Actively Recruiting
How to Prevent Lost in Transition? Adaptive Randomised Controlled Trial of a Self-management Based Survivorship Intervention for Chinese Cancer Survivors
Led by The University of Hong Kong · Updated on 2025-05-13
486
Participants Needed
7
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a cancer survivorship care intervention designed to help Chinese patients who have recently finished curative cancer treatment. This study uses a sequential multiple assessment randomized controlled trial (SMART) to assess how the intervention affects physical symptom distress, weight management, self-confidence in managing cancer, and overall health-related quality of life. The trial compares different approaches to survivorship care to find better ways to support patients after treatment. Participants are divided into groups receiving different types of support. One group attends a 120-minute survivorship clinic with a team including a nurse, dietitian, exercise physiologist, and psychologist, where they get personalized advice on symptom management, diet, exercise, and psychosocial issues. Another group receives skill-based pamphlets covering symptom management and lifestyle recommendations. Some participants who continue to struggle with symptoms or weight after initial care may receive a more personalized, step-up intervention focused on coaching to improve symptom relief and weight control. During the study, participants will be assessed at baseline and again at 4 and 12 months. Researchers will measure symptom distress, weight control, self-efficacy, fear of cancer recurrence, illness perception, and health-related quality of life. Participants will be monitored to see how their symptoms and quality of life change over time, helping to understand which care approaches work best. The total study period extends to the end of 2026, including follow-up assessments to track long-term effects.
CONDITIONS
Brief Title
A Self-management Based Survivorship Intervention for Chinese Cancer Survivors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Cantonese- or Mandarin-speaking Chinese patients diagnosed with curable cancer
- Completed primary and adjuvant treatment within the past six months
- Adults aged 18 years or older
You will not qualify if you...
- Patients diagnosed with metastatic cancer
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants receive either a one-off face-to-face assessment with personalized advice from a multidisciplinary team in a cancer survivorship clinic or a set of skill-based self-management pamphlets addressing symptom management and lifestyle recommendations.
1 baseline visit (in-person)
Duration - Up to 8 months
Participants who continue to have symptom distress or suboptimal weight control after the initial intervention may receive a step-up targeted personalized intervention focusing on symptom management and weight control, or continue following the advice given in the initial visit or pamphlets.
Follow-up visits up to 12 months post-baseline with assessments at 4 months and 12 months
Trial Site Locations
Total: 7 locations
1
Kwong Wah Hospital-Breast Center
Hong Kong, Hong Kong
Active, Not Recruiting
2
Pamela Youde Nethersole Eastern Hospital-Department of oncology
Hong Kong, Hong Kong
Active, Not Recruiting
3
Prince of Wales Hospital-Department of Surgery
Hong Kong, Hong Kong
Active, Not Recruiting
4
Queen Mary Hospital-Department of Obstetrics & Gynaecology
Hong Kong, Hong Kong
Actively Recruiting
5
Queen Mary Hospital-Department of Oncology
Hong Kong, Hong Kong
Actively Recruiting
6
Queen Mary Hospital-Department of Surgery
Hong Kong, Hong Kong
Actively Recruiting
7
Tung Wah Hospital-Department of Surgery
Hong Kong, Hong Kong
Active, Not Recruiting
Research Team
W
Wendy Wing Tak Lam, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
TREATMENT
Number of Arms
4
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