Skip to content

Study on the construction and application of teach-back based health education program for patients with Endoscopic submncosal disection

Study on the construction and application of teach-back based health education program for patients with Endoscopic submncosal disection

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125333
Enrollment
Unknown
Registered
2026-05-25
Start date
2026-05-25
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

None listed

Interventions

Control group:Routine health education related to endoscopic submucosal dissection (ESD)
Intervention group:In addition to receiving routine health education related to endoscopic submucosal dissection (ESD), the subjects in the intervention group were given digital education programs bas

Sponsors

The First Affliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Preoperative pathological examination confirms well/moderately differentiated differentiated adenocarcinoma or intramucosal carcinoma, meeting the surgical indications for ESD, and patients voluntarily receive ESD treatment. 2.Aged >=18 years old, clear consciousness, normal verbal expression ability, and able to communicate in Mandarin. 3.Provide informed consent and are willing to participate in this study. 4.Reside in the local city or surrounding counties and cities.

Exclusion criteria

Exclusion criteria: 1.Patients with consciousness disturbance or diseases impairing comprehension ability. 2.Those with cancer metastasis and ineligible for ESD surgery. 3.Patients complicated with severe insufficiency of heart, liver, brain or kidney function. 4.Patients with severe mental disorders. 5.Those with severe physical dysfunction and inability to take care of themselves in daily life. 6.Participants concurrently enrolled in other interventional clinical studies.

Design outcomes

Primary

MeasureTime frame
Mishel Uncertainty in lIness Scale for Patients Undergoing ESD;

Secondary

MeasureTime frame
Patient Satisfaction Questionnaire;

Countries

China

Contacts

Public ContactXuduo

The First Affliated Hospital of Wenzhou MedicalUniversity

12148117@qq.com+86 55579552

Outcome results

None listed

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