Language: BG BG
← Back to results
Not yet recruiting Not applicable NCT07540195

EFFECTS OF CLINICAL PILATES ON PAIN AND QUALITY OF LIFE IN WOMEN WITH DYSPAREUNIA

No applicable phase (e.g. observational)
Conditions: Dyspareunia

Sponsor: Okan University

trial.available_in: БГ
Overview
The aim of this study is to investigate the effects of clinical Pilates exercises on pain, self-esteem, body image, depression, and quality of life in women with dyspareunia. The study addresses dyspareunia as a multifaceted health problem with psychological, social as well as physical implications. it evaluates the effects of pelvic floor-focused clinical Pilates interventions on physiological symptoms and psychosocial well-being. it also demonstrates this approach as effective, safe, and evidence-based method in the treatment of dyspareunia among women in Turkish society.
Description
A total of 20 women with dyspareunia were included in the study. The participants were divided into two groups: the Pilates group (n = 10) and the control group (n = 10). The Pilates group underwent a clinical Pilates exercise program including pelvic floor exercises, supervised by a physiotherapist, 3 days per week for 8 weeks, while no intervention was applied to the control group. Assessments were conducted before and after the program using the Visual Analog Scale (VAS), the Carol Postpartum Sexual Function and Dyspareunia Evaluation Scale (CPCFDDÖ), the Female Sexual Function Index (FSFI), the Rosenberg Self-Esteem Scale (RSES), the Body Image Scale (BIS), the Beck Depression Inventory (BDI), and the SF-36 Quality of Life Scale.
Who can participate
Inclusion Criteria: * Female participants aged 18-55 years * Sexually active * Willing to participate in the study * No communication problems * Experiencing dyspareunia Exclusion Criteria: * Having respiratory or neurological problems * Being pregnant * History of urogenital surgery
Interventions
Clinical Pilates Exercise
OTHER
Locations 1
Turkey (1)
Istanbul Okan University
Istanbul , Tuzla
Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Female only
Minimum age
18 Years
Maximum age
55 Years
Healthy volunteers
No
Start date
06.04.2026
Completion date
20.06.2026
Registry ID
NCT07540195
Source
clinicaltrials.gov
trial.inquiry_btn

Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.