sability and initial efficacy testing of a website-delivered behaviour change intervention designed to promote physical activity among post-treatment breast cancer survivors.

Not Applicable

Completed

• Conditions: Breast Cancer; physical activity; Cancer - Breast; Public Health - Health promotion/education

• Registration Number: ACTRN12613001220752
• Lead Sponsor: Central Queensland University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2013-11-06
• Study Completion: 2015-03-02
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 492

Inclusion Criteria

To be eligible participants must:
Have previously been diagnosed with breast cancer (at any time point).
Have completed active cancer treatment (i.e., chemotherapy, radiotherapy, surgery).
Be proficient in the English Language in order to read content of the website and complete surveys.

Exclusion Criteria

To be eligible participants must not:
Have contraindications to exercise.
Participate in moderate-vigorous physical activity for 150 minutes or more per week.
Have previously participated in the Move More for Life Study (i.e., research project previously conducted by the research team).

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome, change in physical activity (Moderate-Vigorous mins/week) at 3 months post baseline, will be assessed using an adapted version of the leisure score index (LSI) of the validated Godin Leisure-Time Exercise Questionnaire (GLTEQ). The adapted version of the LSI contains three items assessing participants average participation (frequency and duration) in mild, moderate and strenuous aerobic physical activity in a typical week over the past month. [3 months post-baseline ]