Prenatal Pilates and Postpartum Ligamentous Laxity

NCT ID: NCT07344857

Last Updated: 2026-01-22

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

42 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-11-20

Study Completion Date

2026-01-15

Brief Summary

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Pregnancy induces hormonal and biomechanical adaptations that increase ligamentous laxity, which may persist into the postpartum period and contribute to joint instability, pain, and functional limitations. Although prenatal Pilates has been shown to prevent the progression of ligamentous laxity during pregnancy, its effects on postpartum musculoskeletal recovery remain unclear. This longitudinal follow-up of a randomized controlled trial evaluated ligamentous recovery at 6 weeks postpartum in women who participated in a structured prenatal Pilates program continued until childbirth, compared with women receiving standard prenatal care. Postpartum ligamentous laxity, generalized joint hypermobility, and activity limitations related to pelvic girdle pain were assessed using objective and clinical measures. The study aimed to determine whether prenatal Pilates facilitates early postpartum ligamentous recovery and supports functional outcomes during the early postpartum period.

Detailed Description

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Conditions

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Laxity of Ligament Pregnancy Pilates Exercise

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Pilates Group

Participants in the Pilates group attended supervised 60-minute sessions twice weekly for eight weeks, led by a certified physiotherapist trained by the Australian Institute of Pilates and Physiotherapy.

No interventions assigned to this group

Control Group

The control group received standard prenatal care and ergonomic advice, and did not participate in any exercise training.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Aged between 18-35 years
* In the 6th week of post-partum
* Voluntary participation in the study

Exclusion Criteria

* Cardiovascular or pulmonary diseases
* Prior participation in structured physical activity programs
Minimum Eligible Age

20 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Ankara Medipol University

OTHER

Sponsor Role lead

Responsible Party

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Selcan Suicmez

Research Asst.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Ankara Medipol University

Ankara, Altındağ, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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AnkaraMedipolU-FTR-2025-223

Identifier Type: -

Identifier Source: org_study_id

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