Kettlebell Exercise Program: A structured, supervised kettlebell-based exercise program performed three times per week for eight weeks. Each session lasts approximately 40 minutes and includes warm-up, kettlebell exercises targeting core and lower limb muscles, and cool-down. The program is designed to improve muscle balance and postural control in male patients with Type A Lower Crossed Syndrome .
Study summary
This study aims to examine the effects of an 8-week exercise program on male patients with lower crossed syndrome type A. Participants are randomly assigned to either an exercise group or a control group. The exercise group takes part in a supervised kettlebell-based exercise program three times per week for eight weeks, while the control group receives usual care without the exercise program. Measurements are taken before and after the intervention to compare changes between the two groups.
Eligibility
Sex
MALE
Min age
18 Years
Max age
25 Years
Healthy volunteers
No
Inclusion Criteria:
1. Adult males aged 18-25 years
2. Anterior pelvic tilt angle greater than 15°
3. Positive bilateral Thomas test
4. Observed mild hip flexion and knee flexion during standing posture
5. No history of spinal, pelvic, or lower limb surgeries
Exclusion Criteria:
1. Congenital anomalies of the lumbar vertebrae
2. Severe cardiovascular, neurological, or vascular diseases
Primary outcome measure(s)
Pelvic Tilt Angle — Baseline and 8 weeks after intervention Changes in pelvic tilt angle will be measured using the angle of the line connecting the Anterior Superior Iliac Spine (ASIS) and the Posterior Superior Iliac Spine (PSIS) relative to the horizontal, comparing pre- and post-intervention values between the exercise intervention group and the control group. The primary objective is to evaluate whether the kettlebell exercise program reduces the anterior pelvic tilt angle in male patients with Type A Lower Crossed Syndrome.
Trial sites (1)
Facility
City
Region
Status
School of Physical Education, Hebei Normal University
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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