eMindExCare for Prostate Cancer Patients Undergoing Active Treatment

Starting soon · Not applicable

Conditions studied: Prostate Cancer, Sleep Disturbance, Fatigue, Physical Inactivity, Pain

In brief

This feasibility randomized controlled trial will assess the acceptability, feasibility, and preliminary effects of an integrated mindfulness and exercise eHealth intervention, eMindExCare, among prostate cancer patients undergoing active treatment in Hong Kong. Participants will be randomized in a 1:1 ratio to either an 8-week eMindExCare intervention or an enhanced health education attention-control programme. eMindExCare integrates culturally adapted Cantonese mindfulness practices with home-based aerobic and resistance exercise delivered through Zoom, supported by home practice, exercise logs, and weekly reminders. The enhanced health education control programme will match the intervention group in contact time and engagement but will not include progressive aerobic training, resistance-band prescription, stationary bike provision, or a structured mindfulness curriculum. Feasibility and acceptability outcomes will include eligibility, consent, randomization, attendance, retention, questionnaire completion, missing data, and adverse events. Preliminary outcomes will include sleep quality, fatigue, pain, physical activity, mindfulness, motivation for exercise, and quality of life assessed at baseline, immediately post-intervention at week 8, and 3 months post-intervention.

Key facts

Study ID

NCT07735273

Run by

The University of Hong Kong

People needed

60

Starts

2026-10-01

Expected to finish

2028-09-30

Last updated by the study team

2026-07-29

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Diagnosed with prostate cancer, stage I, II, or III.
• Aged older than 18 years.
• Undergoing active treatment, including chemotherapy, radiotherapy, or hormone therapy, at Prince of Wales Hospital.
• Able to communicate and read Chinese.
• Has access to the Internet and a computer or tablet.
• Demonstrates clinically impaired sleep quality or insufficient physical activity as measured by ActiGraph. Clinically impaired sleep quality may include study-defined sleep disturbance criteria such as total sleep time less than 6.5 hours, sleep onset latency greater than 30 minutes, awakenings lasting greater than 5 minutes, or wake after sleep onset greater than 30 minutes.

You may not qualify if…

• Diagnosed with more than one primary cancer.
• Has metastatic disease.
• Has participated in a mindfulness programme.
• Is sufficiently physically active at the time of recruitment.
• Has a mental condition, World Health Organization/Eastern Cooperative Oncology Group performance status greater than 2, a physical disability that prevents participation in the intervention, or any other health problem that rules out regular physical activity as determined by the treating physician.

Where it is running

• Prince of Wales Hospital, Urology Division — Hong Kong, Hong Kong

Full record on ClinicalTrials.gov

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