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Randomized Controlled Clinical Study on the Selective Spinal Manipulation Therapy for the Treatment of Children's Myopia

Randomized Controlled Clinical Study on the Selective Spinal Manipulation Therapy for the Treatment of Children's Myopia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116606
Enrollment
Unknown
Registered
2026-01-13
Start date
2025-01-13
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Myopia

Interventions

Experimental Group:Selective Spinal Tuina Manipulation Therapy
Control group:Periorbital Tuina Therapy

Sponsors

Yunnan University of Traditional Chinese Medicine/The Second Affiliated Hospital of Yunnan University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Prior to enrollment, routine ophthalmic examinations were conducted on the children, all of whom met the diagnostic criteria for simple, mild to moderate myopia; 2. The children involved in the study were aged between 6 and 12 years, with no distinction made based on gender; 3. Informed consent was obtained from both the guardians and the children; 4. Both guardians and children volunteered to participate in the clinical observation, adhered to the physician's arrangements, and cooperated with the treatment.

Exclusion criteria

Exclusion criteria: 1. Individuals with ocular inflammation, skin lesions, or infectious foci on the face; 2. Patients with severe systemic diseases, such as cardiovascular, cerebrovascular, hepatic, renal, hematological, and psychiatric disorders; 3. Individuals with a history of congenital hereditary high myopia; 4. Patients with pathological changes in the fundus of the eye due to myopia and/or significant visual impairment, as well as other ocular conditions that may affect the assessment of therapeutic outcomes; 5. Children with neurological and psychiatric disorders (such as cerebral palsy, autism, spina bifida, anorexia nervosa).

Design outcomes

Primary

MeasureTime frame
Uncorrected visual acuity;Spherical Equivalent ;

Secondary

MeasureTime frame
Axial Length;Intraocular Pressure;

Countries

China

Contacts

Public ContactXiantao Tai

Yunnan University of Traditional Chinese Medicine/The Second Affiliated Hospital of Yunnan University of Traditional Chinese Medicine

taixiantao@163.com+86 871 6595 4492

Outcome results

None listed

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