Application of parent-child dyadic orofacial myofunctional therapy in children post-Adenoidectomy

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400091466

Enrollment

Unknown

Registered

2024-10-29

Start date

2024-10-31

Completion date

Unknown

Last updated

2024-11-04

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

Conditions

adenoid hypertrophy

Interventions

Intervention Group:parent-child dyadic orofacial myofunctional therapy

Control group:Regular nursing intervention and discharge follow-up

Eligibility

Sex/Gender

All

Age

3 Years to 7 Years

Inclusion criteria

Inclusion criteria: 1) Children with potential facial changes undergoing AT for the first time. 2) Children and main caregivers with good communication abilities in Chinese/English. 3) Children aged 3-7 years and main caregivers aged 18-45 years. 4) Voluntary participation and informed consent.

Exclusion criteria

Exclusion criteria: 1) Severe mental illness or cognitive impairment. 2) Children with congenital craniofacial deformity. 3) Main caregivers are not their parents. 4) Inability to access the internet daily. 5) Long-term outing plans (>1 month). 6) Participation in other studies.

Design outcomes

Primary

Measure	Time frame
orofacial myofunction;parental care abilities;	—

Secondary

Measure	Time frame
engagement from PRO;parental reflection functioning;	—

Countries

China

Contacts

Public ContactHaowei Du/ Aimin Wang

Qingdao University/ the Affiliated Hospital of Qingdao University

mdr613@163.com+86 136 5869 7921

Outcome results

None listed

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