Colorectal surgery Cancer
Conditions
Interventions
Recover Together intervention comprising of:
1. Recover Together booklet
2. Recover Together video
3. Recover Together goal board
The total duration of the intervention is 3 months.
Sponsors
University of Leeds
Eligibility
Sex/Gender
All
Age
18 Years to 110 Years
Inclusion criteria
Inclusion criteria: To be eligible for the study, patients must satisfy all of the following inclusion criteria: 1. Aged >= 18 years 2. Able to provide written informed consent 3. Planned to undergo elective colorectal surgery (with or without a stoma) 4. Indication for surgery is for suspected or confirmed colorectal cancer For the staff interviews, we will include staff who have experience of introducing the video and booklet in outpatient clinics, and/or delivering the goal board on the ward, as well as staff who have trained other staff in how to deliver the intervention.
Exclusion criteria
Exclusion criteria: No further exclusion criteria will apply although participants will be required to understand either English or Urdu language. There will be no exclusions based on literacy or disability.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intervention feasibility measures: 1. Time taken for intervention set up across participating sites measured according to time from HRA approval to first enrolment 2. Compliance with core processes per resource measured according to the proportion of core processes satisfied per resource 3. Compliance with all core processes per participant measured according to the proportion of all core processes satisfied Study method feasibility measures: 1. Return rate per measurement instrument measured according to the rate of return per instrument 2. Return rate of all instruments per participant measured according to the overall rate of return per participant 3. Rate of missing cost/resource utilisation data measured according to the rate of missing data points All of the feasibility endpoints are measured once at the end of the study | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical instrument measures: 1. Patient satisfaction measured using the Bauer Patient Satisfaction Questionnaire on Day 1 after surgery 2. Patient well-being measured using the Quality of Recover-15 survey at baseline and on Day 3 after surgery 3. Health-related quality of life measured using the EQ-5D-5L at baseline, Day 30, and 6 months after surgery 4. Functional status measured using the WHO Disability Assessment Schedule 2.0 at baseline and 6 months after surgery 5. Resource use using a bespoke resource-use questionnaire measured at baseline and 6 months after surgery | — |
Countries
England, United Kingdom
Outcome results
None listed