Women treated for gynecological cancer Cancer Malignant neoplasms of female genital organs
Conditions
Interventions
The enrolled subjects were randomized in a 1:1 ratio into intervention group or control group after baseline data collection. Sealed envelopes were used to ensure allocation concealment. Group allocat
new information was posted on the website every day in the first three weeks, and then weekly for the following nine weeks. Participants’ click-through rates were monitored and follow-up telephone cal
Sponsors
Chinese University of Hong Kong
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Chinese women diagnosed with cervical, ovarian, uterine, vaginal, or vulva cancer as a primary cancer and have completed treatment 2. Aged =18 years 3. Able to comprehend Chinese and communicate in Cantonese 4. In possession of a tablet computer or smartphone
Exclusion criteria
Exclusion criteria: Unsuitable physical or mental health conditions, including visual impairment or pre-existing psychosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Health-related quality of life measured using the Traditional Chinese version of the Functional Assessment of Cancer Therapy-General Version 4 at baseline, immediately post-intervention, and 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Depression and anxiety measured using the Chinese version of the Hospital Anxiety and Depression Scale at baseline, immediately post-intervention, and 12 weeks 2. Self-efficacy in adhering to a healthy diet measured using the Chinese version of Bandura’s Eating Habits Self-Efficacy scale at baseline, immediately post-intervention, and 12 weeks 3. Self-efficacy in adhering to an exercise routine measured using the Chinese version of Bandura’s Exercise Self-Efficacy scale at baseline, immediately post-intervention, and 12 weeks | — |
Countries
Hong Kong
Contacts
Public ContactKa Ming Chow
Outcome results
None listed