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The Use of WeChat Mini Program During Induced Remission in the Management of Early Crohn's Disease Patients: a Non-Inferiority Trial

The Use of WeChat Mini Program During Induced Remission in the Management of Early Crohn's Disease Patients: a Non-Inferiority Trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043539
Enrollment
Unknown
Registered
2021-02-21
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-06-14

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

Conditions

inflammatory bowel disease

Interventions

Offline follow-up group:Standard outpatient follow-up
Wechat mini program group:Online follow-up

Sponsors

The Affiliated Wuxi People's Hospital, Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. First diagnosed as Crohn's disease; 2. under the mild to moderate activity period; 3. Aged >= 18 and <= 75 years; 4. according to the clinician's judgment, azathioprine is proposed to be used as the treatment of induced remission; 5. with the educational level of primary school or above, who can understand the content of this study; 6. voluntarily participate in the study, and can receive the randomization, as well as sign informed consent; 7. have smartphone and network and be able to participate in online follow-up.

Exclusion criteria

Exclusion criteria: 1. Severe IBD patients requiring close monitoring; 2. with previous usage of corticosteroids, immunomodulators and biological agents; 3. with possible/planned surgical intervention in three to six months; 4. with short bowel syndrome, experienced more than two bowel operations, fistula surgery, bag storage surgery or large-scale bowel surgery; 5. with abdominal abscess infection, fistula, tumor history; 6. combined with severe primary disease including cardiovascular and cerebrovascular, liver, kidney, etc; 7. women who are pregnant; 8. those who are not suitable for inclusion judged by researchers.

Design outcomes

Primary

MeasureTime frame
Crohn's disease activity index, CDAI;HRQOL;rate of clinical remission;

Secondary

MeasureTime frame
C-reactive proteins;blood routine examination;blood biochemical indexes;reporting rate of adverse drug reactions;Incidence of severe adverse drug reactions;Compliance;usability;cost;

Countries

China

Contacts

Public ContactSunJing

The Affiliated Wuxi People's Hospital, Nanjing Medical University

jingdianjing@126.com+86 13675151962

Outcome results

None listed

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