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A multicenter,prospective, open, randomized, controlled study on the impact of postoperative exercise intervention on patients with colorectal cancer

A multicenter,prospective, open, randomized, controlled study on the impact of postoperative exercise intervention on patients with colorectal cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087302
Enrollment
Unknown
Registered
2024-07-24
Start date
2023-11-03
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Colorectal neoplasms

Interventions

Intervention group:On the basis of personalized exercise program, a 12-week exercise intervention strategy combining planned behavior theory and nudge theory was implemented for patients with colorect
Control group:Give the 12-week sports health education and sports guidelines recommend manual

Sponsors

Nursing Department,Shanghai Tenth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.age>18; 2.According to the American cancer society guidelines in pathology or imaging diagnostic criteria for patients diagnosed with colorectal cancer II - IV; 3.Undergoing anticancer chemotherapy and pass the safety assessment of exercise; 4.Normal function of major organs,That meet the following criteria: (1)the original ECOG physical status score of 0 ~ 1 or KPS score > 70 "dictionary" (2)HB=90g/L (14),ANC= 1.5×10^9/L,PLT=80×10^9/L,Alb=2.8g/dL,serum lipase and amylase50 ml/min; (4)EF>55%; (5)The levels of serum calcium, potassium, magnesium, within the scope of the standard 5.No hemorrhagic disease or blood coagulation dysfunction; 6.Normal state of mind and social participation ability, sense of awareness and participation ability; 7.Written informed consent signed voluntarily.

Exclusion criteria

Exclusion criteria: 1.A history of other malignant tumors 2.patients involved other drugs in clinical trials four weeks prior to the start of the study 3.patients have physical activity barriers and cannot complete required movement scheme 4.the survival time of patients <3 months

Design outcomes

Primary

MeasureTime frame
exercise adherence;

Secondary

MeasureTime frame
EORTC QLQ-C30;Cancer Fatigue Scale;6-minute walking test;Physical activity levels; Adverse event rate;

Countries

China

Contacts

Public ContactWu Qian

Shanghai Tenth People's Hospital

qian_wu2010@163.com+86 139 1621 9036

Outcome results

None listed

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