Randomized clinical trial that aims to increase physical activity levels in people with depression and to evaluate if the increase on PA levels has impact on clinical and biological measures.
The contacts will be made by face-to-face interviews and telephone calls
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
130
Pedometer: Each patient will receive a pedometer with increasing weekly aims on number of steps during the trial. The number of steps to be achieved starts on 4.000 and increases progressively until the end of the trial. Behavioral strategy based on STD theory, and the assessment of barriers and facilitators of each patient. All patients were receiving treatment as usual
Weekly call on general health aspects + treatment as usual
Hospital de Clínicas de Porto Alegre
Porto Alegre, Rio Grande do Sul, Brazil
RECRUITINGDepressive symptoms (blinded assessment)
Hamilton scale for depressive symptoms assessed by a blinded psychiatrist. Clinician-administered semi-structured interview with 17 questions. It is designed to measure the severity of depressive symptoms in patients with a primary depressive illness. Higher scores means higher depressive symptoms. The cutoffs are the following: following severity ranges for the HAMD: no depression (0-7); mild depression (8-16); moderate depression (17-23); and severe depression (≥24). The maximum score is 52.
Time frame: At the end of the intervention (6 months)
Physical activity - self-report
IPAQ
Time frame: At the end of the intervention (6 months)
Physical activity levels - objective measure
pedometer (only for intervention group)
Time frame: At the end of the intervention (6 months)
Quality of life
WHOQOL-BREF
Time frame: At the end of the intervention (6 months)
Depressive symptoms (self-reported)
Beck depressive inventory
Time frame: At the end of the intervention (6 months)
Melancholia
assessed using the CORE instrument
Time frame: At the end of the intervention (6 months)
Weight
Weight in kilograms
Time frame: At the end of the intervention (6 months)
PhD
CONTACT
Felipe Schuch, PhD
CONTACT
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