A comparative study on the treatment of upper crossed syndrome with three round piles and rehabilitation training

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ITMCTR

Registry ID

ITMCTR2200005710

Enrollment

Unknown

Registered

2022-03-14

Start date

2022-03-19

Completion date

Unknown

Last updated

2023-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

upper cross syndrome

Interventions

Blank control group:Blank control

Three round pile training group:Three round pile training

Rehabilitation training group:Rehabilitation training

Eligibility

Sex/Gender

All

Age

18 Years to 25 Years

Inclusion criteria

Inclusion criteria: (1) Meet the above diagnostic criteria; (2) 18 years old=age=25 years old; (3) The disease course is between 2 months and 12 months; (4) Those with bone and joint system diseases (such as congenital scoliosis, deformity, bone tuberculosis, bone tumors, etc.) are excluded; (5) Those who participated voluntarily and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) Those who are receiving other treatment; (2) Those with a history of acute trauma to the shoulder and neck or major surgery; (3) Those who do not accept the treatment plan.

Design outcomes

Primary

Measure	Time frame
Visual Analog Score;FSA;Neck, chest and shoulder soft tissue tension;FHA;	—

Secondary

Measure	Time frame
scroe of static posture of the sagittal plane;compliance assessment;HAMA;	—

Countries

China

Contacts

Public ContactMeng Letian

mengletian126@126.com19801206692

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026