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Effect of a Resilience Model-Based Program for Patients With Newly Diagnosed Colorectal Cancer

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National Taiwan University

Status

Completed

Conditions

Colorectal Cancer (MSI-H)

Treatments

Behavioral: Standard Care (in control arm)
Behavioral: Resilience model-based total care plan

Study type

Interventional

Funder types

Other

Identifiers

NCT03277235
201612224RIND

Details and patient eligibility

About

To develop a resilience model-based cancer prehabilitation program and evaluate its efficacy in improving resilience, alleviating symptoms, and enhancing spiritual well-being in patients with newly diagnosed colorectal cancer.

Full description

Develop and evaluate the effect of a resilience model-based total care plan on reducing fear of recurrence and GI symptom distress, resilience and improving spiritual well-being in this population.

Enrollment

128 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

The inclusion criteria were as follows: being aged ≧ 20 years, receiving a new diagnosis of stage 0-III colorectal cancer and being scheduled to undergo surgery, being aware of the diagnosis, being able to communicate in Mandarin or Taiwanese, and providing written informed consent. The exclusion criteria were as follows: receiving a diagnosis of stage IV colorectal cancer, having recurrent colorectal cancer or multiple cancers, and having a history of psychiatric disorders.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

128 participants in 2 patient groups

Resilience model-based cancer prehabilitation program plus standard care
Experimental group
Description:
12-week care plan with 5 in-person and 12 remote sessions, including both physical and psychological components.
Treatment:
Behavioral: Resilience model-based total care plan
Control
Other group
Description:
standard care
Treatment:
Behavioral: Standard Care (in control arm)

Trial contacts and locations

1

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Central trial contact

Shiow-Ching Shun, PHD

Data sourced from clinicaltrials.gov

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