NCT07632313

Brief Summary

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.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at below P25 for not_applicable colorectal-cancer

Timeline
8mo left

Started Jun 2026

Shorter than P25 for not_applicable colorectal-cancer

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 2, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 8, 2026

Completed
7 days until next milestone

Study Start

First participant enrolled

June 15, 2026

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2027

Last Updated

June 8, 2026

Status Verified

June 1, 2026

Enrollment Period

7 months

First QC Date

June 2, 2026

Last Update Submit

June 2, 2026

Conditions

Colorectal Cancer

Keywords

health behaviorTemporal Self-Regulation Theory

Outcome Measures

Primary Outcomes (1)

  • health behavior

    Measured through the Health Behavior Scale for Cancer Patient

    From before the intervention (T0) to 3 months after the intervention (T2)

Secondary Outcomes (3)

  • Health behavior intention

    From before the intervention (T0) to three months after the intervention (T2)

  • Future Time Perspective

    From before the intervention (T0) to three months after the intervention (T2)

  • Behavioral prepotency

    From before the intervention (T0) to three months after the intervention (T2)

Study Arms (2)

intervention group

EXPERIMENTAL

Based on providing routine post-operative health education services for colorectal cancer patients in the hospital, additional health behavior intervention programs based on the theory of time-limited self-regulation are also received.

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

control group

NO INTERVENTION

Regular post-operative health education services for colorectal cancer

Interventions

health behavior intervention programs based on the temporal self-regulation theory are also receivedBEHAVIORAL

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 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

intervention group

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

101 Longmian Avenue, Jiangning District

Nanjing, Jiangsu, China

Location

MeSH Terms

Conditions

Colorectal NeoplasmsHealth Behavior

Condition Hierarchy (Ancestors)

Intestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal DiseasesRectal DiseasesBehavior

Central Study Contacts

Xiao X Hu

CONTACT

+86 187521129181937505957@qq.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
SEQUENTIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Xiaoxiao Hu

Study Record Dates

First Submitted

June 2, 2026

First Posted

June 8, 2026

Study Start

June 15, 2026

Primary Completion (Estimated)

December 30, 2026

Study Completion (Estimated)

January 30, 2027

Last Updated

June 8, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

IPD sharing is not allowed due to ethical and consent-related restrictions.

Locations

CN(1)