FitARise: Making Exercise Advice and Referrals a Routine Part of Cancer Care
Official title: Implementation of the 3-steps Assess-Advise-Refer Exercise (FitARise) Protocol as a Standard Practice in Cancer Care: A Stepped-wedge Cluster Randomized Trial
Run by The University of Hong Kong · NCT07210905 · Data updated 2026-11-12
A program tests whether using structured steps to assess BMI, advise patients, and refer them to an exercise weight-management program can become a standard part of cancer care for eligible patients.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 1800 (estimated) |
| Sponsor | The University of Hong Kong Academic / other |
| Locations | 8 sites (Hong Kong and 7 other locations) |
| Status | Recruiting |
| Started | February 2, 2026 |
| Main results expected | February 2, 2027 |
| Study ends | February 2, 2028 |
| Registry record updated | August 27, 2026 |
| Trial ID | NCT07210905 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with cancer, BMI ≥ 23, within five years after completing treatment, literate in Chinese or English, and able to attend the exercise program.
✕Probably not a fit
Patients who do not meet BMI criteria, are outside the post-treatment window, or cannot attend the program may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This implementation study tests the FitARise protocol, which follows ASCM recommendations for exercise assessment, advice, and referral in routine cancer care. The study compares an implementation-strategy approach (audit, feedback, facilitation, and adaptable workflow) to a control condition where the protocol is available but not actively implemented. The primary outcome is the reach: the percentage of eligible patients who are assessed, advised, and referred based on BMI and treatment status. Qualitative methods will explore how clinicians and staff experience the implementation. Eligible participants are adults with cancer, BMI ≥ 23, within five years post-treatment, and literate in Chinese or English; eligible clinicians include oncologists at participating sites in Hong Kong.
Why it matters
Potential benefit: If successful, more patients who could benefit from exercise-based weight management will be assessed, advised, and referred in cancer care.
How similar studies have gone: Prior approaches to implementation of exercise guidelines in cancer care have shown mixed success, with this study addressing adoption strategies in a specific regional setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria (Cancer patients): * All cancer patients with BMI score\>=23; * Have completed cancer treatment within the past five years; * At least 18 years old; * Are literate in Chinese or English; * Are eligible to attend the intervention program. Exclusion Criteria (Cancer patients): * Patients who have completed cancer treatments for more than five years; * Non-Cantonese, non-Mandarin, non-English speakers. Inclusion Criteria (Clinical staff): \- All clinical, medical or surgical oncologists at the study units during the study period. Exclusion Criteria (Clinical staff): \- No exclusion criterial for staff.
Where it's running
-
KWH Department of Surgery
Hong Kong, Hong Kong Recruiting -
PMH Department of Oncology
Hong Kong, Hong Kong Recruiting -
PYEH Department of Clinical Oncology
Hong Kong, Hong Kong Recruiting -
QMH Department of Clinical Oncology
Hong Kong, Hong Kong Recruiting -
QMH Department of Obstetrics and Gynaecology
Hong Kong, Hong Kong Recruiting -
QMH Department of Surgery
Hong Kong, Hong Kong Recruiting
Show 2 more locations
-
TMH Department of clinical oncology
Hong Kong, Hong Kong Recruiting -
YCH Surgery Department
Hong Kong, Hong Kong Recruiting
Study contacts
- Principal investigator: Wendy Lam, PhD — The University of Hong Kong
- Study coordinator: Wendy Lam, PhD
- Email: wwtlam@hku.hk
- Phone: +852 39179878
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Gyrotonic exercise for elders with breast cancer and Behcet disease
We’re testing whether a gyrotonic exercise program helps older people who have both Behcet disease and breast cancer.
-
PECS II vs SPSIP nerve blocks for pain after mastectomy
This study tests whether two ultrasound-guided nerve blocks (PECS II and SPSIP) differ in how much opioid patients need after mastectomy.
-
CG-7321: a first-in-human test in advanced solid tumors
We’re testing CG-7321 alone and with fulvestrant to see if it’s safe and tolerable in adults with advanced solid tumors.
-
Compare a new endoscopy-assisted breast-conserving surgery with the usual approach
This study tests whether a new endoscopy-assisted breast-conserving technique can provide similar or better cosmetic outcomes and safety compared with conventional breast-conserving surgery in women with early breast cancer who want to preserve their breast.
-
Different skin care approaches to prevent skin reactions after mastectomy radiation
This study tests three standard skin care methods to see which best prevents radiation dermatitis in people who had a mastectomy and are receiving post-mastectomy radiation therapy.
-
3D Heart Strain to Detect Early Cardiotoxicity in Cancer Therapy
This study tests whether 3D echocardiography can detect early heart damage from cancer treatments like anthracyclines or HER2-targeted therapy better than standard 2D methods.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.