- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07397143
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
Conditions
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:
- Adult males aged 18-25 years
- Anterior pelvic tilt angle greater than 15°
- Positive bilateral Thomas test
- Observed mild hip flexion and knee flexion during standing posture
- No history of spinal, pelvic, or lower limb surgeries
Exclusion Criteria:
- Congenital anomalies of the lumbar vertebrae
- 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:
|
|
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.
Sponsor
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
Keywords
Other Study ID Numbers
- USM/JEPeM/KK/24090808
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
-
Riphah International UniversityCompleted
-
Foundation University IslamabadCompleted
-
Riphah International UniversityNot yet recruitingUpper Crossed SyndromePakistan
-
Riphah International UniversityNot yet recruitingUpper Crossed SyndromePakistan
-
Riphah International UniversityRecruitingUpper Crossed SyndromePakistan
-
Riphah International UniversityCompletedUpper Crossed SyndromePakistan
-
Universiti Putra MalaysiaCompletedUpper Crossed SyndormeChina
-
Cairo UniversityNot yet recruitingUpper Crossed Syndrome
-
China Medical University HospitalRecruiting
-
Riphah International UniversityRecruitingChildren, Only | Upper Crossed SyndromePakistan
Clinical Trials on Kettlebell Exercise Program
-
Hacettepe UniversityRecruitingRotator Cuff Injuries | Shoulder PainTurkey (Türkiye)
-
University of ThessalyCompleted
-
Saglik Bilimleri UniversitesiIstanbul University - Cerrahpasa (IUC)CompletedPulmonary Arterial HypertensionTurkey
-
University Hospital, Basel, SwitzerlandCompletedChild Development | Feasibility Studies | Primary Health Care | Muscle Strength | Resistance Training | Schools | Preventive Health Services | Schools / Organization & AdministrationSwitzerland
-
Karabuk UniversityCompletedExercise Performance | Physical Fitness | Neuromuscular FunctionTurkey (Türkiye)
-
University of Central FloridaCompleted
-
University of Central FloridaCompletedMuscle Weakness | Muscle Soreness | Muscle TendernessUnited States
-
University of Central FloridaCompleted
-
Keller Army Community HospitalTerminatedAthletic Performance | Weight LiftingUnited States
-
Azienda Sanitaria Locale CN1 CuneoRecruiting