Functional Outcomes

Status
Completed
Phase
Study type
Observational
Enrollment
292 (actual)
Sponsor
KTO Karatay University · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to investigate the presence of coccydynia (tailbone pain) in women who have given birth and to examine the relationship between the Paris Questionnaire and other relevant assessment tools. The relationship between the Paris questionnaire, the Low Back Outcome Score, and Quality of Life will also be evaluated.

Detailed description

Females aged between 18 and 65 years who have given birth will be included in the study. The postpartum duration of eligible participants will range from a minimum of 6 weeks to a maximum of 2 years. At the beginning of the survey, participants will be informed about the study and asked to provide their informed consent. Sociodemographic and clinical data including age, height, body weight, educational level, income status, family type, smoking status, engagement in regular physical activity, presence of chronic diseases, and obstetric history (i.e., most recent mode of delivery, number of pregnancies, number of births) will be recorded. Following this, participants will be asked to complete the Paris Questionnaire, the General Quality of Life Scale, and the Low Back Outcome Score. The relationships among the relevant questionnaires will be analyzed, and the association of the Paris Questionnaire with the other scales will be interpreted.

Conditions

Interventions

TypeNameDescription
OTHERquestionnaireParis questionnaire, EuroQool (EQ-5D-3L) Questionnaire, Low Back Outcome Score

Timeline

Start date
2025-08-01
Primary completion
2025-09-01
Completion
2025-10-01
First posted
2025-07-28
Last updated
2025-12-23

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07089147. Inclusion in this directory is not an endorsement.