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NCT07200388Completed

How Emotional Granularity Helps Build Resilience in Young and Middle-Aged Colorectal Cancer Survivors

The Role of Emotional Granularity in Enhancing Resilience Among Young and Middle-Aged Colorectal Cancer Survivors: A Mixed-Methods Study

Source: ClinicalTrials.gov · Last updated 12 May 2026

Brief summary (registry, in English)

This study aims to understand how the ability to identify and describe specific emotions (called "emotional granularity") influences coping and adaptation ("resilience") in young and middle-aged colorectal cancer survivors. The main questions to be answer are: 1. How does emotional granularity help build resilience during cancer recovery? 2. How does emotion regulation contribute to resilience building? 3. What specific emotional needs and challenges do survivors experience? This is an observational study where no experimental treatments are provided. Participants will complete an online questionnaire about background, emotions, ways of managing emotions, and ability to cope with stress. A subset of participants will then be invited to take part in a private, 30-60 minute interview to share personal experiences and feelings in more detail.

Status (registry)
Completed
Study type
Observational
Enrollment
242 (actual)
First submitted
17 Sept 2025
Start date
30 Sept 2025
Primary completion date
6 May 2026
Lead sponsor
The Hong Kong Polytechnic University
NCT number
NCT07200388

What you commit to

  • Study type: Observational
  • Participants enrolled: 242
  • From 30 Sept 2025 to the primary completion date, 6 May 2026
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients who have not been informed of their cancer diagnosis due to family decision to withhold information;
  • Patients suffering from severe conditions that may affect participation or assessment, such as significant cognitive impairment, psychiatric disorders, or communication disorder.

Who the study is looking for

  • Young and middle-aged adult patients (age in the range of 18-60 years);
  • Patients diagnosed with CRC;
  • Patients have completed primary treatments (e.g., surgery, chemotherapy, and/or radiotherapy) without experiencing a recurrence of CRC;
  • Patients able to use a smartphone and agree to participate in the study.

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Second Affiliated Hospital of Soochow University
Coordinator of this site? Confirm its status
SuzhouChinaUnknown status
Kunshan First People's Hospital Affiliated to Jiangsu University
Coordinator of this site? Confirm its status
SuzhouChinaUnknown status
The First Affiliated Hospital of Soochow University
Coordinator of this site? Confirm its status
SuzhuChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.