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The impact of physical activity promotion by health professionals on physical activity levels of adults & young people receiving outpatient care (PROMOTE-PA study)

Not Applicable
Conditions
Public Health - Other public health
Physical inactivity
Physical Medicine / Rehabilitation - Other physical medicine / rehabilitation
Registration Number
ACTRN12623000920695
Lead Sponsor
The University of Sydney
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
720
Inclusion Criteria

Health professional participants
-A health professional providing outpatient or community- based clinical services within a participating clinical service in SWSLHD, SLHD, SCHN, SESLHD, WSLHD or within NSW private outpatient physiotherapy practice or specialist medical service.
-Health professionals who have the scope to include physical activity promotion in their practice, including physiotherapists, occupational therapists, geriatricians, rehabilitation physicians, rheumatologists, endocrinologists, surgeons, sports physicians, exercise physiologists and nurses.
-Willingness to provide informed consent and willingness to participate and comply with the study requirements.

Patient participants
-Adults or school-aged children living in the community who are attending a participating clinical service and who are willing to receive additional support to be more physically active.
-No contra-indications to increase PA.
-Sufficient language capabilities to respond to written or verbal questionnaires in English, Arabic or Vietnamese.

Exclusion Criteria

Health professional participants
•Health professionals who are not working in relevant clinical areas outlined above.
Patient participants
•Participants who have a medical condition precluding physical activity/exercise
•Insufficient language capabilities to respond to written or verbal questionnaires in English, Arabic or Vietnamese
•Progressive neurological disease that severely affects function
•Other e.g., delirium, severe psychiatric disorders

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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