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Research on the Application of an AI Short Video-Based Mobile Health Intervention System in the Perioperative Management of Patients with Mixed Hemorrhoids

Research on the Application of an AI Short Video-Based Mobile Health Intervention System in the Perioperative Management of Patients with Mixed Hemorrhoids

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126273
Enrollment
Unknown
Registered
2026-06-05
Start date
2026-06-08
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Combined hemorrhoids

Interventions

Intervention Group:Routine diagnosis and treatment + AI short video-based mobile health intervention system
Control Group:Routine diagnosis and treatment combined with traditional health education

Sponsors

The Third People's Hospital of Chengdu
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18–60 years; 2.Treated at the Department of Anorectal Surgery of our hospital, with a definite diagnosis of mixed hemorrhoids and planned elective surgical treatment; 3.Requiring perioperative health management (including preoperative preparation and postoperative rehabilitation); 4.Capable of using a smartphone, able to read text, watch videos, and perform basic operations; 5.Have followed the designated health education WeChat public account for the study, and be able to participate in video viewing, daily check-ins, and related interactions; 6.Volunteer to participate in this study and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1.Presence of severe cognitive impairment, mental illness, or communication disorders that prevent understanding of the study content or cooperation with follow-up; 2.Inability to use a smartphone independently or lack of stable internet access; 3.Presence of severe underlying diseases (e.g., severe cardiac, hepatic, or renal insufficiency) or critical illness that makes the patient unsuitable for participation in this study; 4.Undergoing special surgical procedures or having complex anorectal diseases requiring concurrent treatment (e.g., anal fistula, anal fissure) that may affect postoperative recovery assessment; 5.Concurrent participation in other interventional clinical studies that may affect the results of this study; 6.Other conditions deemed by the investigator as making the patient unsuitable for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
Quality of Life;Pain level;Wound healing status;Anxiety and depression levels;Intervention satisfaction;Self-efficacy;eHealth literacy;

Secondary

MeasureTime frame
Process outcome indicators;

Countries

China

Contacts

Public ContactLiu Li

The Third People's Hospital of Chengdu

cdsyyywbll@163.com+86 28 6131 8455

Outcome results

None listed

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