About this trial
Develop a health behavior intervention plan based on patients' needs and preferences, and preliminarily apply and evaluate the feasibility and effectiveness of this intervention plan for patients with colorectal cancer.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial design
Sequential
Treatments tested in this trial
health behavior intervention programs based on the temporal self-regulation theory are also received
BehavioralThe intervention group received additional health behavior intervention programs based on the temporal self-regulation theory in addition to the routine post-operative health education services provided by the hospital. The intervention period was set as 1 session per week for a total of 6 weeks, each session lasting approximately 45-60 minutes. The intervention was conducted in a combination of offline and online guidance and support. Before the intervention, baseline assessments were conducted for the research subjects, and intervention manuals, demonstration videos, and other tools were distributed. From the 1st to the 5th week, corresponding module measures were implemented according to the intervention framework, including looking to the future, intention strengthening, habit shaping, and self-control. In the 6th week, progress summaries, feedback, and long-term plan formulation were carried out. Throughout the process, online WeChat/QQ support groups/Tencent Meeting were u
Treatment groups
Trial outcomes
Primary outcomes
health behavior
Measured through the Health Behavior Scale for Cancer Patient
Secondary outcomes
Health behavior intention
Measured through the Health Behavior Intention Scale
Future Time Perspective
Measured through the Consideration of Future Consequences Scale
Behavioral prepotency
Measured through the Self-Reported Behavioral Automaticity Index
Sponsors and contacts
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