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Effect of Pilates Exercises on Menopausal Symptoms

NCT06996743 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2025-05-30

No results posted yet for this study

Summary

Menopause, a significant transition in a woman's life characterized by the cessation of menstruation and a decline in ovarian function, leads to reduced levels of estrogen and progesterone. This hormonal shift is associated with a range of symptoms that can adversely affect women's quality of life, including vasomotor symptoms such as hot flashes and night sweats, psychological symptoms like mood swings and depression, as well as urogenital symptoms such as vaginal dryness and sexual dysfunction. These symptoms, collectively referred to as menopausal symptoms, can vary in severity and duration and frequently require intervention to alleviate their impact on daily life.

Conditions

  • Menopausal
  • Obese Patients
  • Pilates Exercise
  • Quality of Life and Menopause

Interventions

OTHER

reformer pilates group

Reformer Pilates exercises were applied to the pilates group twice a week for a total of 8 weeks.

OTHER

Mat pilates group

Mat Pilates exercises were applied to the pilates group twice a week for a total of 8 weeks.

OTHER

Lifestyle change group

After the doctor's check-up, routine application continued. The patient was informed about physical activity. In addition; a physical activity-based brochure prepared by the Specialist Physiotherapist was distributed to the participants in this group.

Sponsors & Collaborators

  • Batman University

    lead OTHER

Principal Investigators

  • Merve YİĞİT KOCAMER MERVE · Batman University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
45 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-09-05
Primary Completion
2024-03-15
Completion
2025-03-20

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06996743 on ClinicalTrials.gov