MedPath

A pragmatic randomised controlled trial to evaluate physical activity as a treatment for depressio

Completed
Conditions
Depression
Mild/moderate depression
Mental and Behavioural Disorders
Registration Number
ISRCTN16900744
Lead Sponsor
niversity of Bristol (UK)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
361
Inclusion Criteria

Patients aged 18-69 diagnosed by GPs as having a new episode of mild/moderate depression (ICD-10 diagnosis and a score of 14 or more on Beck Depression Inventory)

Exclusion Criteria

1. Physical contraindications to exercise
2. Inability to complete self-administered questionnaires
3. Psychosis
4. Serious drug or alcohol abuse
5. Pregnancy at time of randomisation

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Current primary outcome measures as of 10/04/2012:<br>Change in clinical symptoms of depression assessed using Beck Depression Inventory at 4-months post-randomisation.<br><br>Previous primary outcome measures:<br>Change in clinical symptoms of depression assessed using Beck Depression Inventory at 3-months post-randomisation.
Secondary Outcome Measures
NameTimeMethod
Current secondary outcome measures as of 10/04/2012:<br>A number of secondary outcomes will be measured at various points throughout the trial (4-months, 8-months, 12-months post-randomisation) including change in use of anti-depressants, uptake of physical activity, exercise efficacy and quality of life .<br><br>Previous secondary outcome measures:<br>A number of secondary outcomes will be measured at various points throughout the trial (3-months, 12-months, 24-months post-randomisation) including change in use of anti-depressants, uptake of physical activity, physical self-perceptions, exercise efficacy, psychiatric co-morbidity, quality of life and social support.
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