Topic: Cancer
Conditions
Interventions
ASCOT is a lifestyle intervention (a leaflet developed in consultation with clinicians and patients, a phone consultation and a website) aimed at helping cancer patients adhere to the World Cancer Res
Sponsors
University College London Joint Research Office
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Current inclusion criteria as of 18/12/2020: ASCOT patient survey: All individuals diagnosed with breast, prostate or colorectal cancer in 2012-2015 at an NHS trust in London or Essex. ASCOT pilot trial: 1. Adults aged at least18 years (no upper age limit) 2. Individuals diagnosed with non-metastatic breast, prostate or colorectal cancer in 2012-2015 3. Individuals not receiving active anti-cancer treatment (except for those oral anti-cancer treatments taken at home who can be included) 4. Individuals who are able to understand spoken and written English Previous inclusion criteria: ASCOT patient survey: All individuals diagnosed with breast, prostate or colorectal cancer in 2012 or 2013 at an NHS trust in London or Essex. ASCOT pilot trial: 1. Adults aged at least18 years (no upper age limit) 2. Individuals diagnosed with non-metastatic breast, prostate or colorectal cancer in 2012 or 2013 3. Individuals not receiving active anti-cancer treatment (except for those oral anti-cancer treatments taken at home who can be included) 4. Individuals who are able to understand spoken and written English
Exclusion criteria
Exclusion criteria: ASCOT pilot trial: 1. Individuals with metastatic disease 2. Individuals on active anti-cancer treatment requiring hospital admission 3. Individuals with severe cognitive impairment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Current primary outcome measures (as of 10/01/2018) Composite health behaviour risk index; Timepoint(s): 0, 3, 6 and 24 months Previous primary outcome measures Composite health behaviour risk index; Timepoint(s): 0, 3 and 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Current secondary outcome measures (as of 10/01/2018) 1. Alcohol (AUDIT C questionnaire); Timepoint(s): 0, 3, 6 and 24 months 2. Dietary intake (24 hour dietary recall phone calls); Timepoint(s): 0, 3, 6 and 24 months 3. Physical activity (pedometer and questionnaire); Timepoint(s): 0, 3, 6 and 24 months 4. Quality of Life (EQ-5D-5L); Timepoint(s): 0, 3, 6 and 24 months 5. Sleep (questionnaire); Timepoint(s): 0, 3, 6 and 24 months 6. Smoking status (questionnaire); Timepoint(s): 0, 3, 6 and 24 months Previous secondary outcome measures 1. Alcohol (AUDIT C questionnaire); Timepoint(s): 0, 3 and 6 months 2. Dietary intake (24 hour dietary recall phone calls); Timepoint(s): 0, 3 and 6 months 3. Physical activity (pedometer and questionnaire); Timepoint(s): 0, 3 and 6 months 4. Quality of Life (EQ-5D-5L); Timepoint(s): 0, 3 and 6 months 5. Sleep (questionnaire); Timepoint(s): 0, 3 and 6 months 6. Smoking status (questionnaire); Timepoint(s): 0, 3 and 6 months | — |
Countries
England, United Kingdom
Contacts
Public ContactRebecca Beeken
Outcome results
None listed