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The Impact of AI-Assisted Fitness Qigong on Low Anterior Resection Syndrome, Cancer-Related Fatigue, and Quality of Life in Patients with Colorectal Cancer.

Effects of AI-assisted Health Qigong exercise on low anterior resection syndrome and quality of life in patients with colorectal cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001307
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-04-01
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

Colorectal cancer

Interventions

Qigong exercise group:Fitness Qigong Practice
AI-assisted Qigong group:ContentAI Assisted Qigong Practice
Control group:Routine Postoperative Health Education

Sponsors

Shanghai University of Sport
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) The subjects meet the diagnostic criteria for colorectal cancer as specified in the "Chinese Guidelines for the Diagnosis and Treatment of Colorectal Cancer (2023 Edition)". Patients are diagnosed with colorectal cancer based on clinical presentation, laboratory tests (occult blood in stool, colonoscopy), and imaging studies, and have undergone low anterior resection (LAR); 2) Patients with rectal cancer aged between 18 and 75 years; 3) Patients with a Karnofsky Performance Status (KPS) score greater than 80 and an Eastern Cooperative Oncology Group Performance Status (ECOG) score less than 1; 4) Patients who are conscious, able to understand and cooperate with the requirements of the study, and can accept standardized intervention protocols; 5) Patients who have signed the informed consent form and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1) Patients with a permanent stoma; 2) Patients with severe neurological diseases, cardiovascular diseases, or other major illnesses; 3) Subjects currently participating in other clinical trials; 4) Individuals who have regularly engaged in physical activities over the past 24 weeks; 5) Patients with cognitive impairments, mental disorders, or hearing/vision disabilities that prevent cooperation with interventions and assessments.

Design outcomes

Primary

MeasureTime frame
Low anterior resection syndrome;Cancer-related fatigue;Quality of life;—

Secondary

MeasureTime frame
Sleep quality;Anxiety Disorders;Depression;Six-Minute Walk;Postoperative complications;Exercise adherence;—

Countries

China

Contacts

Public ContactDong Zhu

Shanghai University of Sport

zhudong@sus.edu.cn13701937457

Outcome results

None listed

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