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The effect of aerobic exercise on depression

Effect of Indoor and Green Aerobic Exercise Compared with Psychotherapy on Reducing Depression in the Patients with Major Depressive Disorder: An Investigation of Psycho physiological Mechanisms of Stress and Coping

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016082929598N1
Enrollment
72
Registered
2016-12-05
Start date
2014-06-07
Completion date
Unknown
Last updated
2018-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severe depressive episode. Severe depressive episode without psychotic symptoms

Interventions

Intervention 1: Indoor aerobic exercise program: Besides usual pharmacotherapy this group will use 60 min of group aerobic exercise accompanied by rhythmic music with a schedule of three sessions per

Sponsors

Psychiatric Clinic of Bahman Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1- The women aged 20-50-years; affected with moderate to severe major depressive disorder diagnosed by a psychiatrist via structured clinical interview based on the fifth version of the diagnostic and statistical manual of mental disorders (DSM-5) (American Psychiatric Association, 2013), and the minimum score of 20 on the Beck Depression Inventory–II (Beck, Steer, & Brown, 1996). 2- Not being involved in other mental treatments and exercise programs during the study. 3- Declare her willingness to take part in the research and sign the informed consent statement.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1- Simultaneous affliction with other important mental disorders (such as schizophrenia, bipolar affective disorder and drug and alcohol abuse). 2- Having somatic problems affecting depression (such as hypothyroidism and diabetes mellitus). 3- Having somatic problems restricting physical activity (e.g., cardiovascular and musculoskeletal problems).

Design outcomes

Primary

MeasureTime frame
Depression. Timepoint: Once before and once after the intervention (three months later). Method of measurement: Beck Depression Inventory-II.

Secondary

MeasureTime frame
Perceived Stress. Timepoint: Once before and once after the intervention (three months later). Method of measurement: The Persian version of the 10-item Perceived Stress Scale (PSS-10) (Cohen, Kamarck, & Mermelstein, 1983).;Blood Cortisol. Timepoint: Once before and once after the intervention (three months later) between 8-9 a.m. Method of measurement: Enzyme-Linked Immunosorbent Assays (ELISA) with the Monobind Kit, made in USA.;Coping Strategies. Timepoint: Once before and once after the intervention (three months later). Method of measurement: The Persian version of Coping Inventory for Stressful Situations (CISS).;Quality of life. Timepoint: Once before and once after the intervention (three months later). Method of measurement: The Persian version of World Health Organization Quality of life-BREF (WHOQOL-BREF), (Quality of life Group, World Health Organization, 1996).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJafar Askari

Shahid Sadoughi University of Medical Sciences

askarifarr@gmail.com+98 35 3820 3410

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026