Women treated for gynaecological cancer Cancer
Conditions
Interventions
Each participant will be randomly assigned to either an intervention group or a control group in a 1:1 ratio using block randomisation. Participants in the intervention group will receive a 12-week mu
and (ii) engage the participants to reflect on their belief, assumptions, knowledge and goals.
Participants in the control group will receive brief information on the follow-up schedule during baseli
Sponsors
Chinese University of Hong Kong
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Women with a primary diagnosis of gynaecological cancers (uterine, ovarian or cervical cancers) 2. Within 3 months of completion of intensive cancer treatments (e.g. surgery, radiotherapy, and /or chemotherapy) 3. Over 18 years old 4. Able to understand spoken Cantonese and to read Chinese 5. Having smartphones with iOS or Android operating systems 6. Consenting to participate
Exclusion criteria
Exclusion criteria: Those with unsuitable physical or mental health conditions, including visual impairment or preexisting psychosis, will be excluded as their ability to comprehend information and answer questionnaires would be affected.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sense of coherence measured using the Chinese version of the Sense of Coherence 13-item Scale (CSOC-13) at baseline, completion of the intervention, and 12 weeks after completion | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Cancer-specific distress measured using the Chinese version of the Impact of Events-Revised scale (CIES-R) at baseline, completion of the intervention, and 12 weeks after completion 2. Dietary and physical activity practices measured using the Chinese version of Health Promotion Lifestyle Profile II (HPLP-II) at baseline, completion of the intervention, and 12 weeks after completion 3. Health-related quality of life measured using the Chinese version of the Medical Outcomes Study (MOS) 36-item Short Form (SF-36) Health Survey at baseline, completion of the intervention, and 12 weeks after completion 4. Health-related quality of life measured using the Hong Kong version of the five-level EuroQol-5 Dimension (EQ-5D-5L) every three months from baseline to 12-month post-intervention 5. Participants' experiences, perceptions and opinions explored by semi-structured interviews upon completion of the intervention | — |
Countries
Hong Kong
Contacts
Public ContactKa Ming Chow
Outcome results
None listed