Biomechanical Simulation Analysis of the Lower Extremity During Running in Males With Type A Lower Crossed Syndrome.

February 1, 2026 updated by: Shazlin Shaharudin, Universiti Sains Malaysia
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.

Study Overview

Status

Active, not recruiting

Intervention / Treatment

Detailed Description

This randomized controlled study investigates the effects of an exercise intervention on male patients with lower crossed syndrome type A. Participants who meet the eligibility criteria are randomly assigned to either an exercise intervention group or a control group. The intervention group performs a structured kettlebell-based exercise program three times per week for a duration of eight weeks, while the control group receives usual care without participation in the exercise program. Outcome measures are collected at baseline and after completion of the intervention period to evaluate changes associated with the exercise program.

Study Type

Interventional

Enrollment (Estimated)

44

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Hebei
      • Shijiazhuang, Hebei, China, 050000
        • School of Physical Education, Hebei Normal University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Exercise Intervention Group
Participants in this group perform a structured, supervised kettlebell-based exercise program three times per week for a duration of eight weeks.
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 .
Other Names:
  • Structured Kettlebell Training
No Intervention: Control Group
Participants in this group receive usual care and do not participate in the exercise intervention during the study period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pelvic Tilt Angle
Time Frame: 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.
Baseline and 8 weeks after intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 10, 2025

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2027

Study Registration Dates

First Submitted

February 1, 2026

First Submitted That Met QC Criteria

February 1, 2026

First Posted (Actual)

February 9, 2026

Study Record Updates

Last Update Posted (Actual)

February 9, 2026

Last Update Submitted That Met QC Criteria

February 1, 2026

Last Verified

December 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Lower Crossed Syndrome

Clinical Trials on Kettlebell Exercise Program

Subscribe