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The effect of positive thinking on stress, anxiety and depression

The effect of positive thinking on stress, anxiety and depression in coronary patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016022026347N2
Enrollment
60
Registered
2016-07-13
Start date
2015-12-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: Depression. Condition 2: anxiety. Condition 3: Coronary (artery):disease. Condition 4: stress. Depressive episode Generalized anxiety disorder Ischaemic heart diseases Acute stress reaction

Interventions

Intervention 1: Intervention: Positive thinking training In 8 sessions for 90 minute over 8 weeks. Intervention 2: control: No action.
Lifestyle
Intervention: Positive thinking training In 8 sessions for 90 minute over 8 weeks
control: No action

Sponsors

"Department of Technology and Scientific Research Urmia University of Medical Science"
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria interested in participating in research studies at least grade;Minimum education guidance;Age 65-20 years; The definitive diagnosis of coronary heart disease by cardiologists and vascular;business written informed consent from subjects Exclusion criteria Attend classes simultaneously ; drug treatment of other sedatives, anti-anxiety, anti-depression drug and ;having chronic diseases (progressive Neurologic Diseases such as Parkinson's, Alzheimer's, multiple sclerosis, cancer and diabetes) ; psychological disorders ; being under open-heart surgery;an unwillingness to cooperate in the investigation in any time of the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression. Timepoint: Before the intervention, two weeks after the intervention. Method of measurement: Standard questionnaire.;Stress. Timepoint: Before the intervention, two weeks after the intervention. Method of measurement: Standard questionnaire.;Anxiety. Timepoint: Before the intervention, two weeks after the intervention. Method of measurement: Standard questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNiloofar Oladrostam

niversity of Medical Sciences

baran_sahra65@yahoo.com+98 44 4552 2875

Outcome results

None listed

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