Promotion of physical activity in breast and prostate cancer survivors
Recruiting
- Conditions
- Breast and Prostate CancerPhysical ActivityFatiqueMoodHealth related Quality of life.Borst en ProstaatkankerFysieke activiteitVermoeidheidStemmingsklachtenGezondheidsgerelateerde kwaliteit van leven.
- Registration Number
- NL-OMON26518
- Lead Sponsor
- Antoni van LeeuwenhoekRijnstate
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 246
Inclusion Criteria
Histologically confirmed primary breast or prostate cancer (stages: T1 - T4, NO - N3 and M0)
-Primary treatment should have been completed a minimum of 3 months and a maximum of 12 months prior to study entry.
Exclusion Criteria
-Patients who are unable to or cannot safely perform unsupervised exercise at the at the recommended levels.
-Patients who lack basic proficiency in Dutch.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measure is change in minutes of weekly moderate to vigorous physical activity from baseline to 6 and 12 months as assessed by accelerometer.
- Secondary Outcome Measures
Name Time Method The secondary outcomes are: self-reported physical activity (IPAQ). Stage of change, fatigue (MFI) mood (POMS), HRQOL (SF-36, EQ5D) and will be assessed by questionnaires.At baseline, 6 and 12 months. Medical consumption (iMCQ) and productivity costs (iPCQ) will be measured at 6 and <br>12 months by questionnaire.