The effect of Moving On, a self management program for people with a chronic illness, on participants' self management knowledge, self efficacy and lifestyle behaviours.
- Conditions
- Coronary Heart Disease, Diabetes, Respiratory Illnesses, Asthma.Cardiovascular - Coronary heart diseaseMetabolic and Endocrine - DiabetesRespiratory - Asthma
- Registration Number
- ACTRN12609000298213
- Lead Sponsor
- niversity of New South wales
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 300
Consumers are eligible to join the study if (1) they are aged between 45-75yrs; (2) were not recently diagnosed with a chronic illness (provider determined); (3) have a reasonable understanding of their chronic ilness (provider determined); (4)are able to speak, write and understand english (provider determined); (5)agree to attend group education sessions (provider determined).
Consumers are not eligible to join the study if (1) they have been diagnosed with a severe mental illness (excluding depression and anxiety); (2) they have cognitive impairment issues including dementia; (3)they have substance abuse issues; (4) they are unable to participate in light physical activity.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in self efficacy (Stanford Self Efficacy for Managing Chronic Disease 6 Item Scale)[Measured at baseline and 4 months follow up];Change in self management knowledge and behaviour (Scales developed & previously piloted for the specific purposes of the trial)[Measured at baseline and 4 months follow up];Improvement in perceived health status (Stanford Self Rated Health Scale)[Measured at baseline and 4 months follow up]
- Secondary Outcome Measures
Name Time Method Improvement in work and social adjustment scores (Work and Social Adjustment Scale)[Measured at baseline and 4 months follow up];Greater knowledge concerning use of medicines (Scale developed & previously piloted for the specific purposes of the trial)[Measured at baseline and 4 months follow up];Improvement in anxiety and depression scores (Hospital Anxiety and Depression Scale)[Measured at baseline and 4 months follow up]