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NCT07158671Not yet recruiting

The Effectiveness of the mHealth Survivorship Program on Enhancing Health-related Quality of Life Among Colorectal Cancer Survivors

The Effectiveness of the mHealth Survivorship Program on Enhancing Health-related Quality of Life Among Colorectal Cancer Survivors: Randomised Controlled Trial

Source: ClinicalTrials.gov · Last updated 8 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this clinical trial is to evaluate the effectiveness of the mHealth survivorship program in enhancing health-related quality of life among colorectal cancer survivors. It is hypothesized that participants receiving the mHealth-based survivorship program will report significantly higher levels of health-related quality of life and a lower level of distress, depression, anxiety, fatigue, and bowel dysfunction compared to those in the control group. Participants in the intervention group will: Use the survivorship programme through mHealth every day for 3 months Be called by the healthcare provider every 2 weeks for consultation Participants in the control group will receive the usual care

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
210 (estimated)
First submitted
19 Aug 2025
Start date
1 Sept 2025
Primary completion date
30 Jun 2027
Lead sponsor
The Nethersole School of Nursing
NCT number
NCT07158671

What you commit to

  • Study type: Interventional
  • Planned participants: 210
  • From 1 Sept 2025 to the primary completion date, 30 Jun 2027
  • No sites listed in no 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.

Prior treatment

  • receiving anxiety or depression treatment or cognitive/learning problems.

Other illness

  • mental health diseases;

Who the study is looking for

  • be 18 or older (1);
  • Vietnamese-speaking CRC patients who have completed active treatment and are preparing for discharge (2);
  • provide consent and complete questionnaires independently (3);
  • no metastatic and second cancers (4);
  • using the Android smartphone (5).

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

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