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A Study on the Efficacy of Qi-Benefiting and Fundamental-Strengthening Tuina Therapy Based on the Theory of Preventing Disease Before It Occurs in Children with Recurrent Respiratory Tract Infections (RRTIs) of the Lung-Spleen Qi Deficiency Type

A Study on the Efficacy of Qi-Benefiting and Fundamental-Strengthening Tuina Therapy Based on the Theory of Preventing Disease Before It Occurs in Children with Recurrent Respiratory Tract Infections (RRTIs) of the Lung-Spleen Qi Deficiency Type

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001344
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-06-30
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Recurrent respiratory tract infections

Interventions

Control group:Health education only
experimental group:Tuina treatment group

Sponsors

Chongqing Health Center for Women and Children
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 5 Years

Inclusion criteria

Inclusion criteria: 1: Meeting the diagnostic and pattern identification criteria 2: aged 2–5 years,regardless of gender 3: in a non-acute infection phase 4: able to cooperate with treatment and follow-up 5: completing the full course of therapy 6: the legal guardian of the child has provided informed consent and signed the informed consent form

Exclusion criteria

Exclusion criteria: 1: Children who have received treatment with other immunomodulatory agents within the past 12 months 2: children with primary immunodeficiency disorders, pulmonary hypoplasia, or swallowing dysfunction 3: children with severe concomitant primary diseases involving the heart, liver, kidneys, digestive system, or hematopoietic system 4: individuals with iatrogenic immune deficiency caused by long-term use of glucocorticoids, immunosuppressants, cytotoxic drugs, radiotherapy, or prolonged antibiotic use 5: children who are uncooperative or currently participating in other drug trials

Design outcomes

Primary

MeasureTime frame
Overall clinical response rate;

Secondary

MeasureTime frame
Serum immunoglobulin levels;Duration of each infection episode;Traditional Chinese Medicine syndrome score;Height and weight gain;Incidence of adverse events;

Countries

China

Contacts

Public ContactXuemeiLi

Chongqing Health Center for Women and Children

981342321@qq.com13508325200

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 11, 2026