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Postpartum Coccydynia and the Paris Questionnaire

NCT ID: NCT07089147

Last Updated: 2025-12-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

292 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-08-01

Study Completion Date

2025-10-01

Brief Summary

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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

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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

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Postpartum Coccydynia

Keywords

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postpartum coccydynia paris questionnaire

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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females in the postpartum period

The study will include females aged between 18 and 65 years who have not previously received any treatment for coccydynia and who are within a maximum of 2 years postpartum. The study does not involve any intervention. Only a questionnaire will be administered to the females.

questionnaire

Intervention Type OTHER

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

Interventions

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questionnaire

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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Being between 18 and 65 years of age
* Having not received any previous treatment for coccydynia
* Having given birth within the last 2 years at most

Exclusion Criteria

* Those who have undergone surgical intervention on their spine
* Those with a history of malignancy
* Those with rectal or gynecological diseases
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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KTO Karatay University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Özlem Akkoyun Sert, PhD

Role: STUDY_DIRECTOR

KTO Karatay University

Locations

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Kto Karatay University

Konya, Karatay, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Peyton FW. Coccygodynia in women. Indiana Med. 1988 Aug;81(8):697-8. No abstract available.

Reference Type RESULT
PMID: 3171154 (View on PubMed)

Maigne JY, Rusakiewicz F, Diouf M. Postpartum coccydynia: a case series study of 57 women. Eur J Phys Rehabil Med. 2012 Sep;48(3):387-92. Epub 2012 Jul 23.

Reference Type RESULT
PMID: 22820826 (View on PubMed)

Other Identifiers

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2024/044

Identifier Type: -

Identifier Source: org_study_id