NCT07397143

Brief 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.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
20mo left

Started Oct 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress26%
Oct 2025Dec 2027

Study Start

First participant enrolled

October 10, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

February 1, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

February 9, 2026

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2027

Last Updated

February 9, 2026

Status Verified

December 1, 2025

Enrollment Period

1.2 years

First QC Date

February 1, 2026

Last Update Submit

February 1, 2026

Conditions

Keywords

Lower Crossed SyndromeExercise InterventionKettlebell TrainingPostural ImbalanceMuscle Imbalance

Outcome Measures

Primary Outcomes (1)

  • Pelvic Tilt Angle

    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

Study Arms (2)

Exercise Intervention Group

EXPERIMENTAL

Participants in this group perform a structured, supervised kettlebell-based exercise program three times per week for a duration of eight weeks.

Other: Kettlebell Exercise Program

Control Group

NO INTERVENTION

Participants in this group receive usual care and do not participate in the exercise intervention during the study period.

Interventions

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 .

Also known as: Structured Kettlebell Training
Exercise Intervention Group

Eligibility Criteria

Age18 Years - 25 Years
Sexmale
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • Congenital anomalies of the lumbar vertebrae
  • Severe cardiovascular, neurological, or vascular diseases

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

School of Physical Education, Hebei Normal University

Shijiazhuang, Hebei, 050000, China

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

February 1, 2026

First Posted

February 9, 2026

Study Start

October 10, 2025

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2027

Last Updated

February 9, 2026

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared.

Locations