Breast cancer/cancer screening/cancer prevention Cancer Malignant neoplasm of breast
Conditions
Interventions
Participants were randomised (1:1) to either the ActWELL intervention or usual care (booklet only).
The ActWELL intervention consisted of a 1-hour counselling session (face to face) with a lifestyle
Sponsors
Tayside Medical Science Centre (UK)
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Participation in the NHS breast cancer screening programme (age range 50 ? 75 years)
Exclusion criteria
Exclusion criteria: 1. Breast cancer diagnosis 2. BMI < 20 kg/m2 3. Any known contra-indicators to physical activity or weight management
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Feasibility outcomes - programme implementation, fidelity to protocol, achieved measurements, recruitment, response, early retention and reported adherence. Acceptability measures of recruitment, implementation and exit strategy (i.e., signposting to further support) 2. Indicative findings - primary outcome was weight change, measured at baseline and follow up (after 3 months) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Indicative findings measured at baseline and follow up (after 3 months): 1.1. Changes in waist circumference 1.2. Changes in blood pressure 1.3. Changes in physical activity (International Physical Activity Questionnaire Short form) 1.4. Changes in diet and alcohol habits (dietary instrument for nutrition education, 24 h diet recall, 7-day alcohol record) | — |
Countries
United Kingdom
Outcome results
None listed