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Clinical efficacy study of the combined application of trinity approach and standardized family rehabilitation guidance in the treatment of postural torticollis in children

Clinical efficacy study of the combined application of trinity approach and standardized family rehabilitation guidance in the treatment of postural torticollis in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114425
Enrollment
Unknown
Registered
2025-12-11
Start date
2026-01-01
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

This study targeted children with postural CMT as the research population. Patients must meet at least four of the following criteria: ? the neutral position of the infant, tolerance to supine, prone, sitting and standing positions

Interventions

control group:Standardized family rehabilitation guidance
Experimental group:The trinity approach combined with standardized family rehabilitation guidance

Sponsors

The Third Affiliated Hospital of Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 2 Years

Inclusion criteria

Inclusion criteria: 1.The child's head is tilted to one side in the coronal plane, with the lower jaw pointing to the opposite side. This may be accompanied by facial asymmetry and restricted neck movement. 2.Physical examination may reveal asymmetry of the neck muscles. 3.The parents of the child patient signed the informed consent form. 4.The age at the initial diagnosis was <= 12 months.

Exclusion criteria

Exclusion criteria: 1.Those who do not meet the inclusion criteria for posture-related CMT; 2.Those who have received other treatments that may affect the study's outcome indicators; 3.Those who are too fearful of the treatment to cooperate at all; 4.Children with known diseases causing posture-related CMT, such as tumors, neurological disorders, strabismus, etc.

Design outcomes

Primary

MeasureTime frame
Clinical efficacy indicators ;

Secondary

MeasureTime frame
Shear wave elastography ; Parental anxiety self-assessment;

Countries

China

Contacts

Public Contactchenyuanqing

The Third Affiliated Hospital of Zhejiang Chinese Medical University

youtt_921@sina.com+86 571 8723 8203

Outcome results

None listed

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