Menu
Not yet recruiting NCT07632313

Health Behavior Intervention for Colorectal Cancer Patients

No phase Interventional Colorectal Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: health behavior intervention programs based on the temporal self-regulation theory are also received.
Who it may be relevant to
Registry conditions: Colorectal Cancer. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Study on Health Behavior Intervention for Colorectal Cancer Patients Based on the Theory of Time-bound Self-regulation

Overview

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.

Interventions

  • Behavioral health behavior intervention programs based on the temporal self-regulation theory are also received
    The 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

Primary outcome measures

  • health behavior [Time frame: From before the intervention (T0) to 3 months after the intervention (T2)]
Secondary outcome measures (3)
  • Health behavior intention [Time frame: From before the intervention (T0) to three months after the intervention (T2)]
  • Future Time Perspective [Time frame: From before the intervention (T0) to three months after the intervention (T2)]
  • Behavioral prepotency [Time frame: From before the intervention (T0) to three months after the intervention (T2)]

Eligibility criteria

Inclusion criteria

Age ≥ 18 years; patients who meet the diagnostic criteria for colorectal cancer outlined in the "Chinese Guidelines for the Diagnosis and Treatment of Colorectal Cancer (2023 Edition)" and for whom the time since surgery is ≥ 3 months; patients who are able to understand the study and complete the questionnaire independently; and patients who voluntarily agree to participate.

Exclusion criteria

Patients with severe cardiac, hepatic, or renal insufficiency or other serious systemic diseases; patients with cognitive or psychiatric disorders; patients with severe postoperative complications (such as anastomotic leakage or severe wound infection); patients with metastatic cancer or concurrent malignant tumors; patients with a life expectancy of less than 6 months.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Sequential
Masking
Single blind
Primary purpose
Supportive care

Study locations

China · 1 center
  • 101 Longmian Avenue, Jiangning District — Nanjing

Identifiers

NCT: NCT07632313 · 2025-SR-1017

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗