Pilates

2

Review clinical trials related to Pilates. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Core Stability, Postural Balance, and Flexibility in Healthy Women: A Comparative Study Between Pilates Practitioners and Sedentary Individuals

This study aims to compare core muscle stability, postural balance, and flexibility between healthy women who regularly practice Pilates and those with a sedentary lifestyle. The researcher will evaluate if long-term Pilates practice (5 months or more) leads to significant improvements in physical performance compared to a lack of regular exercise. Assessment tools include the Pressure Biofeedback Unit (PBU) for core activation, the McGill battery for endurance, the Y-Balance test for dynamic stability, and the Sit-and-Reach test for flexibility.

Participants needed: 55
Trial details
Age: 20-45Biological sex: FemaleType: ObservationalSponsor: Istinye UniversityUpdated: May 11, 2026Locations: 1
Eligibility criteria

Healthy female volunteers aged 20-45. [+5]

History of any surgery involving the spine, pelvis, or lower extremities within... [+7]

Status: Recruiting

Effectiveness of Pilates on Postural Correction, Core Strength and Flexibility in Younger Individuals With Non-specific Low Backache

The aim of this clinical trial is to study the effects of Pilates intervention versus conventional therapy on postural correction, core strength and flexibility in young individuals with complaint of non-specific low backache. The main question is whether the Pilates has better improvement as compared to the conventional therapy on postural correction, core strength and flexibility moreover to compare the effectiveness of two intervention. Participants of age 18-25 years and with complaint of non-specific low backache will be recruited. 50 participants will be enrolled. Participants will perform Pilates and conventional therapy for 3 times per week for six weeks. Participants will be randomly allocated to two groups and assessor blinding will be done to take baseline assessment. Assessor blinding is done to minimize biasness. Pre and Post assessments will be taken by the assessor. SPSS will be used for the analysis of the data.

Participants needed: 50
Trial details
Age: 18-25Biological sex: AllType: InterventionalSponsor: University of Health Sciences LahoreUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

Age 18-25 [+3]

prior history of trauma, fracture, spinal stenosis, severe comorbidities, spinal... [+1]