Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
NCT06777771

Effects of Reformer Pilates in Pregnant Women

Led by Izmir Democracy University · Updated on 2025-01-16

30

Participants Needed

1

Research Sites

81 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Pregnancy is known as a period associated with important physiological and psychological changes in women's lives. There is moderately sufficient evidence in the literature to recommend supplementing prenatal physical activity for maternal health benefits. It has been reported that physical exercise by pregnant women in the absence of obstetric contraindications will not pose a risk to the health of the mother and fetus. In the literature, there are no studies examining the effects of reformer pilates on pain, functional capacity, lumbopelvic stabilization, diastasis recti abdominis, abdominal muscle thickness, respiratory functions, pelvic floor dysfunction, urinary incontinence, sexual function, and venous insufficiency in pregnant women. Therefore, this study aimed to investigate the effects of reformer pilates on pain, functional capacity, lumbopelvic stabilization, diastasis recti abdominis, abdominal muscle thickness, respiratory functions, pelvic floor dysfunction, urinary incontinence, sexual function, and venous insufficiency in pregnant women.

CONDITIONS

Official Title

Effects of Reformer Pilates in Pregnant Women

Who Can Participate

Age: 18Years - 35Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Single pregnancy
  • Primiparous pregnancy
  • Adult pregnant women between 18 and 35 years old
  • Gestational age between 11 and 22 weeks
  • Body mass index less than 30
  • Ability to read and write
Not Eligible

You will not qualify if you...

  • Multiple pregnancies
  • History of abdominal surgery
  • Conditions contraindicating exercise such as heart disease, severe lung disease, continuous bleeding in the second or third trimester, placenta previa, risk of premature birth, rupture of membranes, preeclampsia, severe anemia
  • Not volunteering to participate
  • Missing more than 10% of training sessions

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

İzmir Democracy Univercity

Izmir, Konak, Turkey (Türkiye), 35140

Actively Recruiting

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Research Team

Ö

Özlem Çinar Özdemir, Prof.Dr.

CONTACT

K

Kübra Özonay, PhD student

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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