Clinical trial · Interventional
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
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Colorectal Cancer (Diagnosis) | Malignant Colorectal Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Intervention Group | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- NO_INTERVENTION
- label
- Control group
- description
- Participants in the control group will receive the usual care
- type
- ACTIVE_COMPARATOR
- label
- mHealth survivorship program
- description
- 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
- interventionNames
- Other: Intervention Group
Primary outcomes (1)
- measure
- The Functional Assessment of Cancer Therapy-General (FACT-G)
- timeFrame
- Participants will be assessed at three-time points: baseline (Day 1), post-intervention (12 weeks), and 1-month follow-up (after post intervention))
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * 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). Exclusion Criteria: * mental health diseases; * receiving anxiety or depression treatment or cognitive/learning problems.
References
Publications (0)
Data not yet available